Longitudinal relationship of amino acids and indole metabolites with long-term body mass index and cardiometabolic risk markers in young individuals

Abstract

Amino acid metabolites in biofluids are associated with high body mass index (BMI) and cardiometabolic abnormalities. However, prospective investigations regarding these associations are few, particularly among young individuals. Moreover, little is presently known about the impact of long-term high BMI. Using data from the DOrtmund Nutritional and Anthropometric Longitudinally Designed study (111 males and 107 females), we prospectively investigated relations between repeatedly measured urinary levels of 33 metabolites and (1) previously identified long-term BMI trajectory groups from childhood into late adolescence and (2) cardiometabolic risk markers in late adolescence–young adulthood, in sex-specific linear mixed regression models. Males with long-term overweight had lower indole-3-acetic acid when compared to others. Further, methionine, isoleucine, tryptophan, xanthurenic acid, and indole-3-carboxaldehyde were negatively associated with C-reactive protein (CRP), but 5-hydroxyindole-3-acetic acid was positively associated with CRP. No associations were observed in females. Long-term overweight from childhood into late adolescence is associated with decreased urinary levels of gut bacteria-derived indole-3-acetic acid, and several urinary amino acids, including gut bacteria-derived indole-3-carboxaldehyde are associated with elevated CRP later on in life. Taken together, our data suggest that indole metabolites, and their gut bacteria producers play potentially important roles in overweight-related inflammation.

Introduction

High body mass index (BMI) during childhood and adolescence is still a major public health concern1,2. The condition contributes to the development of cardiometabolic abnormalities such as inflammation over the life course3. Dysregulated metabolism is one of the biological mechanisms through which high BMI contributes to the development of these cardiometabolic abnormalities4,5. Scientific efforts have focused on carbohydrate and lipid metabolic perturbations as one of these mechanisms, interest in the impact of unfavorable alterations in protein/amino acid metabolism is now emerging6,7. Therefore, it would be necessary to explore the link of high BMI, amino acid metabolites, and cardiometabolic abnormalities.

Epidemiological studies in children and adolescents have reported positive association between BMI and biofluid amino acid and/or their metabolites such as alanine8,9, valine8,9,10, leucine8,10,11, isoleucine8,10,11, phenylalanine8,11, tyrosine8,9,11, histidine8, cysteine12, tryptophan-derived metabolites13, kynurenic acid9,11, kynurenine11, the kynurenine to tryptophan ratio (KTR, an index of increased metabolism of tryptophan along the kynurenine pathway)14, lysine, methionine, γ-glutamyltyrosine, asparagine, glycine, serine11, and branched-chain amino acids15. Conversely, negative association between BMI and leucine, isoleucine, phenylalanine, arginine, histidine, serine, and citrulline4, glutamine9, indole-3-propionic acid16, and 5-hydroxyindole acetic acid17 are also documented. Some of these findings are restricted to males14,17. These BMI-related changes in amino acid profiles might be a consequence of higher or lower intake of specific protein-containing foods18, changes in the activities of catabolizing host and/or bacterial enzymes18,19, changes in the redox status of the adipose tissue and liver19, and down-regulation of the expression of adipose tissue amino acid metabolizing enzymes and uptake of amino acids by adipose tissue20.

Similarly, amino acid metabolites are positively related to cardiometabolic risk markers (CRM) in children, adolescents, and young adults, albeit with a few exceptions. The positive associations include branched-chain amino acids (BCAAs) with insulin resistance (IR)15,21,22, triglycerides23, and triglycerides to high-density lipoprotein-cholesterol (HDL-C) ratio24; valine, leucine, and isoleucine10, phenylalanine and tyrosine21, and kynurenine and KTR25 with IR; cysteine with fasting plasma glucose (FPG), leptin, and IR;12 indole-3 propionic acid with HDL-C16; arginine, histidine, and serine with insulin sensitivity5; KTR with C-reactive protein (CRP), interferon-gamma, interleukin (IL)−6, IL-10, and alpha-1-acid glycoprotein26; and isoleucine and valine with IR27. The few reported negative associations include BCCAs with FPG23 and adiponectin24; tryptophan with CRP, interferon-gamma, IL-6, IL-10, and alpha-1-acid glycoprotein26; and numerous amino acids with CRP and IL-628. The relation of BCCA with BCCAs with FPG23 and adiponectin24, and that of isoleucine and valine with IR27 are restricted to males, while the relation of BCAA with triglycerides23, and triglycerides to HDL-C ratio24 are restricted to females. The mechanistic involvement of BCCAs in the development of IR includes persistent activation of mTOR signaling pathway and accumulation of toxic BCAA metabolites that trigger mitochondrial dysfunction29, and the involvement of tryptophan and KTR in inflammation is through the immunoregulatory role of indoleamine 2,3-dioxygenase 130.

Notably, only a few of the aforementioned studies are prospective9,21,24,25,26. Thus, more prospective investigations are needed. Moreover, the one-time measurement of BMI in earlier studies indicate a relation between a static state of body composition and amino acid metabolites. Given that body composition is dynamic, particularly among children and adolescents31, it would be necessary to investigate whether long-term BMI is associated with similar or different amino acid metabolites. Moreover, our knowledge of the relation between BMI and amino acid metabolites, and between amino acid metabolites and CRM might be incomplete because earlier studies sampled amino acids only at one time point. Static sampling of amino acids does not adequately capture the complex interplay of the several phases of host metabolism19. Further, some findings being restricted to either males or females warrants sex-specific analysis. Surely, aberrant amino acid metabolites may reveal metabolites and/or metabolic pathways perturbed as a result of a high BMI and identification of amino acids related to CRM may improve our understanding of the pathophysiological mechanisms underlying cardiometabolic abnormalities.

In a group of apparently healthy young individuals in whom BMI was measured annually over a 15-year period from childhood to late adolescence, we previously identified distinct long-term BMI trajectory groups32. In a subset of this study sample, we therefore sought in sex-specific analysis to (1) examine association between long-term BMI trajectory groups and repeatedly measured urine metabolites, mostly amino acids, during childhood and adolescence, and (2) investigate whether these metabolites are prospectively associated with the levels of 11 CRM in late adolescence–young adulthood.

Results

Study population

Our study population comprised 111 males and 107 females. As published before32, overweight trajectory was present only in males, and more males followed the high-normal weight trajectory as compared to females. Urine was sampled in majority of individuals at ages 9, 17, 18. In late adolescence–young adulthood, males had higher levels of SBP and FPG, while females had higher HDL-C, CRP, adiponectin, chemerin, and leptin. Males were heavier and longer than females at birth, males consumed more energy and protein daily as compared to females, and a lower percentage of mothers of males were employed as compared to mothers of females (Table 1).

Table 1 Basic characteristics of the study population, 111 males and 107 females.

Further details of the study participants’ age at urine sampling (metabolite measurement) are shown in Suppl. Table 1a,b. In both sexes, over half of the participants had their three measurements at ages 9, 17, and 18, and about 10% had measurements at ages 9, 16, and 17.

Multivariable linear regression

The association between BMI trajectory and metabolites

As shown in Suppl. Table 2, except for kynurenine and KTR in males, the linear time models yielded generally a better fit for the metabolites. Therefore, except for these two metabolites which we fitted with quadratic time models, all the remaining metabolites in both sexes were fitted with linear time models.

Table 2 shows the p-values and q-values of the association between BMI trajectory group and each of the 32 metabolites and KTR in males and females. The results indicate that at p-value ≤ 0.05 and q-value ≤ 0.05, BMI trajectory group was significantly associated with 3-methoxy-p-tyramine (p-value = 0.005, q-value = 0.045), indole-3-acetamide (p-value = 0.005, q-value = 0.045), and indole-3-acetic acid (p-value = 0.0001, q-value = 0.002) in males. However, BMI trajectory group was not associated with any metabolites in females. For this reason, subsequent mean comparisons were performed for only 3-methoxy-p-tyramine, indole-3-acetamide, and indole-3-acetic acid in males.

