Abstract
Background:
Animal models have shown that insulin-like growth factor I (IGF-I) may mediate protein-induced kidney growth. Our aim was to analyze the effect of IGF-I on protein-induced kidney growth in healthy infants.
Methods:
This is a secondary analysis of a randomized trial that compared growth of infants fed with a higher-protein (HP) (n = 169) vs. lower-protein (LP) (n = 182) formula (in the first year of life). Outcome measures were anthropometric parameters, kidney volume (cm3), and total and free IGF-I (ng/ml).
Results:
The highest levels of total and free IGF-I were found in the HP group. Both parameters correlated significantly with BMI z-score (r = 0.229, P < 0.001 and r = 0.223, P < 0.001, respectively), kidney volume (r = 0.115, P = 0.006 and r = 0.208, P < 0.001, respectively), and kidney volume/body length (r = 0.109, P = 0.010 and r = 0.194, P < 0.001, respectively) at 6 mo. Linear regression analyses showed a significant effect of free IGF-I on kidney volume in models, including significant effects of HP formula and anthropometry. The structural equation model revealed a significant direct effect of the HP formula on kidney volume and an indirect effect mediated by free IGF-I.
Conclusion:
This study suggests that IGF-I partly mediates protein-induced kidney growth in healthy infants. IGF-I could be involved in a pathway for the programming of the renal system.
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Main
Recent research on the early origins of adult diseases has highlighted the importance of nutrition early in life. Early nutrition could affect body structures and tissue development, which could be expressed as a permanent effect on a function that could affect health in adulthood (1). This is what is known as nutritional programming. Nutritional factors could act in different tissues and systems during a critical period of development affecting growth (2). Programming through early growth mechanisms may affect different body tissues and organs, such as bone, muscle, adipose tissue, the heart, and the kidney. Different nutritional interventions early in life have been shown to produce permanent effects on kidney function and structure. For instance, it has been proposed that poor nutritional status during gestation may affect nephrogenesis in the offspring, which could lead to impaired kidney development that could induce hypertension risk as well as poor kidney function in adulthood (3,4). Conversely, increased protein supply has been reported to stimulate kidney growth not only prenatally but also in postnatal life, both in animal models (5) and in humans (6). One of the mechanisms that may induce compensatory kidney growth in response to an increase in protein supply is the increased renal workload in response to urea and other compounds derived from protein metabolism (7,8). Furthermore, animal models have shown that insulin-like growth factor I (IGF-I) may also mediate protein-induced kidney growth. However, there is little evidence suggesting a direct effect of IGF-I on kidney size or function in humans. The relationship between IGF-I and kidney volume in humans has been postulated in different scenarios. In patients with unilateral nephrectomies, compensatory growth of the remaining kidney is accompanied by an increase in IGF-I levels (9). Human recombinant IGF-I treatment also promoted an increase in kidney size and function in a series of patients with chronic renal failure (10) and in a series of healthy patients (11).
In healthy infants, it has been demonstrated that increased protein intake stimulates kidney growth (6) and is also directly related to higher serum IGF-I concentrations (12,13). However, the possible mediation of kidney growth by IGF-I has not been tested. Deciphering this mechanism could lead to a better understanding of the possible pathways for programming kidney and cardiovascular disease, such as renal insufficiency or hypertension. The aim of this study was to analyze the effects of IGF-I on protein-induced kidney growth in healthy infants.
Results
Study Sample
Of the 652 formula-fed infants remaining in the study at 6 mo (324 higher-protein (HP) formula-fed and 328 lower-protein (LP) formula-fed), 601 (92%) returned to the study centers for the kidney ultrasound assessment. Of those, 50 (8.3%) were not included in the analyses due to measurement errors or kidney anomalies. Of the remaining 551 participants in the formula-fed groups, 46 (8.3%) declined to perform the blood sample analysis. A blood sample was drawn from 506 formula-fed infants, and 438 IGF-I measurements were valid (68 blood samples did not have enough serum or were excluded for other reasons) ( Figure 1 ). There were no differences in anthropometric and socioeconomic baseline characteristics of children randomized to the formula groups. We did not find any effect of gender, country, or feeding group in withdrawals or reasons for sample exclusion ( Figure 1 ).
