Compound genetic etiology in a patient with a syndrome including diabetes, intellectual deficiency and distichiasis
Orphanet Journal of Rare Diseases volume 17, Article number: 86 (2022)
We studied a young woman with atypical diabetes associated with mild intellectual disability, lymphedema distichiasis syndrome (LDS) and polymalformative syndrome including distichiasis. We used different genetic tools to identify causative pathogenic mutations and/or copy number variations.
Although proband’s, diabetes mellitus occurred during childhood, type 1 diabetes was unlikely due to the absence of detectable autoimmunity. DNA microarray analysis first identified a de novo, heterozygous deletion at the chr16q24.2 locus. Previously, thirty-three pathogenic or likely pathogenic deletions encompassing this locus have been reported in patients presenting with intellectual deficiency, obesity and/or lymphedema but not with diabetes. Of note, the deletion encompassed two topological association domains, whose one included FOXC2 that is known to be linked with LDS. Via whole-exome sequencing, we found a heterozygous, likely pathogenic variant in WFS1 (encoding wolframin endoplasmic reticulum [ER] transmembrane glycoprotein) which was inherited from her father who also had diabetes. WFS1 is known to be involved in monogenic diabetes. We also found a likely pathogenic variant in USP9X (encoding ubiquitin specific peptidase 9 X-linked) that is involved in X-linked intellectual disability, which was inherited from her mother who had dyscalculia and dyspraxia.
Our comprehensive genetic analysis suggested that the peculiar phenotypes of our patient were possibly due to the combination of multiple genetic causes including chr16q24.2 deletion, and two likely pathogenic variants in WFS1 and USP9X.
Type 2 diabetes is a non-autoimmune, multifactorial metabolic disorder characterized by chronic hyperglycemia resulting from impaired insulin secretion and altered action of insulin . Type 2 diabetes depends on various environmental components while having a high heritability ranging from 40 to 70% . Apart from common type 2 diabetes that affects most cases with non-autoimmune diabetes, there are atypical, monogenic forms of diabetes which are usually rare and severe, with an early onset. Pathogenic mutations in more than 40 genes have now been described in patients with monogenic diabetes. They cause various conditions including neonatal diabetes, maturity-onset diabetes of the young (MODY), and diabetes-associated syndromes (e.g. Wolfram syndrome due to variants in WFS1, Wolcott–Rallison syndrome) . In Wolfram syndrome (OMIM #222300), juvenile-onset- diabetes mellitus can be isolated or associated with more complex phenotypes including optic atrophy, diabetes insipidus, and deafness. Several genes linked with monogenic diabetes are actionable (such as KCNJ11 , ABCC8 , GCK , HNF1A , HNF1B [5, 6] or HNF4A ), implying a substantial change in care for the carriers of a pathogenic variant (such as specific therapeutic management and monitoring) [4, 5]. Therefore, the genetic diagnosis of patients with a suspicion of monogenic diabetes has become crucial.
Here, we performed karyotyping, DNA microarray, and whole-exome sequencing in order to detect point mutations and/or copy number variations (CNVs) putatively causing a complex syndrome (including an atypical diabetes and polymalformative syndrome) in a young woman.
Phenome of the case report
A 17-year-old girl was referred after a pediatric follow-up for a non-autoimmune diabetes and a mild intellectual disability. She was from a non-consanguineous family and had two healthy siblings.
On the maternal side, her mother is an only child, and presented with mild dyscalculia and dyspraxia. None other members of this part of the family had an intellectual disability.
On the paternal side, her father has had type 2 diabetes since age 50. There was no history of diabetes in any of the three patient’s uncles. Her paternal grandmother presented with a late isolated cataract (from age ~ 80).
She was born at 41 weeks gestation after an uneventful pregnancy. Her birth weight was 3.620 kg (67th percentile), her size was 51 cm (67th percentile), and had a normal head circumference (85th percentile). Diabetes was diagnosed at age 7 while the young girl suffered from sudden polydipsia, polyuria, and unexplained weight loss (− 1.50 kg). At hospital admission, venous glycaemia level was 5.34 g/L, with 2 + in urinary ketone testing, glycated hemoglobin A1c (HbA1c) was very high (12.8%; Normal range: < 6.5%) and C-peptide was low (0.27 ng/mL; Normal range: 1.2–4.5 ng/mL). The venous pH, blood sodium and potassium levels were normal, with alkaline reserve at 26 mmol/L. Neither islet autoantibodies, nor anti-insulin antibodies were present. Anti-GAD, anti-IA2, anti-ZNT8 antibodies were not initially analyzed. Insulin therapy was initiated and the patient was regularly followed up. HbA1c had remained between 7.5% and 8.5% overtime without episodes of ketosis or severe hypoglycemia. At the last clinical investigation at age 24, no chronic complications of diabetes were reported. Anti-GAD, anti-ZnT8 and anti-IA2 antibodies were still negative. Pancreas imaging did not show any pancreatic atrophy.