Table 2 The p-values and q-values of the association of body mass index trajectory group with 32 metabolites and kynurenine to tryptophan ratio in males and females.

The results of the marginal mean difference in standard-deviation (SD) scores of 3-methoxy-p-tyramine, indole-3-acetamide, and indole-3-acetic acid between the BMI trajectory groups in males are shown in Fig. 1. Adjusting for time (model 1), the overweight and high-normal weight trajectory groups had lower 3-methoxy-p-tyramine as compared to the mid-normal weight trajectory group. The overweight trajectory had lower indole-3-acetamide and indole-3-acetic acid as compared to all remaining three trajectory groups. Additionally, the high-normal weight trajectory group had lower indole-3-acetic acid as compared to the mid-normal weight trajectory group (Fig. 1, left). After full covariate adjustment (model 2), the overweight trajectory had 0.54 SD, 0.83 SD, 0.67 SD lower indole-3-acetic acid as compared to the high-normal weight (−0.54: −1.04; −0.033, adjusted p-value =  0.033), mid-normal weight (−0.83: −1.33; −0.32, adjusted p-value =   < 0.001), and low-normal weight (−0.67: −1.22; −0.11, adjusted p-value =  0.012) trajectory groups, respectively (Fig. 1, right).

Figure 1
figure1

Mean difference in standard-deviation scores of 3-methoxy-p-tyramine, indole-3-acetamide, and indole-3-acetic acid between pairs of body mass index trajectory groups in males. Model 1: left, Model 2: right. Model 1: adjusted for time. Model 2: adjusted for time, birth weight and length, maternal BMI, maternal pregnancy weight gain, breastfeeding duration, birth order, maternal education, and maternal employment, smoking in household, physical activity, daily energy intake, percentage of energy from protein, and two-way interactions of physical activity, daily energy intake, and percentage of energy from protein with BMI trajectory. *Simulated adjusted p-value.

In humans, ultimate source of indole-3-acetic acid is tryptophan. Hence, in sensitivity analyses, BMI trajectory group differences in indole-3-acetic acid were further adjusted for tryptophan. Adjusting for this precursor slightly attenuated the above result (Suppl. Table 3). This result was similar with further adjustment for urine creatinine or osmolality.

The association between metabolites and kynurenine and tryptophan ratio, and cardiometabolic risk markers

Collectively, the metabolites and KTR explained between 26–54% and 10–89% of the variance in CRM in males and females, respectively (Table 3). However, at p-value ≤ 0.05 and q-value ≤ 0.05 only the explained variance of CRP in males was statistically significant. The metabolites and KTR collectively explained 54% of the variance in CRP in males (p-value = 0.002, q-value = 0.025). Therefore for subsequent analysis, we reported associations between these metabolites and CRP in males.

Table 3 Overall significance of regression model with cardiometabolic risk markers as dependent variable and 32 metabolites and kynurenine and tryptophan ratio as independent variables.

As shown in the model comprising only the metabolites (model 1), methionine, isoleucine, picolinic acid, tryptophan, xanthurenic acid, and indole-3-carboxaldehyde were negatively associated with CRP, but 5-hydroxyindole-3-acetic acid was positively associated with CRP (Fig. 2, left). Following full covariate adjustment (model 2), a 1 SD increase in methionine (β = −0.70: −1.29; −0.12, p-value = 0.02), isoleucine (β = −2.03: −3.48; −0.59, p-value = 0.007), tryptophan (β = −2.74: −5.30; −0.17, p-value = 0.037), xanthurenic acid (β = 1 = −0.90: −1.62; −0.18, p-value = 0.015), and indole-3-carboxaldehyde (β = −0.53: −1.00; −0.06, p-value = 0.029) were associated with a 0.7 SD, 2 SD, 2.7 SD, 0.9 SD, and 0.5 SD decrease in CRP, respectively. Further, a 1 SD increase in 5-hydroxyindole-3-acetic acid (β = 1.26: 0.51; 2.01, p-value = 0.001) was associated with a 1.3 SD increase in CRP (Fig. 2, right). Indole-3-carboxaldehyde has the narrowest 95% CI, therefore its significant association with CRP has the least uncertainty. These results were essentially unaltered following additional adjustment for urine creatinine or osmolality.

Figure 2
figure2

Association of 32 metabolites and kynurenine to tryptophan ratio with CRP in males. Model 1: left, Model 2: right. Model 1 comprises all 32 metabolites and kynurenine and tryptophan ratio. Model 2 was Model 1 adjusted for birth weight and length, maternal BMI, maternal pregnancy weight gain, breastfeeding duration, birth order, maternal education, and maternal employment, smoking in household, physical activity, daily energy intake, percentage of energy from protein, and BMI trajectory. *Multivariable adjusted p-value.

Discussion

The aims of this study were to examine sex-specific associations between long-term BMI trajectory groups and repeatedly measured urine metabolites, mostly amino acids, among apparently healthy young individuals, and to investigate whether these metabolites are associated with the levels of subsequent CRM in late adolescence–young adulthood. We observed that individuals who belonged to the overweight trajectory group, that is, persistently overweight from childhood into late adolescent had lower levels of urinary indole-3-acetic acid when compared to other individuals. Furthermore, we found that methionine, isoleucine, tryptophan, xanthurenic acid, and indole-3-carboxaldehyde levels were independently negatively, and 5-hydroxyindole-3-acetic acid levels were independently positively associated with CRP in late adolescence–young adulthood. Interestingly, both findings were restricted to males.

Our sex-specific findings extends previous findings of studies in children and adolescents comprising both sexes. This includes a study reporting that high BMI was associated with a decreased KTR in males, but not in females14. Moreover, BCCAs were associated with a decreased FPG in males, but increased triglycerides in females23 as well as with a decreased adiponectin in males, but with increased triglycerides to HDL-C ratio in females24. The fact these studies14,23,24 and ours consistently showed inverse associations in males suggest that our findings are unlikely to be spurious. Possible explanations for these observed sex-specific findings include sex-related differences in protein turnover, amino acid handling systems, and the influence of sex hormones33. Sex-related differences are thought to primarily develop after adolescence due to the more marked hormonal differences33. However, considering that our study included measurement of metabolites in childhood, either indicate that an impact of sex hormones occur before adolescence, or that all the aforementioned mechanisms provide a complete explanation of the sex-specific findings. These sex-specific findings warrant further investigation.

Overweight, either cross-sectionally or prospectively has not been previously linked to indole-3-acetic acid in children and adolescents. The few cross-sectional studies in adults regarding indole-3-acetic acid have yielded mixed results34,35,36,37. In agreement with our study, Liu et al. observed that BMI negatively correlated with sputum indole-3-acetic acid35, a result at variance with others in which no relation was observed between BMI and serum indole-3-acetic acid34, between BMI and faecal indole-3-acetic acid36, and between BMI and plasma indole-3-acetic acid in older men37. Clearly, BMI trajectory group differences being observed for only indolic tryptophan metabolite indicate that the impact of long-term BMI is very specific and does not result in a global disruption of all amino acid metabolism. However, our study failed to demonstrate an association with indole-3-propionic acid, an indole metabolite that has been cross-sectionally related to BMI in children and adolescents16. Indeed, the consistent inverse relation of BMI with the indole metabolites in our study and Farook et al.16 suggest that high BMI impact indolic tryptophan metabolism, with the resulting metabolites being dependent on the duration of high BMI. Indole-3-acetic acid have been shown to drive the emergence of obesity by acting on the extended reward network36, however the current study modeled the effect of BMI trajectory group since it makes intuitive sense that changes in BMI impacted the levels of indole-3-acetic acid and our BMI measurements precedes metabolite measurements. Nonetheless, one cannot exclude the presence of a bidirectional association between BMI and indole-3-acetic.

