- Research article
- Open Access
Relevance of polymorphisms in MC4R and BDNF in short normal stature
BMC Pediatrics volume 18, Article number: 278 (2018)
Variation in genes of the leptinergic-melanocortinergic system influence both body weight and height. Because short normal stature (SNS) is characterized by reduced body height, delayed maturation and leanness, allelic variation of genes in this pathway are hypothesized to affect this common condition.
We analyzed the coding regions of LEP, MC4R, MRAP2 and BDNF in 185 children with SNS (height < 5th percentile) to search for non-synonymous and frameshift variants. For association studies (two-sided χ2-tests) population-based data sets (ExAC, EVS and KORA) were used. Cyclic AMP accumulation, cell surface expression, central expression and MAP kinase activation were assayed in vitro to determine the functional implications of identified variants.
We detected eleven variants predicted to be protein-altering, four in MC4R, four in BDNF, and three in MRAP2. No variants were found in LEP. In vitro analysis implied reduced function for the MC4R variant p.Met215Ile. Loss-of-function is contrary to expectations based on obesity studies, and thus does not support that this variant is relevant for SNS. The minor SNP alleles at MC4R p.Val103Ile and BDNF p.Val66Met were nominally associated with SNS.
Taken together, although genes of the leptinergic-melanocortinergic system are important for normal growth, our data do not support the involvement of rare mutations in LEP, MC4R, MRAP2 or BDNF in short normal stature.
Short stature is one of the most common reasons for referral of children to pediatric endocrinology departments. In up to 80% of cases there is no identifiable cause for the phenotype . Short normal stature (SNS) is defined as a body height below the age- and sex- specific 5th percentile and by the absence of readily detectable pathogenic causes like illness, hormonal deficiency or dysmorphic syndromes .
Human height is a complex, highly heritable and polygenic trait. A large genome-wide association study (GWAS) meta-analysis identified 697 genome-wide significant variants at 423 different loci by analysis of a population-based sample of 253,288 individuals. Together these variants explain about 20% of the heritability of adult height variation . Recently a GWAS focussed on the relevance of rare and low-frequency variants on human adult height variation. Some variants with lower minor-allele frequencies revealed effects of up to 2 cm per effect allele. Together all variants explained 27.4% of the heritability of body height .
The leptinergic-melanocortinergic-pathway, which includes leptin (LEP), the melanocortin 4 receptor (MC4R), melanocortin receptor accessory protein 2 (MRAP2) and brain derived neurotrophic factor (BDNF), is involved in the regulation of both body height [3, 5,6,7,8,9] and weight [6, 10]. Loss-of-function mutations affecting of the components of this system lead to obese phenotypes with increased linear growth [6, 8, 9].
The function of each of these genes provides evidence that they may be candidates for playing a causal role in SNS. (1) Rare homozygous loss-of-function mutations in the LEP gene  are associated with hypogonadism, frequent infections and severe early onset obesity [11, 12]. A rare non-synonymous mutation located in a highly conserved LEP position was detected in a boy with short stature and his mother. Both heterozygous carriers shared a similar phenotype of reduced appetite, pubertal delay and leanness . (2) Up to now more than 160 non-synonymous, nonsense or frameshift mutations in MC4R resulting in reduced receptor function have been described. Carriers of these mutations are mostly (extremely) obese, hyperphagic, hyperinsulinemic and display increased linear growth [5, 6, 14]. The minor alleles at two MC4R polymorphisms (rs2229616 [p.Val103Ile] and rs52820871 [p.Ile251Leu]) are associated with slightly reduced body weight [15, 16]. rs17782313, identified in GWAS of BMI/obesity  and located 3′ to MC4R, is also associated with human adult height (p = 3.80 × 10− 11) . Mc4r-deficient mice are obese with increased length , in cavefish Mc4r mutations lead to binge eating and increased body length . An artificially induced increase in MC4R activity in the early development of zebrafish embryos causes growth retardation . (3) MRAP2 influences MC4R signalling. A mutation screen in obese children and adolescents revealed that MRAP2 variants might contribute to human obesity . Additionally, we described an MRAP2 mutation leading to reduced MC4R function . Animal models demonstrate the impact of Mrap2 on metabolism, growth and development . Mice with germline deletion of Mrap2 are characterized by obesity and increased linear growth . (4) BDNF regulates, mediated by the TrkB receptor, energy homeostasis downstream of MC4R . In humans, the association of a BDNF variant was described for childhood BMI, weight and height standard deviation score (SDS) . Conditional brain-specific Bdnf knockdown resulted in increased body weight and linear growth . TrkB hypomorphic mice also showed a phenotype characterized by obesity and increased linear growth .