We observed a severe gain of weight at age 8, concomitant to insulin treatment, reaching the 97th percentile of body mass index (BMI) (Fig. 1). Weight gain persisted throughout puberty. No endocrine causes of obesity were found, but low limbs swelling were regularly reported by the patient suggesting lymphedema. At age 16, the patients suddenly needed more insulin (1 UI/kg). Furthermore, metformin (1 g per day) was added to insulin injections (Fig. 1). This additional treatment led to an initial and persistent weight loss and to a 40% reduction in insulin doses. Then, we have tested the action of the incretin pathway agonists on diabetes control and insulin requirement. First, a dipeptidyl peptidase 4 (DPP4) inhibitor was added to her insulin injections, and we observed a decrease in HbA1c after 3 months (8.9 to 7.9%) and 1 kg weight loss (Fig. 1). Then, we have switched from prandial insulin to glucagon-like peptide-1 receptor agonist (GLP1-RA) (Liraglutide 1.8 mg per day) associated with basal insulin only. The patient has further lost 3.6 kg (Fig. 1).
In addition, after ruling out deafness, we assessed psychomotor retardation of the patient during her childhood. She used sentences at age 6. At age 8, the intelligence quotient (IQ) test showed a mild intellectual disability (WISC III test: total IQ 68). Moreover, at age 5, the patient was diagnosed with a bilateral distichiasis in the lower and superior eyelids, complicated with keratitis, which required surgery followed by laser and recurrent epilation. She also had dental malposition and palatine tooth requiring a surgery during her childhood. At age 8, she had diurnal enuresis. Urodynamic examinations showed that the patient also had vesicoureteral reflux with retro-urethral meatal stenosis and overactive bladder. Kidney ultrasound showed renal calyceal, hypotonia and duplex kidney. Despite anticholinergic drugs, the injection of botulinum toxin was required to manage bladder instability. After puberty, at age 13, the patient suffered from painful dysmenorrhea. Pelvic ultrasound and magnetic resonance imaging showed that the patient presented with uterine septum, which required surgery.
The karyotype was normal. Through array comparative genomic hybridization (CGH) performed in the trio (proband versus both parents), we found a de novo heterozygous deletion of 693 kb (chr16q24.2; 16: 87,152,792–87,845,741 [hg19]) in the proband. The deleted region includes six protein-coding genes (Table 1). This result was confirmed by real-time PCR. According to the Human Gene Mutation Database (HGMD), none of these genes were consistently found to be linked with monogenic forms of diabetes, obesity, kidney disorders, intellectual deficiency, lymphedema and/or distichiasis. However, other deletions encompassing chr16q24.2 have already been reported in 33 patients according to ClinGen and Decipher databases (Fig. 2 and Table 2). Among them, 25 patients presented with intellectual disability (Fig. 2 and Table 2). It is noteworthy that four patients shared intellectual disability, obesity or lymphedema as observed in our patient (Fig. 2 and Table 2). Furthermore, we observed that FOXC2 which is linked with lymphedema distichiasis syndrome (LDS) (Additional file 1: Table S1) was located 550 kb downstream to the chr16q24.2 deletion. This gene encodes a transcription factor belonging to the forkhead family. Using HiC data obtained from human fetal brain, we found that the chr16q24.2 deletion encompassed two subsequent topologically association domains (TADs) (Fig. 3). FOXC2 was located in the first TAD (Fig. 3). Therefore, we have hypothesized that the deletion might disrupt the transcriptional network of FOXC2, possibly leading to lymphedema in the carriers of chr16q24.2 deletion .
Based on the WES analyses of the trio (proband versus both parents), we did not find in the proband any de novo pathogenic or likely pathogenic variant located in the 1321 genes linked with monogenic forms of diabetes, obesity, kidney disorders, lymphedema, intellectual deficiency and/or distichiasis (Additional file 1: Table S1). However, we found one new heterozygous, likely pathogenic, missense variant in WFS1 (NM_006005.3: c.424G > C/p.V142L). The heterozygous WFS1 variants have previously been found to cause autosomal dominant diabetes . This mutation that has never been reported before and that was not listed in the Genome Aggregation Database (gnomAD; v2.1.1), was inherited from her father who presented with type 2 diabetes. Furthermore, we found a likely pathogenic missense variant in USP9X (NM_001039590.2: c.3803A > G/p.Y1268C) involved in X-linked intellectual disability , which was inherited from her mother who had academic difficulties, related to dyscalculia and dyspraxia. One of the two healthy brothers of the patient did not carry neither WFS1 p.V142L variant or USP9X p.Y1268C variant. In the proband, we did not identify any rare coding mutations in FOXC2.