In humans, indole-3-acetic acid is a tryptophan metabolite that are largely generated by the direct or indirect metabolism of the gut microbiota38,39. Approximately 4–6% of tryptophan undergoes bacterial degradation to yield indole metabolites40. Since human de novo production of indole metabolites is unlikely40, the levels of indole-3-acetic acid is either a reflection of dietary intake (in this case, tryptophan-containing foods and cruciferous vegetables) that are modulated by the gut bacteria or entirely a reflection of changes in gut microbial metabolism. There is a correlation between vegetable intake and calorie intake41, therefore controlling for calorie intake and protein intake, and their interaction with BMI trajectory group minimizes the influence of differential consumption of cruciferous vegetables and tryptophan-containing foods on our findings. The fact that tryptophan only minimally attenuate BMI trajectory group differences in indole-3-acetic acid also suggests that this association is independent of this precursor.

Clostridium bartlettii, several Bacteroides species and other bacteria have been reported to produce indole-3-acetic acid42. This suggests that in individuals with long-term overweight, dysbiosis and/or altered metabolic functions of the gut microbiota results in decreased synthesis or increased utilization of indole-3-acetic acid. Although the potential of the gut bacteria of healthy humans to produce indole is very heterogeneous;43 the absence44 and lower levels45 of indoles in serum of germ-free animals compared to their conventionally raised counterparts suggest that these bacteria will be either absent or decreased in overweight individuals. Prospectively linking long-term overweight status with the abundance and function of the gut microbiota would help identify the altered bacteria, and linking the identified bacteria to levels of indole-3-acetic acid would help identify its producer in our study population. There are other gut microbiota-controlled tryptophan pathways46. Therefore, whether and the extent to which long-term overweight affects these pathways should be evaluated in future studies. Ultimately, indole-3-acetic acid may help to further characterize young individuals with different long-term BMI phenotypes. Overall, indolic tryptophan metabolic pathway seems to be highly dysregulated by long-term overweight.

Secondly, we observed that the levels of methionine, isoleucine, tryptophan, xanthurenic acid, and indole-3-carboxaldehyde from childhood into late adolescent were inversely related to CRP levels in late adolescence–young adulthood, but the levels of 5-hydroxyindole-3-acetic acid was directly related to CRP–a well-established marker of inflammation. Interestingly, all these metabolites are independently related to CRP, indicating that their association is not confounded by their precursors. While there is some evidence that changes in amino acids occur in inflammatory states47, it is less clear if these changes are a cause or a consequence of inflammation. Only a few prospective investigations in children and adolescent have implicated amino acid metabolites in cardiometabolic risks21,24,25,26, and of these studies only one reported relations with CRP26. In agreement with our results, Kosek et al.26 found an inverse association between tryptophan and CRP. Similarly, a cross-sectional investigation, including children and adolescents, is in line with our findings of the inverse relation of methionine and tryptophan with CRP28.

To our knowledge, no previous study in childhood, adolescents, or young adults have prospectively linked methionine, isoleucine, xanthurenic acid, indole-3-carboxaldehyde, and 5-hydroxyindole-3-acetic acid to CRP. Nevertheless, cross-sectional investigations in older adults are in line with our findings. These include an inverse association of tryptophan48 and xanthurenic acid with CRP49, and a direct association between 5-hydroxyindole-3-acetic acid and CRP50. Other studies in adults that contrast our findings include lack of association of isoleucine35, lack of association of methionine and tryptophan50, and positive relation of isoleucine51,52 with CRP. Although no study have reported an association between indole-3-carboxaldehyde and CRP; exogenous administration of indole-3-carboxaldehyde decreased the production of several inflammatory cytokines53. Consistent with our findings of several amino acids being related to CRP, a review concluded that several amino acids are involved in the development of future cardiometabolic abnormalities such as IR54. Since.we adjusted for the precursors (tryptophan and serotonin) of indole-3-carboxaldehyde, xanthurenic acid, and 5-hydroxyindole-3-acetic acid, it is unlikely that their association with CRP is due levels of these precursors or intake of diets rich in them. Systemic inflammation drives amino acid metabolism46; however our longitudinal study provides a direct evidence that variation in amino acid metabolites predates systemic inflammation.

The inflammatory role of the CRP-related amino acid metabolites in the current study have been documented. Methionine, an aliphatic, sulfur-containing, essential amino acid exerts anti-inflammatory activity through the activation of endogenous antioxidant enzymes such as methionine sulfoxide reductase A, and by counteracting oxidative stress through the biosynthesis of glutathione55. Isoleucine, a branched chain amino acid exerts anti-inflammatory activity through interference with the action and/or synthesis of prostaglandins56, and inducing the expression of β-defensins via G-protein-coupling receptors and ERK/MAPK signaling pathways57. Tryptophan, an essential aromatic amino acid, plays a critical role in controlling systemic inflammatory responses through its endothelium-derived metabolite 5-methoxytryptophan58. Xanthurenic acid is one of the several metabolites in the kynurenine pathway of tryptophan metabolism59. It reduces interferon-gamma production60 and possesses powerful antioxidant properties61. Indole-3-carboxaldehyde (indole-3-aldehyde), a gut microbiota-derived indole derivative of tryptophan catabolism produced by the action of Lactobacillus-encoded tryptophanase inhibits inflammation through activation of the aryl hydrocarbon receptor in lymphoid cells62. Finally, 5-hydroxyindole-3-acetic acid is the most abundant end product of both central and peripheral enzymatic degradation of serotonin63. Although the direct biological activity of 5-hydroxyindole-3-acetic acid is yet to be documented; its excessive production by endocrine and neuroendocrine tumors63 and the large quantities of reactive oxygen species that are produced during its biosynthesis from serotonin64 might explain its association with systemic inflammation. Epidemiological studies have reported associations between proinflammatory state among adolescents and young adults and an increased risk of future cardiovascular diseases65, thus the amino acids associated with elevated CRP in the present study could be biomarkers of proinflammatory phase leading to the development cardiovascular diseases.

One major strength of this work is that it is a prospective study in apparently healthy young individuals. This prospective investigation indicates that the obtained exposure-outcome associations are reliable. Moreover, the repeated measurement of metabolites ensures that the metabolite levels of our participants are well captured, thereby providing greater confidence in our findings. In addition, for both research aims, we adjusted for protein and calorie intake since the metabolic fate of amino acids is dependent on their dietary availability. We also corrected for variations in physical activity and several early life factors. Only a few previous studies adequately controlled for these covariates. Finally, metabolites were profiled in urine which is a non-invasive biosample. Considering that the concentrations of several urine and plasma amino acids are correlated66, urine may be a substitute for plasma in profiling amino acids, especially in large epidemiological studies.

Notwithstanding the strengths of our study, one limitation is that this study is observational, so it cannot confirm causal relationships. It would be necessary to determine whether a causal relation exists between long-term BMI trajectory groups and these metabolites, and between these metabolites and CRP, and if it exists the magnitude of their causal relations. One approach that may improve causal inference of association of these metabolites with CRP within an observational study setting is by examining whether genetically determined levels of these metabolites are related to CRP in Mendelian randomization analysis. Secondly, the homogeneous nature of our study population, in terms of geographical location and socioeconomic background, may limit generalizability of our findings. These findings should be externally validated on more geographically, socioeconomically, and ethnically diverse populations. Besides, residual and unmeasured confounders such as medications might have influenced our results. Additionally, single imputation of covariates may have underestimated the uncertainty around the effect estimates in our adjusted models. Several host factors such as protein/amino acid absorption, catabolism and uptake, and excretion as well as kidney function might also confound our results. Future studies should consider the assessment of the aforementioned host factors such as measurement of faecal levels of these metabolites in order to rule out malabsorption. Moreover, our findings speculate about the role of the gut microbiota, without measuring the faecal levels of these metabolites. Faecal as well as circulating levels of these metabolites would have strengthened our findings.

