Original Article | Open | Published:

Children who develop type 1 diabetes early in life show low levels of carnitine and amino acids at birth: does this finding shed light on the etiopathogenesis of the disease?

Nutrition & Diabetes volume 3, page e94 (2013) | Download Citation

Abstract

Background:

Children and adolescents with overt type 1 diabetes (T1D) have been found to show an altered carnitine profile. This pattern has not previously been analyzed in neonates before onset of the disease.

Materials and methods:

Fifty children who developed T1D during the first 6 years of life, born and living in the Tuscany and Umbria Regions of Italy, were identified and 200 controls were recruited into the study. All newborns were subjected to extended neonatal screening by mass spectrometry at 48–72 h of life. Four controls for each of the 50 index cases were taken randomly and blinded in the same analytical batch. The panel used for neonatal screening consists of 13 amino acids, free carnitine, 33 acyl-carnitines and 21 ratios. All Guthrie cards are analyzed within 2 days of collection.

Results:

Total and free carnitine were found to be significantly lower in neonates who later developed T1D compared with controls. Moreover, the concentrations of the acyl-carnitines – acetyl-L-carnitine (C2), proprionylcarnitine (C3), 3-hydroxyisovalerylcarnitine (C5OH), miristoylcarnitine (C4), palmitoylcarnitine (C16) and stearoylcarnitine (C18) – were also significantly low in the cases vs controls. Furthermore, total amino-acid concentrations, expressed as the algebraic sum of all amino acids tested, showed a trend toward lower levels in cases vs controls.

Conclusions:

We found that carnitine and amino-acid deficit may be evident before the clinical appearance of T1D, possibly from birth. The evaluation of these metabolites in the neonatal period of children human leukocyte antigen genetically at ‘risk’ to develop T1D, could represent an additional tool for the prediction of T1D and could also offer the possibility to design new strategies for the primary prevention of the disease from birth.

Introduction

The mechanisms involved in the triggering of autoimmune aggression against beta cells, which leads to clinically overt type 1 diabetes (T1D), are still poorly understood, but a complex interaction between genetic,1 immunologic,2 environmental3 and epigenetic4 factors has been repeatedly postulated. Several prospective studies have demonstrated that factors operating early in life, and even in utero, may have an important role in the etiopathogenesis of T1D and/or may explain why certain individuals have an increased risk of developing the disease. These factors include dietary elements, such as short breast feeding or early exposure to cow’s milk5 as well as the early introduction of gluten into the diet,6 all of which possibly interfere with carnitine and amino-acid metabolism.

A reduced pool of free carnitine has been reported in children with overt T1D.7, 8 Based on these data, we performed a case-control study aimed at investigating the metabolic profiles of carnitines and amino acids in the first days of life and their possible relationship with the future development of T1D. We indeed found that 50 neonates, who progressed to develop T1D, had significantly low levels of total carnitine, free carnitine and acyl-carnitines, compared with levels detected in 200 controls. In addition, a trend of low levels of amino acids was detected in the same neonates. Information will also be provided on the 6-year follow-up of the index cases and of the controls subsequently enrolled in the study.

The data we have produced indicate that the carnitine and amino-acid deficit may impede the ‘negative selection’ of potentially autoreactive T cells, a process which occurs in the first days of life in the medulla of the thymus and leads to the death of the T cells by apoptosis. As a result, the autoreactive T cells escape death by apoptosis, leave the thymus and become ‘drifting mines’ in the peripheral lymphoid organs, ready, if activated, to attack and ultimately kill beta cells in the pancreatic islets. In view of our data, strategies could be designed for the primary prevention of T1D.

Materials and methods

Study population

We enrolled 50 children (26 female and 24 male subjects) with T1D diagnosed between November 2006 and May 2012 and/or followed at Meyer Children’s Hospital during the same period. The children were born between January 2005 and April 2010 in the Tuscany or Umbria Regions of Italy where an expanded neonatal screening was performed on dried blood spots (DBS). We excluded children with transient or permanent neonatal diabetes and children with monogenic diabetes. In addition, we excluded low weight (<1800 g) pre-term newborns, newborns on parenteral nutrition and newborns receiving an exsanguino-transfusion before the newborn screening test. Controls consisted of 200 neonates, 4 for each of the 50 index cases taken randomly and blinded in the same analytic batch and born around the same day (+/− 1 day). All experiments were conducted in compliance with the Institutional Review Board guidelines of the Meyer Children’s Hospital Ethic Committee which approved this study (protocol no. 234/2013).