We describe the case of a young female whose diabetes was difficult to associate with intellectual disability, polymalformative syndrome and lymphedema distichiasis syndrome (LDS).
On the one hand, initially, the young age of the patient, the presence of ketone bodies and the low C-peptide level at diagnosis, argued in favor of type 1 diabetes . However, the absence of acidosis and of islets antibodies at diagnosis, the absence of anti-GAD, anti-IA2 and anti-ZNT8 antibodies at age 24 [11, 12], as well as the normal size of pancreas , suggested instead an atypical non-autoimmune diabetes. Furthermore, as the introduction of metformin in addition to insulin led to weight loss and a decrease in insulin needs, we hypothesized that insulin resistance was also involved in the patient’s metabolic phenotype. More recently, the unexpected effect of Liraglutide on the discontinuation of prandial insulin has been an additional argument in favor of atypical non-autoimmune diabetes [14,15,16].
On the other hand, we performed genetic investigations in front of a polymalformative syndrome and an intellectual disability.
Through our comprehensive genetic analyses, we identified a de novo 693-kb deletion in chr16q24.2. Intellectual disability, obesity, lymphedema and distichiasis have already been described in individuals carrying a pathogenic deletion at the same locus chr16q24.2 [17,18,19]. Interestingly, FOXC2 that is a major gene linked with LDS (OMIM# 153400 ) was located close to the chr16q24.2 deletion (550 kb downstream). The specific function of FOXC2 has not yet been fully explored; however, the encoded transcription factor plays an important role in the development and maintenance of venous and lymphatic valves and of mesenchymal tissues . Considering that the activity of a transcription factor depends on its expression, we hypothesized that LDS might be the result of altered expression of FOXC2, triggered by the deletion of a long-range regulatory element in chr16q24.2 [7, 17, 22]. Indeed, a growing body of research suggests that deletions can exert a pathogenic effect through disruption of DNA structural elements such as TADs, and disruption of boundaries as a major mechanism . TAD can regulate gene expression notably by the activation of an enhancer-promoter loop . As the chr16q24.2 deletion encompassed two TADs, it might cause TAD disruption, and altered FOXC2 expression leading to LDS [7, 23]. However, further studies are needed to demonstrate this assumption.
Furthermore, we identified a novel heterozygous, likely pathogenic, missense mutation in WFS1 (p.V142L) inherited from the father with diabetes. Interestingly, we observed different presentations of diabetes in the proband and her father. Contrary to the proband, diabetes in the father was polygenic-like type 2 diabetes, as it was diagnosed in adulthood and was treated with metformin and DPP4 inhibitor without any insulin. Wolfram syndrome 1 caused by homozygous or compound heterozygous mutations in WFS1 (encoding wolframin, a 100-kDa transmembrane glycoprotein localized in the secretory granules and endoplasmic reticulum [ER]). Heterozygous mutations in WFS1 have been reported to be involved in less severe phenotypes including isolated adult-onset diabetes (OMIM #614296) . A recent study has shown that GLP1-RA could be efficient for patients with diabetes and heterozygous, pathogenic WFS1 variants . The authors proposed that GLP1-RA might improve glucose regulation due to decreased ER stress leading to conservation of β-cell function and insulin secretion . Here, we hypothesized that the likely pathogenic heterozygous variant in WFS1 might possibly explain the patient's early-onset diabetes and the efficacy of GLP1-RA on prandial insulin interruption.
In addition, we found a likely pathogenic missense variant in USP9X (p.Y1268C) which was inherited from her mother who had dyscalculia and dyspraxia during her school career. USP9X encodes an enzyme that plays a key role in human neural development and the p.Y1268C mutation has been shown to be involved in X-linked intellectual disability . Furthermore, USP9X is an X-chromosome gene that escapes X-inactivation . Female patients with de novo pathogenic mutations present with mild to moderate intellectual disability (motor and language delay), and several other clinical features (including notably urogenital abnormality, hearing impairment, cleft palate or bifid uvula) . The intellectual disability could therefore be due to the likely pathogenic missense variant in USP9X associated with the impact of the deletion.
The major limitation of our study is the fact that we did not analyze the functional effect of the deletion on FOXC2 expression, and of the two variants in WFS1 and USP9X on the activity of respective encoded proteins.