The phenotype comprising reduced linear growth and leanness in children with SNS  led us to hypothesize that gain-of-function variants in LEP, MC4R, MRAP2 and/or BDNF might influence this condition. Hence, we screened the coding regions of the respective genes for mutations in 185 children with SNS.
We screened 185 (120 male) unrelated children (age 12.08 ± 3.61 years, height percentile 1.60 ± 1.33, BMI 17.56 ± 2.83 kg/m2, BMI percentile 36.52 ± 26.41) with SNS. SNS was defined as height below the 5th percentile for age and sex which is not due to illness, hormonal deficiency or part of a dysmorphic syndrome. To distinguish SNS from other types of short stature, children with dysmorphic features or chronic diseases were excluded. The following laboratory parameters were measured to rule out chronic inflammation (erythrocyte sedimentation rate, blood count, C-reactive protein), celiac disease (gliadin and endomysium antibodies), hepatic disease (aspartate aminotransferase, alanine aminotransferase), or renal disease (creatinine) and hypothyroidism (free thyroxin, thyrotropin). Growth-hormone deficiency was considered to be unlikely based on insulin-like growth factor–binding protein 3 (IGFBP-3) levels and serum insulin-like growth factor I (IGF-I) [25, 26]. Probands with SNS were recruited together with their biological parents and affected siblings if available between November 2001 and March 2007 at the endocrine outpatient unit of the Children’s hospital in Gießen (Germany) [25, 26]. Growth velocity in the short stature children was normal according to routine assessement at pediatricians and measurements at up to three different time points (admission, 1st and 2nd referral).
For association studies of detected exonic SNPs with SNS, population-based data sets were used. The Exome Aggregation Consortium (ExAC) comprises exome data of 60,706 unrelated individuals sequenced as part of various genetic studies (http://exac.broadinstitute.org/, accessed on June 2nd 2015). The Exome Variant Server (EVS) is based on the NHLBI GO Exome sequencing project (ESP). We used genotype data from a total of 4300 participants from the European American population (http://evs.gs.washington.edu/EVS/accessed on June 2nd 2015). Additionally, genotype data from 7937 participants of two population based surveys from KORA (Cooperative Health Research in the Region Augsburg; ) was used. The intronic SNP rs17782313 was compared with data from the dbSNP database (http://www.ncbi.nlm.nih.gov/SNP/index.html).
Sanger re-sequencing, denaturing high performance liquid chromatography (WAVE, ) and high resolution melting (HRM, ) were used to detect variations in the coding regions of LEP, MC4R, MRAP2 and BDNF (for details see Additional file 1: Table S1).
Conservation was analyzed by aligning the sequences of 55 (MC4R) and 61 (BDNF) species in total using orthologous data from the database Ensembl (http://www.ensembl.org/index.html, accessed on April 26th 2015, see Additional file 1: Figure S1).
In vitro analyses
The rare novel MC4R variant p.Met215Ile was analysed in vitro (cAMP accumulation assay; MAP kinase activation via serum response element (SRE) luciferase reporter gene assay and cell surface expression; for details see Additional file 1: Text S1).