In conclusion, this prospective investigation in apparently healthy young individuals shows that independent of several factors, males who were overweight from childhood into late adolescent have decreased urinary levels of gut bacteria-derived indole-3-acetic acid, and that several urinary amino acids, including gut bacteria-derived indole-3-carboxaldehyde, negatively predict serum CRP in late adolescence–young adulthood. Although exactly the same metabolite is not related to both long-term overweight and CRP, the fact that decreasing levels of indole metabolites-indole-3-acetic acid and indole-3-carboxaldehyde are associated with long-term overweight and elevated CRP, respectively suggests that indole metabolites and their gut bacteria producers play an imperative role in overweight-related inflammation among young individuals. These current findings further underline how the host phenotype and the microbiota interact to influence health outcomes. More human prospective studies and animal studies are needed to better understand the role of altered indolic tryptophan metabolism and the gut microbiota in overweight-associated systemic inflammation.

Subjects and Methods

Study design and participants

The study sample was selected from participants of the DOrtmund Nutritional and Anthropometric Longitudinally Designed (DONALD) study, an ongoing, open cohort study conducted in Dortmund, Germany. This study collects data on diet, growth, development and metabolism of healthy children and adolescents since 1985. In the first few study years, approximately 300 participants >2 years old were also recruited. Since then, approximately 35–40 infants are newly recruited every year. The regular visits begin at 3 months of age. The participants return for three more visits in the first year, two in the second year and thereafter annually until young adulthood. Yearly examinations include 3-day weighed dietary records, anthropometric measurements, collection of 24-h urine samples, interviews on lifestyle and medical examinations. Since 2005, participants >18 y are invited for subsequent examinations with fasting blood withdrawal. Parental examinations (anthropometric measurements, lifestyle interviews) take place every four years. Due to the specific design of the DONALD study, participants from well-educated mothers are overrepresented. Further details of the DONALD study were described elsewhere67. The study was approved by the Ethics Committee of the University of Bonn (approval number 098/06) and conducted according to the guidelines of the Declaration of Helsinki.

Statement attesting to informed consent for study participation

For all examinations in the DONALD study, written consent was obtained from parent and/or legal guardian of participants during their childhood phase and written consent was also obtained from study participants themselves later on in life. A statement attesting to informed consent from a parent and/or legal guardian for study participation was provide as thus, “I consent to my child being medically examined and physically measured by qualified personnel. I am prepared to answer questions about my child regarding pregnancy and birth, development and diseases, as well as lifestyle factors and diet, and to prepare dietary protocols. I agree to answer questions about my own health status and lifestyle and to have my height and weight measured”.

Study sample

The sample for the current analyses was a subset of 354 males and 335 females DONALD study participants from whom we previously identified long-term BMI trajectory groups from age four to 1832. These individuals are singletons, full term births (36 to 42 weeks), had a birth weight greater than or equal to 2500 g, and had at least one BMI measurement in childhood (4–9.9 years), early adolescence (10–14.9 years), and late adolescence (15–18 years). Four trajectory groups (overweight, high-normal weight, mid-normal weight, and low-normal-weight), and three trajectory groups (high-normal weight, mid-normal weight, and low-normal-weight) were identified in males and females, respectively32. Of these individuals, 218 (111 males and 107 females) individuals provided 24-hour urine samples at three time-points over the course of BMI measurement, and one blood sample in late adolescence–young adulthood (between age 18 and 39 years) (Fig. 3). The current analyses were based on data from these 111 males and 107 females.

Figure 3
figure3

An overview of the study and its research aims.

Assessment of anthropometric variables, dietary intake and physical activity, early life and socio-economic characteristics

Anthropometric data for all participants were obtained by measurement that adhere to standard procedures during their annual study visit. BMI, standardized BMI z-scores, and their trajectories were determined, as previously reported32. Three-day weighed dietary records were used to collect nutritional data for three consecutive days. Using all three-day dietary data, the nutrient intake was computed using the continuously updated in-house nutrient database, LEBTAB, and the individual mean daily intake of energy and protein over the three record days was calculated. Further, physical activity was assessed using a detailed questionnaire about the duration and frequency of both organized and non-organized physical activity. Physical activity was then expressed as daily energy expenditure in metabolic equivalent task-hours. Parents were interviewed about familial and socio-economic characteristics. Information on birth anthropometrics were extracted from a standardized document (“Mutterpass”) given to all pregnant women in Germany. The BMI of the mother of the participants at study entry was also documented.

Urine sampling, preparation, and metabolic profiling of metabolites

Urine sampling

Annual 24-h urine sampling were scheduled for participants older than 3 or 4 years. The sampling conducted at home follows a standardized procedure after detailed instruction to the families. Participants were asked to void their bladders upon getting up in the morning; this urine sample is completely discarded. This sets the start of the collection and which ends with voiding the bladder in the next morning. The participants store the urine sample in preservative-free, Extran-cleaned (Extran, MA03; Merck, Darmstadt, Germany) 1 L plastic containers at less than −12 °C. The samples were transferred to the study centre where they were stored at −22 °C until analysis. Details of urine sampling have been presented elsewhere68.

Urine sample preparation and targeted metabolic profiling of metabolites

For each of the three 24-hour urine samples of the 111 males and 107 females in the current study, 25 µL aliquot and 225 µL of internal standard mix with water: acetonitrile 8:2 (v/v) were added (trypthophan-d5 at final concentration 1 ppm; tyrosine-d4, methionine-d4, serotonin-d4, kynurenic acid-d5, 5-hydroxyindole-acetic acid- d5 and dopamine d5 at 0.5 ppm), were loaded in 96 well multifilter plates (Millipore). The target metabolites were detected and quantified on a UHPLC-ESI-Triple-quadrupole-MS (Waters®), using an injection volume of 2 µL. Data processing was performed with Mass Lynx 4.1 software (Waters®). The 33 metabolites quantified were gamma-aminobutyric acid, methionine, valine, leucine, isoleucine, picolinic acid, quinolinic acid, serotonin, dopamine, tyrosine, phenylalanine, tyramine, 3-methoxy-p-tyramine, homovanillic acid, kynurenic acid, 5-hydroxyindole-3-acetic acid, tryptophan, kynurenine, xanthurenic acid, indole-3-acetamide, indole-3-acetic acid, indole-3-lactic acid, indole-3-propionic acid, indole-3-carboxaldehyde, indole-3-carboxylic acid, anthranilic acid, 3-hydroxyanthranilic acid, tryptamine, 5-methoxyindole-acetic acid, tryptophan methyl ester, 5-hydroxy-tryptophan, 3-hydroxykynurenine. The metabolites show a coefficient of variation lower than 1% and matrix effects, evaluated by the matrix match calibration approach, were minimal. Details of urine sample preparation and targeted metabolic profiling of amino acid metabolites can be found elsewhere69.