Of the 236 breastfed (BF) infants remaining in the study at 6 mo, 204 had a kidney ultrasound, and 186 were analyzed for comparison as well (18 (10%) were excluded for incorrect measurements or kidney anomalies). Of those, 185 participated in the blood sample analysis. IGF-I concentrations were obtained from 165 BF infants.
Effect of Protein Intake on Body and Kidney Growth
Feeding groups exhibited significant differences in anthropometrical parameters and kidney volume at 6 mo. Infants fed with the HP formula had significantly higher body weight z-scores (P = 0.009) than did the infants fed with the LP formula ( Figure 2a ), whereas no differences existed for body length z-score (0.38 (±0.96) vs. 0.33 (0.90)). Kidney volume was also significantly greater among the infants fed with the HP formula (P < 0.001) ( Figure 2b ).
Effect of Protein Intake on Total and Free IGF-I
The highest levels of total and free IGF-I were found in the HP group, which exhibited an ~35% increase in median levels as compared with the LP group (P < 0.001 for total and free IGF-I between formula groups) ( Figure 3a , b ).
Relationship Among the IGF-I Axis, Anthropometry, and the Kidney
Total and free IGF-I were significantly correlated with all anthropometric parameters (weight, length, BMI, and body surface area) at 6 mo ( Table 1 ) among formula-fed infants.
IGF-I was also correlated with kidney volume; the correlation was slightly stronger for free IGF-I in formula-fed infants ( Table 1 ). Similarly, free IGF-I was significantly correlated with estimated glomerular filtration rate (r = 0.22, P < 0.001).
Effect of the IGF-I Axis on Protein-Induced Kidney Growth
Linear regression analyses revealed a slight effect of total IGF-I concentrations on kidney volume (β = 0.025 (0.005, 0.046), P = 0.016) in a linear regression model including the infant formula; however, this effect disappeared after adjusting for current anthropometrical variables.
Free IGF-I concentrations showed a stronger effect on kidney volume in a linear regression model including the type of formula and current anthropometrical parameters, and adjusted for country and gender, explaining up to 22.3% of its variability (P < 0.001) ( Table 2 ).
Breastfeeding showed no effect on kidney volume as compared with the lower-protein formula. The effect of gender on kidney volume disappeared after adjustment for anthropometrical variables.
The direct and indirect effects of the formula and IGF-I on kidney volume were calculated in a structural equation model. The strongest effect of the intervention on kidney volume was direct (the HP formula increased the standardized kidney volume by 0.12 (95% confidence interval 0.19, 0.45) as compared with the LP formula). In addition, the HP formula had a significant indirect effect through increasing free IGF-I, which in turn had a direct and an indirect (through weight) positive effect on kidney volume. The total of all indirect effects can be derived by adding the product results along each path (i.e., 0.16 × 0.14 (formula effect directly through free IGF-I) + 0.16 × 0.18 × 0.17 (formula effect through free IGF-I and weight) = 0.029). Thus, the indirect effects of formula on kidney volume through free IGF-I make up ~24.3% of its total effect ( Figure 4 ). The statistical power calculation a posteriori shows that the direct and indirect effects of the formula on kidney volume had a power of 100%, with a confidence interval of 95%.
Discussion
IGF-I and the Kidney
This is the first clinical trial to show that the IGF-I axis may affect kidney size and possibly kidney function in healthy infants.
Our results are consistent with those published in the literature, mainly based on animal models. Rats treated with human recombinant IGF-I exhibit kidney growth and an increase in glomerular filtration rate (14). Models for compensatory kidney growth after partial nephrectomy have shown a relationship among the operation, an increase in IGF-I levels, and subsequent compensatory kidney growth (9). The possible direct effect of the IGF-I axis on kidney growth is supported by the IGF-I receptor patterns found in both rat and human kidneys.