The amount of total BDNF mRNA (proBDNF) and the longest mRNA (pre-pro-BDNF isoform, Chr. 11: 27,654,893-27,701,053; ENST00000438929; Ensembl) in the human brain were analyzed with a human brain cDNA array (Tissue Scan Human Brain Tissue qPCR Array HBRT101, Origene, Rockville, MD, USA). To amplify specifically the longest BDNF transcript, primers were designed to include the exon-intron boundaries of BDNF exons VIII and IX (see Fig. 1). The amount of the core BDNF transcripts (including all splice forms) was analyzed by a PCR fragment within BDNF exon IX. GAPDH served as a housekeeping control gene  (for details see Additional file 1: Table S2). Expression analysis studies were performed on the Tissue Scan Human Brain Tissue qPCR Array HBRT101 (Origene, Rockville, MD, USA) comprising 24 different brain tissues. qPCR was conducted with RT2 SYBR® Green Rox™ qPCR Mastermix (Qiagen) according to the manufacturer’s instructions.
For association analysis, we used published data from epidemiological studies (see above). To test for association between identified variants and SNS, two-sided χ2-tests were used and nominal p-values are given. Correction for multiple testing was not performed. Hardy-Weinberg equilibrium was tested in the SNS study group. For cAMP accumulation and MAP kinase activation, data analysis and statistics were done using GraphPad Prism (GraphPad Software, San Diego, CA, USA). An uncorrected p-value of 0.05 was used to denote nominal significance. The statistical difference in maximal stimulation analyses was calculated by a t-test with Welsh correction.
Mutation screens of the coding regions of LEP, MC4R, MRAP2 and BDNF revealed a total of 11 variants (Table 1). We did not further analyse MRAP2, as only synonymous variants were detected, and LEP, as we did not detect variation in the coding region.
Four non-synonymous variants in MC4R were identified (Table 1). The rare non-synonymous, conservative MC4R variant p.Met215Ile was heterozygous in an 11.13-year-old male. The substitution is at a highly conserved position (98.2%; 54 out of 55 species show the human wild type amino acid at this position, Additional file 1: Figure S1). In vitro studies revealed differences between wild-type and p.215Ile MC4R (Fig. 2a). Cell surface expression was slightly but significantly reduced to 80% of wild-type expression for p.215Ile MC4R. cAMP accumulation was nominally reduced after NDP-α-MSH challenge for p.215Ile. However, EC50 values of the mutation were slightly improved (1.6 nM for wild-type MC4R and 0.7 nM for p.215Ile, Fig. 2b). Stimulation with the endogenous ligand α-MSH revealed a strong reduction of maximal signalling to 39.6% of wild-type MC4R signalling, but nearly identical EC50 values (30 nM for wild-type and 33 nM for p.215Ile) were observed (Fig. 2b). Investigation of MAP kinase signalling indicated a complete loss-of-function for p.215Ile, which did not allow proper calculation of EC50 values for the mutation. Wild-type MC4R signalling resulted in an EC50 of 4.2 nM for NDP-α-MSH and 229 nM for α-MSH (Fig. 2c). This finding indicates a much stronger effect of the mutation on MAP kinase signalling compared to Gs/adenylyl cyclase activation. The amino acid methionine at position 215 is highly conserved and is located at a hot spot for receptor function related to the activation mechanism (Fig. 3). The slight trend toward improved signaling in Gs/adenylyl cyclase activation and the complete loss of function in terms of MAPK activation of the MC4R-215Ile mutation indicates differential signaling capacities (also known as biased signaling ) of the mutant. From these in vitro data we could only speculate that the net effect of both signaling pathways of this variant results in loss of function.
The MC4R variant rs13447329 (p.Thr112Met) was heterozygous in two unrelated probands (Additional file 1: Table S4). This variant leads to a non-synonymous, non-conservative substitution at a conserved position (70.9%, Additional file 1: Figure S1). The 15-year-old male adolescent had a delayed bone age (bone age retardation: − 2.28 years), while the 17-year-old female adolescent had a reduced leptin level of 6.4 μg/L (leptin SDS: − 0.90). Her bone age was also slightly delayed (bone age retardation: − 0.27 years). Most functional in vitro analyses showed a similar function as the wild type MC4R, while some implicated a reduced function . As the variant was frequently detected among obese and normal weight and height individuals , a role in SNS is unlikely.