Clinical assessment

T1D was diagnosed according to the American Diabetes Association (ADA) criteria:9 (1) glycated hemoglobin (HbA1c) 6.5% (in accordance with the National Glycohemoglobin Standardization Program certified and standardized to the Diabetes Control and Complication Trial assay); (2) fasting plasma glucose 126 mg dl−1 (7.0 mmol l−1). Fasting is defined as no caloric intake for at least 8 h; (3) 2-h plasma glucose 200 mg dl−1 (11.1 mmol l−1) during an oral glucose tolerance test. The test should be performed as described by the World Health Organization, using a glucose load containing the equivalent of 75 g anhydrous glucose dissolved in water; (4) In patients with classic symptoms of hyperglycemia or hyperglycemic crisis, a random plasma glucose 200 mg dl−1 (11.1 mmol l−1).

Islet-related-antibodies (I-r-Abs) determination

At diagnosis, 44 diabetic children were tested for the presence of islet-related-antibodies (I-r-Abs), in particular, ICA (islet cell antibodies; ICA 5 or >JDFU detected by indirect immune-fluorescence), IAA (insulin autoantibodies; IAA >1.5, radioimmunoassay method), GADA (glutamic acid decarboxylase antibodies; GADA >0.75, radioimmunoassay method); insulinoma-associated antigen-2 antibodies (IA-2A >0.75 up to 31 December 2011; IA-2A >5 from 01 January 2012, radioimmunoassay method).

HLA typing

At diagnosis, 29 diabetic children were human leukocyte antigen (HLA) typed using PCR-SSP (polymerase chain reaction-specific sequence primers; Kit-BAG, Germany).10

Metabolite profiling

The Expanded Newborn Screening Pilot Programme using liquid chromatography–tandem mass spectrometry (LC-MS/MS) has been operating in three provinces of Tuscany since January 2002. Officially mandated by legislative action, the programme has screened all babies born in Tuscany since November 2004 (35 000 per year) and all babies born in Umbria since 2010 (7500 per year) for selected acyl-carnitines and amino acids.11, 12, 13

Materials: Labeled internal standards of acyl-carnitines and amino acids were purchased from Cambridge Isotope Laboratories (Andover, MA, USA); a stock solution was made in methanol. The standard concentrations were in the range of 500–2500 μmol l−1 for amino acids, and in the range of 7.6–152 μmol l−1 for acyl-carnitines. Daily working solutions were made by dilution of the stock solution (1:200) using methanol–water 90:10 v/v. External standard blood spots for acyl-carnitines and amino acids from CDC (Atlanta, GA, USA) were run every day for each instrument. Routine MS/MS analysis is performed on two instruments (API 4000 AB SCIEX, Toronto, Canada) and one additional instrument (API 2000 AB SCIEX) for back up. The analyte concentrations are calculated automatically using the Chemoview software (API 4000 AB SCIEX). The analyte panel used for neonatal screening consists of 13 amino acids, free carnitine, 33 acyl-carnitines and 21 ratios. Guthrie card collection procedure DBS samples are routinely collected from all neonates born in the Tuscany and Umbria Regions (about 42 000 per year), as reported by la Marca and colleagues.13 Briefly blood collection (eight DBS on a Guthrie card) is recommended between 48 and 72 h after delivery. Blood samples are obtained by heel stick, spotted on filter paper (903, Whatman GmbH, Dasel, Germany), dried and sent daily by courier to the central newborn screening laboratory. An expanded newborn screening is routinely performed and includes hypothyroidism, cystic fibrosis, biotinidase deficiency and over 40 inborn errors of metabolism of amino acids, organic acids and fatty acids. A pilot project for ADA SCID started in 2011 for the entire neonatal population.14 All Guthrie cards are analyzed within 2 days of collection; after use, all cards are stored and, if not used, discarded after 10 years.