In our study, we found significant direct associations between the IGF-I axis and kidney volume and a slight but significant correlation between the free IGF-I axis and kidney function. It is possible that the limitations of the estimation of glomerular filtration using creatinine plasma values (through the Schwartz equation) instead of a 24-h urine evaluation could partially mask these results (7).
Animal models had previously shown a direct relation between HP intake and higher total and free IGF-I levels in the serum (15,16,17). This effect has also been shown for infants and children in observational studies (18,19,20) and, more recently, in the randomized Childhood Obesity Project (CHOP) trial (12).
A possible limitation of the study is the number of subjects available for analysis by feeding group (<50% of the infants originally recruited at birth). However, we do not expect that the effect of IGF-I on the kidney could be biased by the number of subjects available, given that we did not find differences in baseline characteristics of remaining subjects or in reasons to withdraw from the study.
IGF-I and Body Growth
The IGF-I axis has been shown to be closely related to body growth in infants (21,22) and children (22). It has been reported that IGF-I concentrations in infancy are predictive of early postnatal growth rates (22), differential length gain, and adiposity (23). In our sample, consistent with the literature, total and free IGF-I were both directly correlated with weight, length, BMI, and body surface area.
IGF-I as a Mediator of Protein-Induced Kidney Growth
Our research team has already reported a significant effect of protein intake during the first months of life on kidney size (6). Infants fed a HP diet exhibited increased levels of urea and other renal workload parameters. In turn, these metabolites were correlated with kidney volume.
Research in animal models has shown that increased renal workload (by a HP supply) could induce adaptive kidney overgrowth. In addition, HP intake stimulates IGF-I secretion, which in turn could promote kidney growth directly (17). The present work reveals that the main effect on kidney size is the one produced directly by the HP formula through yet unknown mechanisms, as shown by the mediation model analyses. Furthermore, consistent with our hypothesis, this study suggests that IGF-I may partly mediate the protein-induced kidney growth in healthy infants. IGF-I may have a direct effect on kidney growth and on body weight gain. In turn, the resultant higher body mass may cause a renal work overload through an increased production of nitrogenous products such as creatinine (7).
Therefore, a triple mechanism may induce increased kidney growth upon protein intake: compensatory kidney growth induced by the increase in nitrogen substances derived from protein metabolism (the main mechanism); hypertrophy produced by increased IGF-I secretion, which may act directly on the kidney; and protein-induced body growth (also promoted by an increase in IGF-I secretion), which may also be accompanied by kidney growth. Figure 5 shows the different pathways that may participate in protein-induced kidney growth.
However, these different pathways could have different consequences. It has been suggested that protein intake early in life may be correlated with later obesity risk (24,25,26). Published results from this randomized clinical trial show an increased weight and BMI among infants fed with the HP formula, at 2 y of life, 1 y after the end of nutritional intervention. These findings support a possible role for protein intake in nutritional programming, the proposed mechanism of which is the stimulation of the IGF-I axis. Considering that this increased body growth (programmed by IGF-I modulation early in life) could be permanent, we foresee a slight long-term effect on hyperfiltration that in turn may program kidney volume at later stages.
We hypothesize that compensatory hypertrophy through an increase in protein intake may be a reversible process that could cease with the nutritional intervention (as shown in previous work) (27). However, kidney growth accompanying body weight gain early in life and mediated by the IGF-I axis could be a permanent effect. We do not expect that this increase in kidney volume may have any health effect in healthy children during infancy, but the long-term health implications of such overgrowth, if overweight is permanently established, remain to be determined. Higher kidney volume, if promoted after birth, is not expected to cause a higher renal functional capacity (because nephrogenesis in humans finishes before the end of gestation) (28). Although the differences in kidney growth in our study sample might not be clinically relevant in the long term, on the basis of the observed results, we could hypothesize that kidney hypertrophy due to excessive body weight gain early in life could result in a permanent functional overload, with a possible increasing risk of renal disease and hypertension (29,30), resulting in kidney programming. Further follow-up of these infants may help to elucidate the possible role of IGF-I on programming the renal system, by studying the relationship among weight, kidney volume, kidney function, and hypertension later in life.