Two MC4R polymorphisms rs52820871 (p.Ile251Leu) and rs2229616 (p.Val103Ile) were also detected. Four children were heterozygous for the non-synonymous polymorphism p.Ile251Leu. This SNP leads to a conservative amino acid substitution and is located at a conserved position (78.2%, Additional file 1: Figure S1). The non-synonymous, conservative polymorphism rs2229616 (p.Val103Ile) was heterozygous in a total of 12 subjects. This polymorphism is located at a highly conserved position (94.5%, Additional file 1: Figure S1). For both minor alleles (251Leu and 103Ile, respectively), a slightly increased MC4R function has been described [14,15,16, 32], which is concordant with a weight-lowering effect.
For association analyses, we used published data from large-scale population-based sequencing projects as controls (Additional file 1: Table S3). We assumed that body height is normally distributed within these cohorts . For p.Ile251Leu, we detected no association (p.Ile251Leu variant carrier frequency in SNS: 2.16%, ExAC 2.00%, nominal P = 0.87; EVS 2.33%, nominal P = 0.89, Additional file 1: Table S3), but for p.Val103Ile, the variant carrier frequency in SNS (6.49%) was nominally higher compared with data from KORA (3.67%; nominal P = 0.045), EVS (3.70%; nominal P = 0.052) and ExAC (3.86%; nominal P = 0.065). The largest published meta-analyses for human adult height did not show an association for the infrequent allele at p.Val103Ile ([3, 4]). In children and adolescents, no supporting evidence from flanking markers with height could be observed among 4556 subjects . Genotyping of the GWAS-derived SNP (P = 3.8 × 10− 11) for human adult body height (rs17782313) near the MC4R gene in our 185 SNS probands (MAF = 0.25) did not confirm the association to body height (dbSNP: Hapmap CEU European MAF = 0.265 P = 0.68).
In BDNF we detected four non-synonymous variants. Variation rs8192466 (p.Thr2Ile) leads to a non-conservative, non-synonymous substitution at a highly conserved position (93.4%, Additional file 1: Figure S1). The variant was heterozygous in an 11-year-old boy with SNS (Additional file 1: Table S4). The affected child had a slight bone age retardation (− 0.57 years) and an increased leptin level of 5.02 μg/L (leptin SDS: 2.03). The boy inherited the p.2Ile variant from his mother. His 4-year-old brother carried the p.2Ile variant as well, whereas the father was a non-carrier. Additionally, all four analysed family members were heterozygous for the BDNF polymorphism rs6265 (p.Val66Met).
The conservative, non-synonymous polymorphism rs6265 (p.Val66Met) was detected in a total of 79 children with SNS (71 heterozygous; 8 homozygous). The amino acid position 66 is highly conserved (93.4%; Additional file 1: Table S1). 66Met is nominally associated with SNS (MAF = 23.51%) in comparison with ExAC (MAF = 19.26%; nominal P = 0.040) and EVS (MAF = 19.07%; nominal P = 0.034, Additional file 1: Table S3). Again, both comparisons showed a directionally consistent effect. A large meta-analysis for human height variation just failed to show nominal association for the infrequent allele at p.Val66Met with human adult height (P = 0.063; ). However, the direction of the effect is the same as above. In children with childhood obesity , p.Val66Met was also nominally associated with height (P = 0.045).
Additionally, we found two rare mutations, rs539177035 (p.Cys34PhefsTer12) and rs551669106 (p.Val56Ala) in the longest splice form of BDNF (pre-pro-BDNF isoform, BDNF-008, ENST00000438929, Ensembl). As this splice form was not well characterized, we screened a brain-derived cDNA library to analyse the central expression pattern for the splice form. BDNF was ubiquitously centrally expressed (19 of 24 different brain tissues were positive). For some regions (e.g. the medulla), BDNF-008 is the main transcript (Fig. 4). In the hypothalamus, the longest pre-pro-BDNF represented about one third of total BDNF transcripts.
We detected an infrequent frameshift mutation, rs539177035 (p.Cys34PhefsTer12), in a 10.3-year-old boy with normal Tanner stage . He had a retarded bone age (− 3 years) and a normal leptin level (1.74 μg/L; leptin SDS: − 0.21). Both his father and 7-year-old brother were heterozygous for this variant, while his mother was a non-carrier. This frameshift mutation leads to an altered reading frame from amino acid position 33. The mutated protein terminates after amino acid 44.