Tandem mass spectrometry. An AB SCIEX API 4000 bench-top Triple-Quad Mass Spectrometer equipped with the TurboIonSpray source was used for this study. The TurboIonSpray source operated under positive ion mode at a voltage of 5500 volts and with a ‘turbo’ gas flow of 10 l min−1 of air heated to 450 °C (nominal heating-gun temperature). Mass calibration and resolution adjustments on the resolving quadrupoles were performed automatically using a PPG 2 × 10-6 mol l−1 solution introduced via the built-in Infusion Pump. The resolution was set on both resolving quadrupoles at 0.7 amu (measured at 1/2 height) for all MS and MS/MS experiments.

Collision-activated dissociation MS/MS was performed through the LINAC Q2 collision cell, operating with 10 mTor pressure of nitrogen as collision gas. Declustering potential, collision exit potential and collision energy were automatically optimized for both unlabeled amino acids and acyl-carnitines by the ‘quantitation optimization’ option. The resulting declustering potential was +50 V, optimal collision energy and collision exit potential were seen at 26 V and 20 V, respectively.

Statistical analysis

Data were preliminarily tested for normality with K–Smirnov test, and descriptive data were accordingly expressed as mean±s.d., or median with interquartile range. Comparisons between means were performed with Student’s t-test and comparisons between medians with the Mann–Whitney test. SPSS software (13.0) was used and a P<0.05 considered statistically significant.

Results

Clinical characteristics of the children with T1D

The 50 children enrolled in the study showed classical signs and symptoms of T1D such as polyuria, polydipsia, polyphagia, enuresis, fatigue, weight loss and dehydration. At diagnosis of diabetes, the average age was 3 years and 1 month (range 8 months to 6 years). At T1D onset, the average blood glucose level was 574 mg dl−1 (31.8 mmol l−1; range 202–1243 mg dl−1), average HbA1c level was 10.9% (range 7.3–14%). Of the 50 diabetic children, 20% showed severe diabetic ketoacidosis, defined as blood pH lower than 7.1 and bicarbonate levels lower than 5 mmol l−1. Of the 50 index cases, 33 developed T1D between 0.8 and 3.8 years and 15 between 4.1 and 6.5 years. As for the 50 index cases, none of the 200 control neonates had T1D at the time of enrollment in the study and none developed T1D in the 6 years of follow-up.

Associated diseases in the T1D children and their relatives

Celiac disease (CD) was diagnosed in 11 children after T1D onset, whereas in one child CD preceded T1D onset. None of the index cases had autoimmune thyroid or other autoimmune diseases. Six children had first-degree relatives with T1D: four fathers, one mother and one sister. In addition, one father had Graves’ disease, one mother had CD and two children had second-degree relatives with T1D (two grandmothers) (Table 1).

Table 1: Clinical, familial, immunological, genetic and metabolic characteristic of the 50 children who developed T1D

Islet-related-antibodies

ICA, IAA, GADA and IA-2A were detected in 44 of the T1D children (at least one I-r-Abs), 2 children had no detectable I-r-Abs and in 4 cases I-r-Abs were not tested (Table 1).

HLA typing

We found HLA genetic susceptibility markers for T1D (DRB1*03/DRB1*04-DQB1*0302) in 27 of the 29 HLA-typed children (Table 1). Of the 50 children with T1D, 25 had both detectable I-r-Abs and HLA genetic susceptibility to T1D, 17 had detectable I-r-Abs, but were not typed for HLA, 2 had HLA genetic susceptibility to T1D, but did not have detectable I-r-Abs, 2 had detectable I-r-Abs, but did not have HLA genetic susceptibility to T1D and 4 were neither tested for I-r-Abs nor HLA typed (Table 1).

Levels of carnitines and amino acids at birth in neonates at ‘risk’ to develop T1D

Compared with controls, significantly low levels of total carnitine, free carnitine and acyl-carnitines were found in neonates who would develop T1D later in their childhood. The differences in the levels of carnitine between cases and controls showed high statistical significance (Figures 1a–c), whereas the 21 acyl/free carnitine ratios were only marginally significant (P=0.07) (Table 2). In addition, levels of 28 acyl-carnitines were approximately the same in index cases vs controls (data not shown), while the acyl-carnitines – acetyl-L-carnitine (ALCAR) (C2), proprionylcarnitine (C3), hydroxyisovalerylcarnitine (C5OH), miristoylcarnitine (C14), palmitoylcarnitine (C16) and stearoylcarnitine (C18) – showed significant differences between cases and controls (Table 2). Total amino acids showed a trend toward lower levels in the index cases compared with controls (P= 0.08), except alanine which showed a marginally significant difference (P= 0.05) (Table 3).