Blood sampling and measurement of cardiometabolic risk markers

In late adolescence–young adulthood, venous blood samples were drawn after an overnight fast, centrifuged within 15 min, and frozen at −80 °C. Circulating concentrations of HDL-C, FPG, CRP, IL-6, IL-18, adiponectin, chemerin, and leptin were measured. HDL-C was measured with the Advia 1650-Chemistry System analyser (Siemens Healthcare Diagnostics, Eschborn, Germany, FPG on a Roche/Hitachi Cobas c 311 analyzer (Basel, Switzerland), triglycerides and CRP with the Roche/Hitachi Cobas c311 analyser (Roche diagnostics, Mannheim, Germany), IL-6 with the Human IL-6 Quantikine HS ELISA (R&D Systems, Wiesbaden, Germany), IL-18 with the Human IL‐18 ELISA (Medical and Biological Laboratories, Nagoya, Japan), adiponectin with the Human Total Adiponectin/Acrp30 Quantikine ELISA kit (R&D Systems), chemerin with the Human Chemerin ELISA (BioVendor, Brno, Czech Republic), and leptin with Leptin Quantikine ELISA (R&D System) as previously described70,71.

Systolic (SBP) and diastolic blood pressures (DBP) were measured by the standard procedure at the study center, according to standardized procedures with an automated oscillometric device (Datascope Accutorr Plus, Mahwah, NJ, USA). For each participant, three consecutive BP measurements were taken at 3-min intervals after an initial 5-min rest and following a non-strenuous part of the examination. During the measurements, the participant’s back was supported in an upright position, with the right forearm resting on a table at heart level, and the legs uncrossed with feet on the floor. Therefore, in the present study, eleven CRM-SBP and DBP, serum triglycerides, HDL-C, FPG, CRP, IL-6, IL-18, adiponectin, chemerin, and leptin were analysed.

Statistical analyses

Participant characteristics

All statistical analyses were conducted using SAS 9.4 (SAS®, SAS Institute, Cary, NC). Sex-specific baseline characteristics of the study sample (n = 218, males = 111, females = 107) are presented as medians and corresponding 25th and 75th percentiles or as counts (percentages) where appropriate. Sex-specific differences in baseline characteristics according to sex were explored using the Mann–Whitney U test and chi square tests for continuous and categorical data, respectively.

Multivariable linear regression

The association between BMI trajectory groups and metabolites

All 32 metabolites and the KTR were normalized by calculating their rank normal scores using the Blom method. We used linear mixed models (PROC MIXED) to examine the association between BMI trajectory (categorical predictor variable) and each of the 33 (32 metabolites and KTR) dependent variables.

First, we determined the trends for each of the dependent variables over time (participants’ ages) by fitting unconditional linear and quadratic time models. We examined the convergence information and selected a better fitting model between the linear and quadratic time models as the one which minimizes the corrected Akaike’s Information Criterion. Time was expressed as a deviation from its mean in order to reduce multicollinearity between the linear and quadratic terms of the curvilinear model when the quadratic model indicated a better fit. The REPEATED statement was included in the PROC MIXED, and the individual was specified as the subject. The Kenward-Roger estimation method was used for calculating degrees of freedom. Due to the unequally spaced repeated measurements, we specified an exponential spatial covariance structure.

Then, we included the BMI trajectory group (categorical) variable as fixed effect and tested its association with each dependent variable. We obtained the overall significance (type 3 F-tests p-value) of the BMI trajectory and estimated its corresponding false discovery rate (FDR) p-value (q-value) by PROC MULTTEST. A combined p-value ≤ 0.05 and q-value ≤ 0.05 corrected with respect to the 33 dependent variables, were considered statistically significant. Thus, model 1 includes BMI trajectory, time and BMI trajectory by time interaction (for linear model), with quadratic time, and BMI trajectory by quadratic time interaction (for curvilinear model).

When the BMI trajectory group effect was significant for a dependent variable in model 1, we further examined the heterogeneity across BMI trajectory groups as the marginal mean difference (and 95% Confidence interval, CI) in the dependent variable using the LSMEANS statement. The confidence limits of the mean differences and p-value were adjusted for multiple comparisons with the simulate method. Model 1 was further adjusted for directed acyclic graph-identified minimal adjustment sets of covariates of the association between BMI trajectory and the dependent variables (model 2). These covariates were birth weight and length, maternal BMI, maternal pregnancy weight gain, breastfeeding duration, birth order, maternal education, and maternal employment, smoking in household, physical activity, daily energy intake, percentage of energy from protein, and two-way interactions of physical activity, daily energy intake, and percentage of energy from protein with BMI trajectory.

Association between metabolites and cardiometabolic risk markers

To address the second aim, that is, whether metabolites are related to the 11 CRM (SBP, DBP, triglycerides, HDL-C, FPG, CRP, IL-6, IL-18, adiponectin, chemerin, and leptin), we constructed a two-stage model. In the first stage, we modeled the normalized concentration of the 32 metabolites and KTR as a function of time using linear mixed models (PROC MIXED) with random coefficients and unstructured covariance-structure, and obtained individual-specific predicted value (best linear unbiased predictor, BLUP). In the second stage, in a multivariate multivariable linear model, the normalized CRM (dependent variables) were regressed on the BLUP estimates of the 33 independent variables (32 metabolites and KTR). We considered the CRM for which this model (model 1) showed significance at an overall F statistic p-value ≤ 0.05 and q-value ≤ 0.05. For significant model(s), metabolites were considered significant at p-value ≤ 0.05. In model 2, we adjusted for birth weight and length, maternal BMI, maternal pregnancy weight gain, breastfeeding duration, birth order, maternal education, and maternal employment, smoking in household, physical activity, daily energy intake, percentage of energy from protein, and BMI trajectory. The effect estimates and their 95% CIs represent the association between a 1-SD change in each metabolite and corresponding SD change in the CRM.

Handling of missing covariates

All covariates except birth weight and length, breastfeeding duration and birth order had missing values. The range of percentages of missing covariates were 2–30% in males and 1–18% in females. Using SAS function ‘proc mi’, we created a single imputed dataset in one burn in iterations with the fully conditional method, linear regression for continuous variables (maternal BMI, gestational weight gain), logistic regression for ordinal categorical variables (smoking household), and discriminant function for nominal categorical variables (maternal education and maternal employment). Despite the single imputation’s limitation of not achieving uncertainty of missing data, we opted for this technique over the optimal multiple imputation because of the complexity of applying multiple imputation in longitudinal datasets72, the unstable results in longitudinal mixed-model analysis after multiple imputation73, and the generally low proportions of missingness in our data.

Data availability

The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request and approval by the principal investigator.

References

  1. 1.

    Gungor, N. K. Overweight and obesity in children and adolescents. Journal of clinical research in pediatric endocrinology 6, 129–143, https://doi.org/10.4274/Jcrpe.1471 (2014).

    Article  PubMed  Google Scholar 

  2. 2.

    World Health Organization (WHO). Report of the Commission on Ending Childhood Obesity. Geneva, Switzerland: Ending Childhood Obesity Commission. (2016).

  3. 3.

    Chung, S. T., Onuzuruike, A. U. & Magge, S. N. Cardiometabolic risk in obese children. Annals of the New York Academy of Sciences 1411, 166–183, https://doi.org/10.1111/nyas.13602 (2018).

    ADS  Article  PubMed  PubMed Central  Google Scholar 

  4. 4.

    Mihalik, S. J. et al. Metabolomic profiling of fatty acid and amino acid metabolism in youth with obesity and type 2 diabetes: evidence for enhanced mitochondrial oxidation. Diabetes care 35, 605–611, https://doi.org/10.2337/dc11-1577 (2012).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  5. 5.

    Ellulu, M. S., Patimah, I., Khaza’ai, H., Rahmat, A. & Abed, Y. Obesity and inflammation: the linking mechanism and the complications. Archives of medical science: AMS 13, 851–863, https://doi.org/10.5114/aoms.2016.58928 (2017).

    CAS  Article  PubMed  Google Scholar 

  6. 6.