The conservative previously unknown non-synonymous mutation rs551669106 (p.Val56Ala) was heterozygous in a child with SNS (see Table 1). The boy inherited the mutation from his mother. Phenotype data from his mother was not available. The amino acid position 56 shows low conservation (8.2%, Additional file 1: Figure S1).
There is evidence for an involvement of the leptinergic-melanocortinergic system in body height and weight regulation. Hence, we screened the coding regions of major players in this system (LEP, MC4R, MRAP2 and BDNF) for mutations in a total of 185 unrelated children with SNS.
MC4R - relevance of p.Met215Ile and polymorphisms in short normal stature
The rare MC4R mutation p.Met215Ile was identified in addition to three previously known variants. This non-synonymous variant was detected in a lean boy with SNS. Methionine at this position is highly conserved and in relation to the activation mechanism it is located at a hot spot for receptor function (Fig. 3). In detail: Several mutations have already been reported to (selectively) influence signalling pathways transmitted by MC4R  and especially in transmembrane domain 5 (TM5) many pathogenic mutants are already known. Mutation p.Met215Ile is in close proximity e.g. to p.Met208 and p.Met218, where pathogenic mutants were also reported (Fig. 3). Interestingly, the 3-dimensional perspective on positions of pathogenic variants revealed that the known substitutions are distributed over the entire receptor and at each transmembrane helix. Hot-spots are TM2, 4, and 5. p.Met215 is not located at the direct ligand binding site close to the extracellular region and between the extracellular loops (ECLs). This implies that the mutant p.Met215Ile does not disturb the process of ligand-binding. The model rather suggests that p.Met215 is at a critical region of helix arrangements (interfaces between TM3/5/6) and is - in the inactive state conformation - tightly embedded in a hydrophobic cage constituted by amino acids from TM3 and TM6. This region is modified during the process of receptor activation, which is a prerequisite to (fully) bind G-protein or arrestin [35, 36]. It can be assumed, therefore, that any change at this position concerning side-chain volume and biochemical properties will consequently lead to restrictions in the signalling capacity. This is also reflected by the high conservation of this residue among compared sub-species (Additional file 1: Figure S1).
MC4R mutations leading to a reduced function are mainly found in (extremely) obese individuals . As linear growth in obese adolescents is increased , we hypothesized that the p.215Ile variant leads to a gain of MC4R function in a lean and small child. However, our in vitro results and in silico analyses (Fig. 4) both implied a reduced MC4R function.
Additionally, we identified three non-synonymous variants in the MC4R gene (p.Thr112Met, p.Ile251Leu and p.Val103Ile), which were previously described in both normal weight/height and obese individuals [6, 14, 37, 38]. Two of these polymorphisms (p.Ile251Leu and p.Val103Ile) protect from obesity [15, 16], which results from improved receptor function . We found nominal association of the infrequent MC4R 103Ile allele with SNS. A lookup of this variant in the largest GWAS meta-analysis for adult height (n = 253,288 ), however, did not support this association. In a GWAS for body height in children and adolescents, an association with height was not detected . We also did not find association of rs17782313, located 188 kb downstream of MC4R, in our children with SNS, although association with human height has been reported in GWAS [7, 17]. Interestingly, SNP rs5030980 in the second intron of AgRP reached genome wide significance in the recent GWAS for human body height variation  AgRP is an endogenous, inverse agonist at the MC4R. AgRP-variants could lead to an attenuated inhibition resulting in increased MC4R-function . These findings underscore the relevance of the melanocortinergic system for body height.
BDNF variants in short normal stature
The BDNF screen revealed four non-synonymous variants. A boy with SNS carried the previously detected non-conservative variant p.Thr2Ile. Additionally, his small-normal weight mother and brother also carried this mutation. This amino acid position is conserved across different species (93.4%, see Additional file 1: Figure S1). p.Thr2Ile was previously identified in a boy with idiopathic congenital central hypoventilation syndrome (CCHS). His heterozygous father showed symptoms of autonomic nervous system dysfunction but not of CCHS . Both syndromes are severe, are accompanied by gastro-oesophageal dysfunctions and can lead to reduced growth and development . However, in our SNS probands, postnatal abnormalities were not reported. Additionally, association of the p.2Ile allele with weight regulation has not yet been detected [42, 43]. The frequency of the p.2Ile allele in our SNS study group (0.54%) is comparable with other studies (0.55%; ; 0.53%; ), hence a relevance in weight regulation and SNS is unlikely.