Figure 1
Figure 1

Box-plot of total carnitine (a), acyl-carnitine (b) and free carnitine (c) in newborns who developed T1D and in controls. The horizontal line across the box represents the median, and the box comprises 50% of the patients, an half lower and half higher than the median; vertical lines represent about the higher and the lower 25% of the patients (circles are the extreme values).

Table 2: Carnitine fractions in cases and controls (μmol l−1)
Table 3: Amino acids in cases and in controls (μmol l−1)

Discussion

All 50 children enrolled in the study had classical T1D onset, diagnosed according to the ADA criteria,9 and 92% of them had detectable I-r-Abs or T1D HLA susceptibility haplotypes confirming the autoimmune nature of their T1D. After diagnosis, none of the children discontinued insulin replacement therapy either during the honeymoon period or during the 6 years of follow-up. As concerns the controls, for each single profile (circulating concentrations of carnitines and amino acids) of a ‘case’ during the newborn screening test, four profiles present in the same analytic batch were reported as controls. Considering a potential bias, we can only state that, to date, no control has been reported to have developed T1D after 6 years of follow-up.

This is the first study to show that neonates with low levels of circulating carnitines and certain acyl-carnitines subsequently develop T1D (Figures 1a–c; Table 2). Although not significant, total amino acids showed a trend toward lower levels in cases vs controls (P=0.08) (Table 3). The points which reinforce the data obtained in our study are: (1) adequate number of index cases and appropriate choice of controls. The 50 neonates who subsequently developed T1D were matched with 200 controls, 4 for each of the index cases and born +/− 1 day; (2) a laboratory that since 2004 has enlarged the neonatal screening to 13 amino acids and to total carnitines, free carnitine and 33 acyl-carnitines; (3) the study was conducted in a completely blind fashion. By definition, the sole purpose of the neonatal screening until now has been to diagnose metabolic diseases in neonates, and not to predict T1D; (4) DBS are obtained within a few days of birth (48–72 h of life), so the blood extracted from them for measuring concentrations of amino acids and carnitines presents no problem of ‘decay’ of the metabolites to be measured.15 It should be mentioned that the neonatal screening does not test the blood of the mother; (5) unlike other case-control studies, which cannot include an exposure/outcome (or risk/disease) time sequence, in this study the potential cause occurs before the disease, a necessary requisite for inferring a cause–effect relationship.

The thymus and ‘central tolerance’ at birth

There were two reasons why we wanted to know the levels of carnitine and its derivatives in the blood of the neonates who develop T1D. The first reason was that it had been reported that children and adolescents with overt T1D showed low levels of free carnitine in the blood, although circulating levels of acyl-carnitines were high.7, 8 Comparable data were obtained in experimental models16, 17, 18. However, we found that, at birth, our cohort of future T1D patients had significant low levels not only of free carnitine, but also of some acyl-carnitines.

The reason for these apparent differences is that our index cases, when tested at birth, were normal glycemic and not overt T1D. The second, and perhaps most relevant reason, is that the blood for neonatal screening is taken from neonates in the first days of life, a period crucial for the establishment of immunologic ‘central tolerance’ in the thymus.19 In the first days of life, the thymic medulla is the site where ‘negative selection’ of potentially autoreactive T cells takes place,20 and it is in the thymic cortex that ‘positive selection’ of T cells occurs.21 When T cells are ‘positively selected’ they exit the thymus and travel to the periphery, where they are responsible for defense against foreign agents such as viruses and bacteria.22 In those first few days of life, the generation of T regulatory (Treg) cells in the thymus is also in full swing.23