In conclusion, we suggest that the patient’s complex syndrome might be due to several genetic events including a new likely pathogenic heterozygous WFS1 variant, a likely pathogenic missense USP9X variant and a chr16q24.2 deletion possibly causing the dysregulation of FOXC2 via TADs disruption (in addition to possibly other abnormalities due to the multi-gene deletion). This study demonstrates the relevance and usefulness of comprehensive genetic analyses in cases presenting with very complex phenotypes.
We collected clinical data of a female patient from pediatric and adult diabetology medical records. Family medical data have been also collected. In accordance with French laws, patient’s and her parents’ consent were obtained.
Genomic DNA samples from the proband and her two parents were extracted from peripheral blood using the QIAamp DNA Blood Midi kit (Qiagen, Valencia, CA, USA).
Conventional cytogenetic analysis was performed on peripheral blood lymphocytes from the patient using the 550-band including GTG (G-bands after trypsin and Giemsa) and RHG (R-bands by heating using Giemsa) banding for family members.
Array CGH was performed in the proband, using Agilent 180 k oligoarrays (SurePrint G3 Human CGH Microarray 4 × 180 k). Random primer labelling and hybridization were carried out with sex-matched reference DNA according to the manufacturer's recommendations and results were analyzed using cytogenomics (v18.104.22.168) software (Agilent Technologies) using ADM2 algorithm and a three-point filter.
CNV presence was confirmed in the proband and both parents by real-time PCR using primers targeting JPH3 (that was included in the CNV). Primers for the JPH3 was designed and tested using standard procedures (forward primer 5′-CCTGTGCGTCTGATCTGCT-3′, reverse primer 5′-GTCCTGCTGCTCCTTCTGAC-3′) on a LightCycler 480 Real-Time PCR System (Roche Diagnostics, Basel, Switzerland).
Whole-exome sequencing (WES)
WES was performed in the proband and both parents. For this purpose, we used SeqCap EZ MedExome + Probes (Roche) or Human Core Exome Kit (Twist Bioscience), for Illumina sequencing (on the NovaSeq6000 system). Alignment of sequence reads to the human genome (GRCh38/hg38), variant calling and variant annotation were done as previously described . For the proband and both parents, more than 98% of the target was covered with more than eight reads. Based on the clinical data of the patient (Fig. 1), we analyzed 1321 genes linked with monogenic diabetes, monogenic obesity, monogenic kidney disorders, lymphedema and/or intellectual deficiency (Additional file 1: Table S1). To assess the pathogenicity of the variants we used the standards and guidelines of the American College of Medical Genetics and Genomics (ACMG) . For the moderate pathogenic criterion PM2 and the supporting pathogenic criterion PP2, we used gnomAD browser (v2.1.1). For the supporting pathogenic criterion PP3, we used PolyPhen-2 (HumDiv), and Mutation Taster [29, 30]. The variants were written according to the nomenclature of the Human Genome Variation Society (HGVS).
To integrate recent high-throughput technologies based on chromatin interaction data at the chr16q24.2 locus, we used the 3D Genome Browser (http://3dgenome.org), provided by the Bioinformatics and Genomics Program, Pennsylvania State University . TADs were predicted from Hi-C analysis in Human fetal brain GZ .
Availability of data and materials
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The authors would like to thank the patient and her family for their cooperation. We are specifically thankful to Genetic laboratory, American Hospital, University hospital Robert Debre (Reims, France) for their cooperation and genetic investigation. We are also thankful to Hematology laboratory (University hospital, Reims France) and Pediatric diabetology Department, American Hospital (University hospital, Reims, France) for his participation.
The next-generation sequencing work was supported by grants from the French National Research Agency (ANR-10-LABX-46 [European Genomics Institute for Diabetes] and ANR-10-EQPX-07-01 [LIGAN-PM]), and from the National Center for Precision Diabetic Medicine—PreciDIAB, which is jointly supported by the French National Agency for Research (ANR-18-IBHU-0001), by the European Union (FEDER), by the Hauts-de-France Regional Council and by the European Metropolis of Lille (MEL). A.Bo is supported by the European Research Council (ERC Reg-Seq—715575).
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Le Collen, L., Delemer, B., Spodenkiewicz, M. et al. Compound genetic etiology in a patient with a syndrome including diabetes, intellectual deficiency and distichiasis. Orphanet J Rare Dis 17, 86 (2022). https://doi.org/10.1186/s13023-022-02248-2
- Childhood onset diabetes
- Genotype–phenotype relations
- Genetic disorders
- Genetic analysis
- Intellectual disability
- Wolfram syndrome