In conclusion, this randomized clinical trial suggests that the IGF-I axis affects kidney size and partly mediates protein-induced kidney growth in healthy infants. The IGF-I axis could be involved in the nutritional programming of the renal system.
Methods
Study Design
The data presented were collected in a double-blind randomized controlled trial; this is a secondary analysis of a study designed to detect differences in body growth. The details of the study have been published previously (24), in addition to other secondary analyses (12,13). Term healthy infants fed an HP formula (infant formula: 2.05 g protein/100 ml; follow-on formula: 3.2 g protein/100 ml) or an LP formula (infant formula: 1.25 g protein/100 ml; follow-on formula: 1.6 g protein/100 ml) during the first year of life were compared. The composition of HP and LP study formulas fulfilled the 1991 EU Directive on Infant and Follow-on Formulae (31) (European Commission directive 91/321), and the energy contents of the two formulas were identical. Further details of these formulas have been published elsewhere (24). Families were provided with the formulas during the first year of life and did not receive any other nutritional intervention from the study team.
In addition, as a reference for growth and development, a control group of BF infants (exclusive breastfeeding for a minimum of 3 mo) was also recruited and observed in parallel during the same period, as recommended by the European Society of Paediatric Gastroenterology, Hepatology and Nutrition (32). The results of this BF infant group are shown as a gold standard reference.
Subjects
Our target population was a sample of 652 formula-fed and 236 BF 6-mo-old infants from four European countries (Germany, Belgium, Poland, and Spain) who had been recruited during the first 8 wk of life (median age = 14 d) to participate in the EU Childhood Obesity Project. Figure 1 illustrates the recruitment, randomization, and follow-up until the age of 6 mo of studied infants.
Measurements
Anthropometry. The nude weight and the length of the infant were determined at recruitment and at 6 mo of life. BMI (weight (kg)/length (m2)) and body surface area ((m2) = ((weight (kg) × length (cm))/3,600)2) were calculated. Weight, length, and BMI were expressed as z-scores relative to the World Health Organization growth standards for BF infants (33).
Blood and urine sampling and analysis. At 6 mo of age, a venous blood sample was drawn, and a urine sample was collected using an adhesive urine collection bag. Efforts were undertaken to draw blood no less than 2 h after the last feed. Total and free IGF-I (ng/dl) were determined using a highly specific commercially available radioimmunoassay test in a single laboratory (Children’s Memorial Health Institute, Warsaw, Poland). Serum creatinine and urea (both in mg/dl), as well as urine urinary creatinine (mg/dl) and osmolarity (mmol/l), were determined at local laboratories. The estimated glomerular filtration rate (ml/(min × 1.73 m2)) was calculated according to the Schwartz equation (estimated glomerular filtration rate = (0.45 × length (cm))/(serum creatinine) (mg/dl)).
Kidney measures. Ultrasonographic kidney measurements were taken by 17 trained and blinded radiologists using a linear or sector ultrasound (5–7.5 MHz) by a posterior approach or lateral approach in the prone position to measure the longest length possible (34).
Infants who exhibited anomalous kidney development, urinary tract disease (such as hydronephrosis), or kidney asymmetry (considered as a >15% length difference between kidneys) were excluded from the analyses. Measures of length, width, maximum depth in the longitudinal section (D1), and maximum depth in the transverse section (perpendicular to the hilar region) (D2) of both kidneys were measured (cm).
Kidney volume (hereafter also “kidney size”) was calculated according to the equation for an ellipsoid (kidney volume (ml) = length × width × 0.5 (D1 + D2) × 0.523) (35) and presented as the absolute value (cm3) and corrected by body length (cm3/cm). The analysis was based on the sum of the right and left kidney volumes.