But, how does ‘negative selection’ occur? Medullary thymic epithelial cells24 express almost all the tissue-specific autoantigens25, 26 which are then trimmed into 12–15 and 9 amino-acid peptides. The dodecapeptides occupy the grooves of the HLA class II molecules, whereas the nonapeptides occupy the grooves of the HLA class I molecules.27 The two HLA molecules combined with their respective peptides are inserted into the plasma membrane of the medullary thymic epithelial cells,28 which in turn expose these auto/self-peptides to potentially autoreactive CD4 and CD8 T cells. When the T-cell receptor of these potentially autoreactive CD4 and CD8 T cells encounters the auto/self-peptide in the grooves of the two HLA molecules expressed on the plasma membrane of the medullary thymic epithelial cells, the autoreactive T cells receive the ‘kiss of death’ and more than 90% of them die by apoptosis in the first days of life.29, 30

Carnitines, amino acids and ‘central tolerance’ at birth

Carnitine (3-hydroxy-4-N-trymethylamonniobutanoate) is formed from methyl-lysine liberated from the body proteins and is an essential intracellular constituent for the transport of activated long chain fatty acids across membranes.31 Carnitine is biosynthesized in biologic cells and in tissues such as the human liver and brain in relatively high concentrations, either as free carnitine or as acyl-carnitines, including ALCAR. However, we do not yet know the degree to which systemic biomarkers match cellular pools. A significant amount of carnitine is obtained from the diet (mostly from milk products and red meat).32 Evidence exists that both the fetus and the placenta can synthesize carnitine,33 even though carnitine in the fetus is largely dependent on transplacental maternal carnitine transport rather than on endogenous synthesis.34

The next question is: how are low levels at birth of circulating carnitines linked to the etiopathogenesis of T1D? Let us first consider the role and function of ALCAR (C2 in Table 2). Pettegrew and collaborators35 pointed out that ALCAR is a potentially important biologic acetylating agent which could modify amino-acid and protein dynamics, function, turnover, structure and activity by acetylating –NH2 and –OH functional groups in amino acids such as lysine, serine, threonine and tyrosine as well as N-terminal amino acids.

Most tissue-specific autoantigens are hormones or hormone precursors, for example, insulin and thyroglobulin (Tg), or enzymes, for example, glutamic acid decarboxylase and thyroid peroxidase. Amino acids are important because they either feed the production of insulin and Tg or are the substrate for the expression of enzymes, for example, glutamic acid for glutamic acid decarboxylase and tyrosine for thyroid peroxidase. However, if at birth the levels of carnitines and amino acids are low, or poorly acetylated because of the low levels of ALCAR, their structure will not be modified and consequently their function will ultimately be impaired, tissue-specific autoantigens will not be expressed in the medullary thymic epithelial cells and consequently will not be trimmed, therefore the auto/self-peptides are not produced and ultimately the grooves of the HLA class I and II molecules will be occupied by other peptides.36 As a result of this, the T-cell receptor of potentially autoreactive T cells will not interact with the HLA-groove/auto/self-peptide complex, and thus 90% of the autoreactive T cells, that normally die in the first days of life, will survive and become ‘drifting mines’ in the peripheral lymphoid organs, ready, if activated, to kill cells that are the potential target of an autoimmune attack, such as beta cells in the pancreatic islets. However, other mechanisms, including the weakening of Treg cells,37 or defective ‘peripheral tolerance’38 cannot be ruled out and may also be involved in the activation of autoreactive CD4 and CD8 T cells. Whether low levels of carnitines protect pancreatic beta cells from apoptosis is still debatable.

Carnitines and human and experimental autoimmunity

It has been reported that Leghorn-type chicks fed after hatching with high doses of L-carnitine (1000 mg kg−1) have a significantly lower thymus weight relative to body weight.39 It remains to be shown whether the high dose of L-carnitine enhances the physiologic apoptotic process in the thymic medulla of these chicks. However, ALCAR has been shown to have an anti-apoptotic effect when incubated with several cell lines,40 but there are other reports which have indicated that, conversely, 2 acyl-carnitines, palmitoylcarnitine (C16)41 and 3-hydroxy-isovalerylcarnitine (C5OH),42 have a pro-apoptotic effect on certain cell lines. Interestingly, we have found that the levels of C5OH and C16 were significantly low at birth in our cohort of future T1D cases (Table 2). It could be argued that the low levels at birth of these acyl-carnitines certainly do not help the apoptotic process which eliminates autoreactive T cells in the thymic medulla, again in the critical first days of life when ‘negative selection’ is more active. It has been observed in humans43 and in mice44 that carnitine has immunosuppressive/immunomodulating functions. Could it be that, in addition to C5OH or C16, the other acyl-carnitines, proprionylcarnitine (C3), miristoylcarnitine (C14) and stearoylcarnitine (C18), also found at low levels at birth (Table 2), are involved in particular immunologic functions in the thymus in the first days of life?