    Newgard, C. B. Metabolomics and Metabolic Diseases: Where Do We Stand? Cell metabolism 25, 43–56, https://doi.org/10.1016/j.cmet.2016.09.018 (2017).

    CAS  Article  PubMed  Google Scholar 

  7. 7.

    Gancheva, S., Jelenik, T., Álvarez-Hernández, E. & Roden, M. Interorgan Metabolic Crosstalk in Human Insulin Resistance. Physiological Reviews 98, 1371–1415, https://doi.org/10.1152/physrev.00015.2017 (2018).

    CAS  Article  PubMed  Google Scholar 

  8. 8.

    Santos Ferreira, D. L. et al. Association of pre-pregnancy body mass index with offspring metabolic profile: Analyses of 3 European prospective birth cohorts. PLoS Med 14, e1002376, https://doi.org/10.1371/journal.pmed.1002376 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  9. 9.

    Pitchika, A. et al. Associations of maternal type 1 diabetes with childhood adiposity and metabolic health in the offspring: a prospective cohort study. Diabetologia 61, 2319–2332, https://doi.org/10.1007/s00125-018-4688-x (2018).

    CAS  Article  PubMed  Google Scholar 

  10. 10.

    McCormack, S. E. et al. Circulating branched-chain amino acid concentrations are associated with obesity and future insulin resistance in children and adolescents. Pediatr Obes 8, 52–61, https://doi.org/10.1111/j.2047-6310.2012.00087.x (2013).

    CAS  Article  PubMed  Google Scholar 

  11. 11.

    Butte, N. F. et al. Global metabolomic profiling targeting childhood obesity in the Hispanic population. Am J Clin Nutr 102, 256–267, https://doi.org/10.3945/ajcn.115.111872 (2015).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  12. 12.

    Elshorbagy, A. K., Valdivia-Garcia, M., Refsum, H. & Butte, N. The Association of Cysteine with Obesity, Inflammatory Cytokines and Insulin Resistance in Hispanic Children and Adolescents. PLOS One 7, e44166, https://doi.org/10.1371/journal.pone.0044166 (2012).

    ADS  CAS  Article  PubMed  PubMed Central  Google Scholar 

  13. 13.

    Virtue, A. T. et al. The gut microbiota regulates white adipose tissue inflammation and obesity via a family of microRNAs. Science Translational Medicine 11, eaav1892, https://doi.org/10.1126/scitranslmed.aav1892 (2019).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  14. 14.

    Mangge, H. et al. Obesity-related dysregulation of the tryptophan-kynurenine metabolism: role of age and parameters of the metabolic syndrome. Obesity (Silver Spring, Md.) 22, 195–201, https://doi.org/10.1002/oby.20491 (2014).

    CAS  Article  Google Scholar 

  15. 15.

    Perng, W. et al. Metabolomic profiles and childhood obesity. Obesity (Silver Spring, Md.). 22, 2570–2578, https://doi.org/10.1002/oby.20901 (2014).

    CAS  Article  PubMed Central  Google Scholar 

  16. 16.

    Farook, V. S. et al. Metabolites as novel biomarkers for childhood obesity-related traits in Mexican-American children. Pediatr Obes 10, 320–327, https://doi.org/10.1111/ijpo.270 (2015).

    CAS  Article  PubMed  Google Scholar 

  17. 17.

    Popa, M., Stefanescu, A. M. & Dumitriu, L. Low level of urinary 5-hydroxyindole acetic acid (5 HIAA) in obese children having concomitantly high 3-methoxy-4-hydroxyphenyl glycol (MHPG) excretion. Endocrinologie 27, 29–34 (1989).

    CAS  PubMed  Google Scholar 

  18. 18.

    Galgani J.E., Cortés V. & Carrasco F. Carbohydrate, Fat, and Protein Metabolism in Obesity. In: Ahima, R. S. (eds) Metabolic Syndrome. Springer, Cham, 327-346, https://doi.org/10.1007/978-3-319-11251-0_21 (2016).

  19. 19.

    Adams, S. H. Emerging Perspectives on Essential Amino Acid Metabolism in Obesity and the Insulin-Resistant State. Advances in Nutrition 2, 445–456, https://doi.org/10.3945/an.111.000737 (2011).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  20. 20.

    Herman, M. A., She, P., Peroni, O. D., Lynch, C. J. & Kahn, B. B. Adipose tissue branched chain amino acid (BCAA) metabolism modulates circulating BCAA levels. The Journal of biological chemistry 285, 11348–11356, https://doi.org/10.1074/jbc.M109.075184 (2010).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  21. 21.

    Würtz, P. et al. Branched-Chain and Aromatic Amino Acids Are Predictors of Insulin Resistance in Young Adults. Diabetes care 36, 648–655, https://doi.org/10.2337/dc12-0895 (2013).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  22. 22.

    Zhao, X. et al. Using Metabolomic Profiles as Biomarkers for Insulin Resistance in Childhood Obesity: A Systematic Review. Journal of Diabetes Research 2016, 12, https://doi.org/10.1155/2016/8160545 (2016).

    CAS  Article  Google Scholar 

  23. 23.

    Perng, W., Rifas-Shiman, S. L., Hivert, M. F., Chavarro, J. E. & Oken, E. Branched Chain Amino Acids, Androgen Hormones, and Metabolic Risk Across Early Adolescence: A Prospective Study in Project Viva. Obesity (Silver Spring, Md.) 26, 916–926, https://doi.org/10.1002/oby.22164 (2018).

    CAS  Article  Google Scholar 

  24. 24.

    Newbern, D. et al. Sex differences in biomarkers associated with insulin resistance in obese adolescents: metabolomic profiling and principal components analysis. J Clin Endocrinol Metab 99, 4730–4739, https://doi.org/10.1210/jc.2014-2080 (2014).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  25. 25.

    Barat, P. et al. Inflammatory, endocrine and metabolic correlates of fatigue in obese children. Psychoneuroendocrinology 74, 158–163, https://doi.org/10.1016/j.psyneuen.2016.09.002 (2016).

    CAS  Article  PubMed  Google Scholar 

  26. 26.

    Kosek, M. N. et al. Plasma Tryptophan and the Kynurenine-Tryptophan Ratio are Associated with the Acquisition of Statural Growth Deficits and Oral Vaccine Underperformance in Populations with Environmental Enteropathy. The American journal of tropical medicine and hygiene 95, 928–937, https://doi.org/10.4269/ajtmh.16-0037 (2016).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  27. 27.

    Lee, A. et al. Prediction of future risk of insulin resistance and metabolic syndrome based on Korean boy’s metabolite profiling. Obesity research & clinical practice 9, 336–345, https://doi.org/10.1016/j.orcp.2014.10.220 (2015).

    CAS  Article  Google Scholar 

  28. 28.

    Weischendorff, S. et al. Reduced Plasma Amino Acid Levels During Allogeneic Hematopoietic Stem Cell Transplantation Are Associated with Systemic Inflammation and Treatment-Related Complications. Biology of Blood and Marrow Transplantation 25, 1432–1440, https://doi.org/10.1016/j.bbmt.2019.03.018 (2019).

    CAS  Article  PubMed  Google Scholar 

  29. 29.

    Zhang, S., Zeng, X., Ren, M., Mao, X. & Qiao, S. Novel metabolic and physiological functions of branched chain amino acids: a review. J Anim Sci Biotechnol 8, 10–10, https://doi.org/10.1186/s40104-016-0139-z (2017).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  30. 30.

    Mellor, A. L., Lemos, H. & Huang, L. Indoleamine 2,3-Dioxygenase and Tolerance: Where Are We Now? Frontiers in immunology 8, 1360–1360, https://doi.org/10.3389/fimmu.2017.01360 (2017).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  31. 31.