The infrequent allele at p.Val66Met is nominally associated with SNS. A GWAMA (GWAS meta analysis) for adult height in population-based individuals  found a directionally consistent, but non-significant, trend (P = 0.063) for this allele with body height. In the Early Growth Genetics childhood obesity dataset, p.Val66Met reached nominal significance (P = 0.045) and was also directionally consistent. This polymorphism was previously described and is related to several clinical traits including obsessive-compulsive disorders , bipolar affective disorders , Parkinson disease  and eating disorders [47, 48], in some but not all studies [42, 49, 50].
p.Val66Met is expressed in the pro-domain of BDNF. In vitro studies showed a functional relevance for the minor allele . The 66Met allele affects the secretion and intracellular processing of BDNF by the activity dependent pathway and affects hippocampal function . Only little is known about the biological function of proBDNF, although recently it was shown that it facilitates hippocampal long term depression (LTD). p.Val66Met completely inhibits LTD in the hypothalamus . There are three final paths for pro-BDNF: it can (i) be modified in the Golgi and be secreted as mature BDNF, (ii) reach the synaptic space unaltered as proBDNF and be processed into mature BDNF in the synaptic space, or (iii) be secreted without digestion . A number of mechanisms affected by 66Met-BDNF can be hypothesized. First, 66Met-BDNF may alter the process of proBDNF modification with altered BDNF concentrations of immature and mature BDNF. Alternatively, this variant may lead to altered trafficking or might change receptor affinity. Chen et al. showed that 66Met-BDNF alters intracellular trafficking and proteolytic processing . Finally, 66Met-BDNF might also influence the development of other neurons. Recently, Liao and colleagues showed that BDNF plays a role in directing the projection of TrkB neurons from the arcuate nucleus in the hypothalamus to the dorsomedial hypothalamic nucleus and paraventricular hypothalamic nucleus . All these changes might affect hypothalamic functions including appetite and growth regulation.
We detected the rare frameshift variant rs539177035 (p.Cys34PhefsTer12) in a normal-weight boy with SNS. The variant was inherited from his normal-height, overweight father. The short and lean brother of the index patient also carried the variant. Additionally, we detected this variant in four of 789 analyzed fathers, three of whom transmitted this variant to their obese child. The two carrier girls were tall, while the male carrier had normal height. The deletion of two nucleotides (AT) affects BDNF exon VIII. BDNF uses four alternative translation start codons in different exons (I; VII, VIII, XI, see Fig. 1) that lead to four pre-pro BDNF isoforms . p.Cys34PhefsTer12 is located at the N-terminal pre-hormone region and results in a translational termination after amino acid 44 with the loss of the longest transcript, pre-pro-BDNF (329aa). We can assume that this mutation has a functional relevance. It was previously suggested that the length of the pre-domain might affect intracellular BDNF trafficking with a preferred secretion of the immature isoform in the presence of the longer pre-domain versions . ProBDNF and mature BDNF bind to their receptors p75 and TrkB with different affinities. While proBDNF has an important affinity to the p75 receptor, mature BDNF binds to the TrKB receptor . The absence of the longest pre-pro-BDNF might thus result in altered trafficking of proBDNF and mature BDNF. These changes might lead to altered receptor activation with an increased or prolonged activation of TrkB. We checked the height development of the heterozygous father of the SNS child who was, at ascertainment, at a normal height. We discovered, by a questionnaire, that the father had shown symptoms for constitutional delay of growth and puberty (CDGP; short stature and delayed maturity) in his youth.
Finally, we found that the rare variant p.Val56Ala also affected BDNF exon VIII. This non-synonymous variant was detected in one child with SNS. The 56Ala-BDNF variant might alter the properties of the longest pre-pro-BDNF, so that trafficking and receptor activation are altered. Hence, in summary, our results cannot exclude or definitively support a relevance of BDNF variant Val56Ala for regulation of body height.