Apart from influencing ‘negative selection’, low levels of carnitines may also have an effect on the functions of other thymic cell compartments, for example, those involved in the ‘positive selection’ process,16 the generation of Treg cells23 or the functions of the thymic nurse cells, sets of cells which reside in the thymic cortex.45, 46 Obese strain chickens, which develop spontaneous autoimmune thyroiditis, are deficient in thymic nurse cells, the thymus containing only half the number of thymic nurse cells found in the thymus of normal white Leghorn chickens, beginning as early as at 17 days of embryogenesis.47 Would a high dose of carnitine, as given to Leghorn-type chicks at hatching, but given this time to obese brooding hens or to their chicks after hatching, restore the number and functions of thymic nurse cells?

What about non-obese diabetic (NOD) mice, the classic animal model of T1D? Although it has been debated whether ‘negative selection’ in NOD mice is impaired,48, 49 it would be interesting to measure amino-acid and carnitine levels in newborn NOD mice to see if female NOD mice, which have a higher prevalence of T1D compared with male NOD mice, have lower levels of carnitines and amino acids at birth. If this is so, would giving a supplement of amino acids and carnitines to pregnant mothers or to neonatal NOD mice prevent them from developing T1D?

Other relevant questions

What determines the levels of carnitines in neonates? The answer to this question might emerge from recent data showing that children 0–3 years of age and living in particular socioeconomic situations, including crowded homes or in families with poor nutritional conditions, have a threefold greater risk of developing T1D.50 Comparing their data with ours, it is interesting to note that 33 out of 50 (66%) of our index cases developed T1D between 0.8 and 3.8 years and 15 (30%) between 4.1 and 6.5 years (Table 1). Were the children in our T1D cohort living in similar conditions?

Could certain metabolic diseases enter into the T1D equation? In answer to this question, it is known that elevated concentrations of acyl-carnitines at birth are primary markers of fatty acid metabolic disorders (Table 4).51 CU/TDD (carnitine uptake/transport deficiency disorder) or SPDC (systemic primary carnitine deficiency) are exceptions, because low free carnitine levels have been found at birth in neonates who go on to develop a metabolic disorder characterized by cardiomyopathy and hypoglycemia.52 Despite the hypoglycemic episodes at birth, the level value of carnitine in our cohort of neonates who then went on to develop T1D was 17 μml l−1. In the light of our observations, it would be of interest to know if T1D will develop later in life in patients with CU/TDD–SPDC.

Table 4: Fatty acid metabolism disordersa (°=Primary markers)

Epigenetics, the ENCODE project and T1D

Epigenetic modifications, such as DNA methylation and post-translational histone modifications are indispensable for a variety of genomic processes, including maintenance of genomic integrity and regulation of gene expressions.53 By performing a genome-wide DNA methylation analysis,54 the presence of T1D-specific methylation variable positions (T1D-MVPs) was detected in 15 T1D monozygotic twins and in 7 islet cell antibody positive school children before and after they developed T1D. This report describes the first example of a disease associated with epigenetic modifications that antedate the onset of the clinical disease. It remains to be seen whether T1D-MVPs are potential etiologic factors for causing disease or rather are biomarkers. However, the relevance of these findings will certainly be reinforced if T1D-MVPs exist at birth and, if so, will support the possibility of a stochastic or environmental factor that takes effect in utero.54

Acetylation is one of the most frequent and better understood epigenetic changes in histones, neutralizing their charge and generating an open-chromatin configuration which allows the binding of transcription factors and chromatin-remodelling complexes that influence gene transcription.4 Even if we do not have evidence at the moment of histone acetylation which can confirm risk for T1D. We have already pointed out the relevant role of ALCAR in the acetylation of amino acids and proteins thereby giving them the right structure and proper activity. ALCAR, when detected at low levels at birth, may well be a potential etiologic factor, responsible for causing the disease, rather than being just a biologic marker for T1D-prediction. More relevantly, it might turn out to be the ‘spy’ of the existence of environmental factors operating in utero, and thus responsible for low levels of carnitines at birth.