Data Analyses
Z-scores for anthropometry variables were calculated using the World Health Organization Anthro for personal computers software, version 3.2.2, 2011 (World Health Organization, Geneva, Switzerland). Descriptive results were expressed as means and SDs. Skewed variables were transformed to their logarithmic form; t-test for normally distributed variables and Mann–Whitney U-test for skewed variables were used for statistical comparisons between the feeding groups. The BF group of infants was used as a reference in descriptive analyses, but not included in analyses to relate feeding with IGF-I and kidney volume (because this was a not randomized group). Pearson’s or Spearman’s correlations were used to test for linear associations among continuous variables, as appropriate. Linear regression analysis was applied to assess the effect of feeding type (HP vs. LP formula, encoded as LP = 1 and HP = 2), total and free IGF-I, body length, and body weight on kidney volume, adjusting for the potential confounders gender (encoded as male = 1, female = 2), and country (1 = Germany, 2 = Belgium, 4 = Poland, and 5 = Spain).
Structural equation modeling (36) was performed to separate the direct and indirect effects of the type of formula and IGF-I, including the additional effects of weight, height, and study country. Structural equation modeling is a straightforward extension of multiple regression that provides estimates of the magnitude and significance of hypothesized causal connections between variables. This is performed by the decomposition of observed correlations between the analyzed variables and is best depicted in a path diagram. Because this was not the primary hypothesis of the project, we did not perform the calculation for the sample size needed a priori. Therefore, we calculated the statistical power a posteriori. The linear regression model and the structural equation model considered significant effect values in 95% confidence intervals.
Data management and statistical analyses were conducted with SAS version 9.2 (SAS Institute, Cary, NC), Stata version 12.0 (Stata, College Station, TX), and SPSS Statistics version 17.0 (SPSS, Chicago, IL).
Ethical Issues
The project was approved by the ethical committees of all study centers. Informed consent was obtained from all of the families that participated in the study.
The study followed the Declaration of Helsinki (37) and the CONSORT Statement (38).
The clinical trial was registered at http://www.clinicaltrials.gov as the EU Childhood Obesity Project (NCT00338689).
Statement of Financial Support
The studies reported herein have been conducted with partial financial support from the Commission of the European Communities, the specific RTD Programme “Quality of Life and Management of Living Resources,” within the 5th Framework Programme, research grant nos. QLRT–2001–00389 and QLK1-CT-2002-30582, and the 6th Framework Programme, contract no. 007036. This article does not necessarily reflect the views of the Commission and in no way anticipates the future policy in this area. B. K. is the recipient of a Freedom to Discover Award of the Bristol-Myers Squibb Foundation, New York, NY.
Disclosure
The authors declare no conflict of interest.
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Acknowledgements
We acknowledge the European Childhood Obesity Project group and the laboratory personnel for their hard work. We also gratefully acknowledge statistical advice from Pilar Hernández (from the Institut d’Investigació Sanitària Pere Virgili) and Joan Fernández-Ballart (from the Universitat Rovira i Virgili). European Childhood Obesity Project group: J. Beyer, M. Fritsch, G. Haile, U. Handel, I. Hannibal, S. Kreichauf, I. Pawellek, S. Schiess, S. Verwied-Jorky, R. von Kries, and M. Weber (Children’s University Hospital, University of Munich Medical Centre, Munich, Germany); M. Zaragoza-Jordana (Pediatrics Unit, Universitat Rovira i Virgili, Reus, Spain); A. Dobrzańska, R. Janas, A. Wierzbicka, A. Stolarczyk, and J. Socha (Children’s Memorial Health Institute, Warsaw, Poland); C. Carlier, E. Dain, J.N. Van Hees, J. Hoyos, F. Martin, P. Poncelet, and A. Xhonneux (ULB Bruxelles and CHC, St Vincent Liege); E. Perrin (Danone Research Centre for Specialised Nutrition, Schiphol, The Netherlands); C. Agostoni, M. Giovannini, A. Re Dionigi, E. Riva, S. Scaglioni, F. Vecchi, and E. Verducci (University of Milan).
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Luque, V., Escribano, J., Grote, V. et al. Does insulin-like growth factor-1 mediate protein-induced kidney growth in infants?: A secondary analysis from a randomized controlled trial. Pediatr Res 74, 223–229 (2013). https://doi.org/10.1038/pr.2013.87
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DOI: https://doi.org/10.1038/pr.2013.87
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