No evidence for involvement of variants at the LEP or MRAP2 genes in SNS
We did not detect variants in the coding region of LEP. Three synonymous variants in MRAP2 were not associated with SNS. Hence, we conclude that variants in LEP and MRAP2 do not have major effects on the SNS phenotype.
Limitations of this study include: (a) the diagnosis of idiopatic short stature  was not possible for all participants, so that the minimal consensus classification SNS  was used; (b) the comparison of the population-based data with our SNS sample, in that ExAC, EVS and KORA include a wide range of ages, weights and heights. A specifically matched young control group might show stronger association for the detected variants; (c) we could not analyse the genome-wide significant variants for adult height derived from the recent large-scale GWAS [3, 4].
We analysed specific genes of major players of the leptinergic-melanocortinergic system in children and adolescents with SNS. We detected one rare MC4R mutation leading to partially reduced MC4R function, previously detected in individuals of normal height. Hence, a major relevance of this variant for SNS is unlikely. The detected MC4R polymorphism p.Val103Ile was nominally associated with SNS.
In BDNF, a novel non-synonymous variant and a rare frameshift variant, both affecting the centrally expressed longest preproBDNF transcript, were identified. Again, relevance for SNS is unlikely as persons with normal height also carry the mutation. We found association of the minor allele at the BDNF polymorphism p.Val66Met with SNS. GWAS in both children/adolescents and adults also revealed nominal associations of the minor allele with body height. In summary, our data point to an involvement of MC4R and BDNF polymorphisms with SNS, but do not support the involvement of rare mutations in LEP, MC4R, MRAP2 or BDNF in our SNS children.
Autonomic nervous system dysfunction
Brain-derived neurotrophic factor
Body mass index
Congenital central hypoventilation syndrome
Children’s Hospital of Philadelphia
half maximal effective concentration
Extracellular-signal Regulated Kinase
Exome sequencing project
Exome variant server
Exome Aggregation Consortium
Genome-wide association study
High resolution melting
Cooperative Health Research in the Region Augsburg
Long term depression
Melanocortin 4 receptor
Melanocortin 2 receptor accessory protein 2
Polymerase chain reaction
Standard deviation score
Single nucleotide polymorphism
Short normal stature
Serum response element
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We thank the participants for taking part in our study. We acknowledge support by the Open Access Publication Fund of the University of Duisburg-Essen.
The work was supported by grants from the European Union (FP7 n°45,009 NEUROFAST, n°262,055 ESGI), the Deutsche Forschungsgemeinschaft (HI1865/2–1; BI983/2–2) and the ELAN-Program funded by the Else-Kröner-Fresenius-Stiftung.
Availability of data and materials
The datasets during and/or analysed during the current study available from the corresponding author on reasonable request.
The authors have no financial relationships relevant to this article to disclose.
Ethics approval and consent to participate
Written informed consent was given by all participants and in case of minors from their parents. This study was approved by the Ethics Committees of the Universities of Duisburg-Essen (05–2954), Marburg (Studie 20/01) and Gießen (Studie 66/01), Germany. The participants were treated according to the Declaration of Helsinki.
The authors declare that they have no competing interests.
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Table S1. Primers, PCR conditions, fragment sizes and screening methods for LEP, MC4R, MRAP2 and BDNF mutation screening [59,60,61]. Table S2. PCR-fragments and primers for BDNF expression analysis. Table S3. Association analyses. Table S4: Phenotype data of the index patients and available family members with infrequent variants in BDNF and MC4R. Figure S1. Amino acid sequence conservation in MC4R and BDNF among different species (including primates, rodents, laurasiatheria, placental mammals, sauropsia and fish). Text S1. Functional in vitro analyses for p.Met215Ile MC4R . (DOCX 62 kb)
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Herrfurth, N., Volckmar, AL., Peters, T. et al. Relevance of polymorphisms in MC4R and BDNF in short normal stature. BMC Pediatr 18, 278 (2018). https://doi.org/10.1186/s12887-018-1245-1
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