The initial results of the ENCODE project (Encyclopedia of DNA Elements) indicate that 80% of the genome contains elements linked to biochemical functions filled with enhancers (regulatory DNA elements), promoters (the sites at which DNA transcription into RNA is initiated) and numerous previously overlooked regions that encode RNA transcripts that are not translated into proteins, but that might have regulatory roles.55 These results show that many DNA variants previously correlated with certain diseases lie within or very near non-coding functional DNA elements, providing new leads for linking epigenetic variations and disease. T1D-MVPs and our own data on the at-birth low levels of carnitines, both of which involve methylation and acetylation variations, may now provide the right insights for dissecting the etiopathogenesis of T1D.

Of note, poor acetylation of amino acids and proteins at birth will be a risk factor for developing T1D and other autoimmune diseases, such as autoimmune thyroid disease56 and CD57 (CD was found primarily associated with T1D in our cohort), but it must be pointed out that the ‘risk’ applied only in HLA genetically susceptible individuals (for example, HLA DR3/DR4) and not in individuals with other HLA haplotypes.

Conclusion

In conclusion, neonates that might develop T1D later in life have reduced levels, soon after birth, of circulating free carnitine and acyl-carnitines and a trend toward low levels of amino acids. Laboratory determination of these compounds is easy to perform and is routinely applied in neonatal mass screenings. The evaluation of amino-acid concentrations and carnitines in DBS could therefore represent an additional tool for HLA genotyping (HLA DR3/DR4) to predict T1D and may also give rise to new strategies for the primary prevention of T1D as early as from birth. At this point, a clinical trial, where HLA at ‘risk’ newborns will be bottle-fed with a supplementation of these nutrients or metabolites for a few weeks after birth, could be organized to prove or disprove whether the primary prevention of T1D is feasible.

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Acknowledgements

We thank Prof. Corrado Betterle from the Endocrinology Department of the University Hospital of Padova for performing the test for islet cell antibodies (ICA), Dr Gianni Messeri from the Diagnostic Laboratory of Careggi University Hospital for performing IAA, IA-2A and GADA measurements, and Prof. Chiara Azzari from the Immunology Lab of A. Meyer Children’s Hospital for performing HLA typing. We are grateful to Andreas Diedenhofen and Vincenzo Giordano from the Sigma-Tau Foundation and Sebastian Chapela from the Departamento de Bioquimica Humana, Facultad de Medicina, Universidad de Buenos Aires, UBA, Argentina, for constructive discussion. We thank Stefano Manzoni for typing the manuscript and for the art work, and Mrs Jean Ringrose for the scientific and English editing of the manuscript.

Authors contributions

GFB was responsible for the study, concept and design. GlM, SM, ST and BP acquired the data. GlM, ST, VDC and GFB analyzed and interpreted the data. VDC was responsible for the statistics. GFB drafted the manuscript. GlM, ST and VDC critically revised the manuscript.

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Affiliations

  1. Newborn Screening, Biochemistry and Pharmacology Labs, Clinic of Pediatric Neurology, A Meyer Children’s Hospital, Florence, Italy

    • G la Marca
    •  & S Malvagia
  2. NeuroFarba Department, University of Florence, Florence, Italy

    • G la Marca
  3. Juvenile Diabetes Center, A Meyer Children’s Hospital, Florence, Italy

    • S Toni
    •  & B Piccini
  4. Unit of Epidemiology, Department of Medical Directorate, Bambino Gesù Children’s Hospital, Rome, Italy

    • V Di Ciommo
  5. The Bottazzo’s House, San Marco 3315, Venice, Italy

    • G F Bottazzo

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Competing interests

The authors declare no conflict of interest.

Corresponding author

Correspondence to G F Bottazzo.

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DOI

https://doi.org/10.1038/nutd.2013.33