    Geserick, M. et al. Acceleration of BMI in Early Childhood and Risk of Sustained Obesity. New England Journal of Medicine 379, 1303–1312, https://doi.org/10.1056/NEJMoa1803527 (2018).

    Article  PubMed  Google Scholar 

  32. 32.

    Oluwagbemigun, K. et al. Developmental trajectories of body mass index from childhood into late adolescence and subsequent late adolescence-young adulthood cardiometabolic risk markers. Cardiovasc Diabetol 18, 9, https://doi.org/10.1186/s12933-019-0813-5 (2019).

    Article  PubMed  PubMed Central  Google Scholar 

  33. 33.

    Comitato, R., Saba, A., Turrini, A., Arganini, C. & Virgili, F. Sex Hormones and Macronutrient Metabolism. Critical Reviews in Food Science and Nutrition 55, 227–241, https://doi.org/10.1080/10408398.2011.651177 (2015).

    CAS  Article  PubMed  Google Scholar 

  34. 34.

    Dou, L. et al. The cardiovascular effect of the uremic solute indole-3 acetic acid. Journal of the American Society of Nephrology: JASN 26, 876–887, https://doi.org/10.1681/ASN.2013121283 (2015).

    CAS  Article  PubMed  Google Scholar 

  35. 35.

    Liu, Y. et al. Obesity-Associated Metabolic Signatures Correlate to Clinical and Inflammatory Profiles of Asthma: A Pilot Study. Allergy Asthma Immunol Res 10, 628–647, https://doi.org/10.4168/aair.2018.10.6.628 (2018).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  36. 36.

    Osadchiy, V. et al. Correlation of tryptophan metabolites with connectivity of extended central reward network in healthy subjects. PloS one 13, e0201772–e0201772, https://doi.org/10.1371/journal.pone.0201772 (2018).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  37. 37.

    Takada, A., Shimizu, F., Masuda, J. & Matsuoka, K. In Bioactive Food as Dietary Interventions for Diabetes (Second Edition) (eds Ronald Ross Watson & Victor R. Preedy) 265-276 (Academic Press, 2019).

  38. 38.

    Tryptophan metabolism (Homo sapiens), https://www.wikipathways.org/index.php/Pathway:WP465. Accessed 31-07-2019

  39. 39.

    Roager, H. M. & Licht, T. R. Microbial tryptophan catabolites in health and disease. Nature Communications 9, 3294, https://doi.org/10.1038/s41467-018-05470-4 (2018).

    ADS  CAS  Article  PubMed  PubMed Central  Google Scholar 

  40. 40.

    Keszthelyi, D., Troost, F. J. & Masclee, A. A. M. Understanding the role of tryptophan and serotonin metabolism in gastrointestinal function. Neurogastroenterology & Motility 21, 1239–1249, https://doi.org/10.1111/j.1365-2982.2009.01370.x (2009).

    CAS  Article  Google Scholar 

  41. 41.

    Chen, G.-C., Koh, W.-P., Yuan, J.-M., Qin, L.-Q. & van Dam, R. M. Green leafy and cruciferous vegetable consumption and risk of type 2 diabetes: results from the Singapore Chinese Health Study and meta-analysis. British Journal of Nutrition 119, 1057–1067, https://doi.org/10.1017/S0007114518000119 (2018).

    CAS  Article  PubMed  Google Scholar 

  42. 42.

    Russell, W. R. et al. Major phenylpropanoid-derived metabolites in the human gut can arise from microbial fermentation of protein. Molecular nutrition & food research 57, 523–535, https://doi.org/10.1002/mnfr.201200594 (2013).

    CAS  Article  Google Scholar 

  43. 43.

    Jaglin, M. et al. Indole, a Signaling Molecule Produced by the Gut Microbiota, Negatively Impacts Emotional Behaviors in Rats. Frontiers in Neuroscience 12, https://doi.org/10.3389/fnins.2018.00216 (2018).

  44. 44.

    Wikoff, W. R. et al. Metabolomics analysis reveals large effects of gut microflora on mammalian blood metabolites. Proceedings of the National Academy of Sciences of the United States of America 106, 3698–3703, https://doi.org/10.1073/pnas.0812874106 (2009).

    ADS  Article  PubMed  PubMed Central  Google Scholar 

  45. 45.

    Marcobal, A. et al. A metabolomic view of how the human gut microbiota impacts the host metabolome using humanized and gnotobiotic mice. The ISME journal 7, 1933–1943, https://doi.org/10.1038/ismej.2013.89 (2013).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  46. 46.

    Kennedy, P. J., Cryan, J. F., Dinan, T. G. & Clarke, G. Kynurenine pathway metabolism and the microbiota-gut-brain axis. Neuropharmacology 112, 399–412, https://doi.org/10.1016/j.neuropharm.2016.07.002 (2017).

    CAS  Article  PubMed  Google Scholar 

  47. 47.

    Waclawiková, B. & El Aidy, S. Role of Microbiota and Tryptophan Metabolites in the Remote Effect of Intestinal Inflammation on Brain and Depression. Pharmaceuticals (Basel) 11, 63, https://doi.org/10.3390/ph11030063 (2018).

    CAS  Article  Google Scholar 

  48. 48.

    Nikolaus, S. et al. Increased Tryptophan Metabolism Is Associated With Activity of Inflammatory Bowel Diseases. Gastroenterology 153, 1504–1516.e1502, https://doi.org/10.1053/j.gastro.2017.08.028 (2017).

    CAS  Article  PubMed  Google Scholar 

  49. 49.

    Zuo, H. et al. Plasma Biomarkers of Inflammation, the Kynurenine Pathway, and Risks of All-Cause, Cancer, and Cardiovascular Disease Mortality: The Hordaland Health Study. American journal of epidemiology 183, 249–258, https://doi.org/10.1093/aje/kwv242 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  50. 50.

    Afarideh, M. et al. Association of peripheral 5-hydroxyindole-3-acetic acid, a serotonin derivative, with metabolic syndrome and low-grade inflammation. Endocrine practice: official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 21, 711–718, https://doi.org/10.4158/ep14442.Or (2015).

    MathSciNet  Article  Google Scholar 

  51. 51.

    Yamakado, M. et al. Plasma Free Amino Acid Profiles Predict Four-Year Risk of Developing Diabetes, Metabolic Syndrome, Dyslipidemia, and Hypertension in Japanese Population. Scientific Reports 5, 11918, https://doi.org/10.1038/srep11918.

  52. 52.

    Shoaie, S. et al. Quantifying Diet-Induced Metabolic Changes of the Human Gut Microbiome. Cell Metab 22, 320–331, https://doi.org/10.1016/j.cmet.2015.07.001 (2015).

    CAS  Article  PubMed  Google Scholar 

  53. 53.

    Swimm, A. et al. Indoles derived from intestinal microbiota act via type I interferon signaling to limit graft-versus-host disease. Blood 132, 2506–2519, https://doi.org/10.1182/blood-2018-03-838193 (2018).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  54. 54.

    Morris, C. et al. The relationship between BMI and metabolomic profiles: a focus on amino acids. Proceedings of the Nutrition Society 71, 634–638, https://doi.org/10.1017/S0029665112000699 (2012).

    CAS  Article  PubMed  Google Scholar 

  55. 55.

    Martinez, Y. et al. The role of methionine on metabolism, oxidative stress, and diseases. Amino acids 49, 2091–2098, https://doi.org/10.1007/s00726-017-2494-2 (2017).

    CAS  Article  PubMed  Google Scholar 

  56. 56.

    Saxena, R. N., Pendse, V. K. & Khanna, N. K. Anti-inflammatory and analgesic properties of four amino-acids. Indian journal of physiology and pharmacology 28, 299–305 (1984).

    CAS  PubMed  Google Scholar 

  57. 57.

    Youkou, K. et al. Isoleucine, an Essential Amino Acid, Induces the Expression of Human Defensin 2 through the Activation of the G-Protein Coupled Receptor-ERK Pathway in the Intestinal Epithelia. Food Nutr Sci. 3(4), 548–555, https://doi.org/10.4236/fns.2012.34077 (2012).

    CAS  Article  Google Scholar 

  58. 58.

    Wang, Y.-F. et al. Endothelium-Derived 5-Methoxytryptophan Is a Circulating Anti-Inflammatory Molecule That Blocks Systemic Inflammation. Circulation Research 119, 222–236, https://doi.org/10.1161/CIRCRESAHA.116.308559 (2016).

    CAS  Article  PubMed  Google Scholar 

  59. 59.

    Favennec, M. et al. The kynurenine pathway is activated in human obesity and shifted toward kynurenine monooxygenase activation. Obesity (Silver Spring, Md.) 23, 2066–2074, https://doi.org/10.1002/oby.21199 (2015).

    CAS  Article  Google Scholar 

  60. 60.

    Maes, M., Mihaylova, I., Ruyter, M. D., Kubera, M. & Bosmans, E. The immune effects of TRYCATs (tryptophan catabolites along the IDO pathway): relevance for depression - and other conditions characterized by tryptophan depletion induced by inflammation. Neuro endocrinology letters 28, 826–831 (2007).

    CAS  PubMed  Google Scholar 

  61. 61.

    Reyes Ocampo, J. et al. Kynurenines with neuroactive and redox properties: relevance to aging and brain diseases. Oxid Med Cell Longev 2014, 646909–646909, https://doi.org/10.1155/2014/646909 (2014).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  62. 62.

    Descamps, H. C., Herrmann, B., Wiredu, D. & Thaiss, C. A. The path toward using microbial metabolites as therapies. EBioMedicine 44, 747–754, https://doi.org/10.1016/j.ebiom.2019.05.063 (2019).

    Article  PubMed  PubMed Central  Google Scholar 

  63. 63.

    Corcuff, J.-B., Chardon, L., Ridah, I. E. H. & Brossaud, J. Urinary sampling for 5HIAA and metanephrines determination: revisiting the recommendations. 6, R87, https://doi.org/10.1530/ec-17-0071 (2017).

  64. 64.

    Nocito, A. et al. Serotonin mediates oxidative stress and mitochondrial toxicity in a murine model of nonalcoholic steatohepatitis. Gastroenterology 133, 608–618, https://doi.org/10.1053/j.gastro.2007.05.019 (2007).

    CAS  Article  PubMed  Google Scholar 

  65. 65.

    DeBoer, M. D. O. systemic inflammation, and increased risk for cardiovascular disease and diabetes among adolescents: a need for screening tools to target interventions. Nutrition 29, 379–386, https://doi.org/10.1016/j.nut.2012.07.003 (2013).

    Article  PubMed  Google Scholar 

  66. 66.

    Polberger, S. K. T., Axelsson, I. E. & Räihä, N. C. R. Amino Acid Concentrations in Plasma and Urine in Very Low Birth Weight Infants Fed Protein-Unenriched or Human Milk Protein-Enriched Human Milk. Pediatrics 86, 909–915 (1990).

    CAS  PubMed  Google Scholar 

  67. 67.

    Buyken, A. E. et al. Die DONALD Kohorte. Ein aktueller Überblick zu 25 Jahren Forschung im Rahmen der Dortmund Nutritional and Anthropometric Longitudinally Designed Study. In: Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz 55 (6-7), S. 875–884, (2012).

  68. 68.

    Remer, T., Neubert, A. & Maser-Gluth, C. Anthropometry-based reference values for 24-h urinary creatinine excretion during growth and their use in endocrine and nutritional research. Am J Clin Nutr 75, 561–569, https://doi.org/10.1093/ajcn/75.3.561 (2002).

    CAS  Article  PubMed  Google Scholar 

  69. 69.

    Anesi, A. et al. Metabolic Profiling of Human Plasma and Urine, Targeting Tryptophan, Tyrosine and Branched Chain Amino Acid Pathways. Metabolites 9, https://doi.org/10.3390/metabo9110261 (2019).

  70. 70.

    Goletzke, J. et al. Increased intake of carbohydrates from sources with a higher glycemic index and lower consumption of whole grains during puberty are prospectively associated with higher IL-6 concentrations in younger adulthood among healthy individuals. The Journal of nutrition 144, 1586–1593, https://doi.org/10.3945/jn.114.193391 (2014).

    CAS  Article  PubMed  Google Scholar 

  71. 71.

    Diederichs, T. et al. Carbohydrates from Sources with a Higher Glycemic Index during Adolescence: Is Evening Rather than Morning Intake Relevant for Risk Markers of Type 2 Diabetes in Young Adulthood? Nutrients 9, https://doi.org/10.3390/nu9060591 (2017).

  72. 72.

    Huque, M. H., Carlin, J. B., Simpson, J. A. & Lee, K. J. A comparison of multiple imputation methods for missing data in longitudinal studies. BMC Medical Research Methodology 18, 168, https://doi.org/10.1186/s12874-018-0615-6 (2018).

    Article  PubMed  PubMed Central  Google Scholar 

  73. 73.

    Twisk, J., de Boer, M., de Vente, W. & Heymans, M. Multiple imputation of missing values was not necessary before performing a longitudinal mixed-model analysis. Journal of clinical epidemiology 66, 1022–1028, https://doi.org/10.1016/j.jclinepi.2013.03.017 (2013).

    Article  PubMed  Google Scholar 

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Acknowledgements

The authors would like to appreciate the DONALD study participants and their families for their interest, time, commitment, and provision of their data. We also acknowledge the support of the staffs at the study centre for data collection and processing of urine and blood samples. We also thank Stefan Benda for his support in formatting the figures. This study was financially supported by the project “Metabolic HEALTH through nutrition, microbiota and tryptophan bioMARKers in the frame of the EU Joint Programming Initiative “A Healthy Diet for a Healthy Life” (ERA HDHL - HEALTHMARK) and the respective national funding organizations: the Federal Ministry of Education and Research (BMBF), Germany (grant number: 01EA1705A), Science Foundation Ireland, Ireland (grant number, 16/ERA-HDHL/3362), and the Ministry of Education, University and Research (MIUR), Italy (CUP D43C17000100006). The DONALD study is supported by the Ministry of Science and Research of North Rhine Westphalia, Germany. Biomarker measurements were funded by the German Research Association. The German Diabetes Center is funded by the German Federal Ministry of Health and the Ministry of Culture and Science of the State North Rhine-Westphalia. This study was also supported in part by a grant from the BMBF to the German Center for Diabetes Research (DZD e.V.). This study was also supported by the “Diet-Body-Brain (DietBB)” Competence Cluster in Nutrition Research funded by the BMBF, FKZ: 01EA1809A. The funding sources had no influence on study design; in the collection, analysis, and interpretation of data; in the writing of the report; and in the decision to submit the paper for publication.

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K.O., U.A., and U.N. designed research. A.A., M.U., and F.M. measured the urine metabolites. M.R. and C.H. measured the blood cardiometabolic risk markers. K.O. performed the statistical analyses and wrote the manuscript. M.S. provided support for statistical analyses. G.C. provided input on interpretation of the results. All authors discussed the results and contributed to the final manuscript.

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Correspondence to Kolade Oluwagbemigun.

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Oluwagbemigun, K., Anesi, A., Ulaszewska, M. et al. Longitudinal relationship of amino acids and indole metabolites with long-term body mass index and cardiometabolic risk markers in young individuals. Sci Rep 10, 6399 (2020). https://doi.org/10.1038/s41598-020-63313-z

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