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1.
Hum Mol Genet ; 30(3-4): 265-276, 2021 04 26.
Article in English | MEDLINE | ID: mdl-33693650

ABSTRACT

Mutations in the WFS1 gene, encoding wolframin (WFS1), cause endoplasmic reticulum (ER) stress and are associated with a rare autosomal-recessive disorder known as Wolfram syndrome (WS). WS is clinically characterized by childhood-onset diabetes mellitus, optic atrophy, deafness, diabetes insipidus and neurological signs. We identified two novel WFS1 mutations in a patient with WS, namely, c.316-1G > A (in intron 3) and c.757A > T (in exon 7). Both mutations, located in the N-terminal region of the protein, were predicted to generate a truncated and inactive form of WFS1. We found that although the WFS1 protein was not expressed in peripheral blood mononuclear cells (PBMCs) of the proband, no constitutive ER stress activation could be detected in those cells. In contrast, WS proband's PBMCs produced very high levels of proinflammatory cytokines (i.e. TNF-α, IL-1ß, and IL-6) in the absence of any stimulus. WFS1 silencing in PBMCs from control subjects by means of small RNA interference also induced a pronounced proinflammatory cytokine profile. The same cytokines were also significantly higher in sera from the WS patient as compared to matched healthy controls. Moreover, the chronic inflammatory state was associated with a dominance of proinflammatory T helper 17 (Th17)-type cells over regulatory T (Treg) lymphocytes in the WS PBMCs. The identification of a state of systemic chronic inflammation associated with WFS1 deficiency may pave the way to innovative and personalized therapeutic interventions in WS.


Subject(s)
Inflammation , Leukocytes, Mononuclear/metabolism , Membrane Proteins/genetics , Mutation , Wolfram Syndrome/metabolism , Child , Cytokines/genetics , Cytokines/metabolism , Female , Gene Expression Regulation , Humans , Leukocytes, Mononuclear/immunology , Sequence Analysis, DNA , Wolfram Syndrome/genetics , Wolfram Syndrome/immunology , Wolfram Syndrome/physiopathology
2.
Article in Polish | MEDLINE | ID: mdl-21447263

ABSTRACT

INTRODUCTION: A clinical criterion of the Wolfram syndrome is the coexistence of diabetes and optic atrophy recognized before the age of 15. Diabetes present in Wolfram syndrome is a result of the selective ß cell loss and failed insulin secretion which is probably associated with non-autoimmune pathogenesis. AIM OF THE STUDY: The aim of the study was an evaluation of HLA subtypes and presence of ß-cell autoantibodies in patients with molecularly confirmed Wolfram syndrome. MATERIAL AND METHODS: 9 patients with Wolfram syndrome aged 10-24 years were examined. We also studied 218 patients with type 1 diabetes as a reference group. A control group of 176 healthy individuals was included in the study. Besides the clinical assessment the HLA typing by PCR-SSO was performed. Islet cell antibodies (ICA), antibodies to glutamic acid decarboxylase (GADA), thyrosine phosphatase antibodies (IA2A) and insulin antibodies (IAA) were also detected. RESULTS: In all nine patients the coexistence of diabetes with optic atrophy was observed and in 8/9 individuals additional symptoms were recognized. In patients with Wolfram syndrome a significantly lower age of diagnosis of diabetes (Me=5.0 years) than in type 1 diabetic children (Me=10.4; p=0.002) was observed. Studies of HLA subtypes demonstrated an increased prevalence of HLA-DQw1, DRB1⋅03 and/or 04 and DR2. A comparison of the frequency of the HLA alleles in patients with Wolfram syndrome with type 1 diabetic children showed a more frequent presence of the DRB1⋅1501 (p=0.03; OR=13.28 (2.44-72.12)) and DQB1⋅06 (p=0.016; OR=10.15 (2.49-41.35)) alleles in patients with Wolfram syndrome. CONCLUSIONS: Polish patients with Wolfram syndrome have a different profile of the HLA antigens with the presence of DR2, DQw1 and DRB3/4 allele and are negative for diabetes-related autoantibodies, which may confirm non-autoimmune ß-cell destruction in this syndrome.


Subject(s)
Autoantibodies/genetics , Diabetes Mellitus, Type 1/immunology , Genes, MHC Class II/genetics , Wolfram Syndrome/genetics , Wolfram Syndrome/immunology , Adolescent , Adult , Autoantibodies/immunology , Child , Female , HLA-DQ Antigens/genetics , HLA-DQ Antigens/immunology , HLA-DR Antigens/genetics , HLA-DR Antigens/immunology , HLA-DR2 Antigen/genetics , HLA-DR2 Antigen/immunology , HLA-DRB3 Chains , HLA-DRB4 Chains , Humans , Male , Young Adult
3.
Article in English | MEDLINE | ID: mdl-21447266

ABSTRACT

INTRODUCTION: A clinical criterion of the Wolfram syndrome is the coexistence of diabetes and optic atrophy recognized before the age of 15. Diabetes present in Wolfram syndrome is a result of the selective ß cell loss and failed insulin secretion which is probably associated with non-autoimmune pathogenesis. AIM OF THE STUDY: The aim of the study was an evaluation of HLA subtypes and presence of ß-cell autoantibodies in patients with molecularly confirmed Wolfram syndrome. MATERIAL AND METHODS: 9 patients with Wolfram syndrome aged 10-24 years were examined. We also studied 218 patients with type 1 diabetes as a reference group. A control group of 176 healthy individuals was included in the study. Besides the clinical assessment the HLA typing by PCR-SSO was performed. Islet cell antibodies (ICA), antibodies to glutamic acid decarboxylase (GADA), thyrosine phosphatase antibodies (IA2A) and insulin antibodies (IAA) were also detected. RESULTS: In all nine patients the coexistence of diabetes with optic atrophy was observed and in 8/9 individuals additional symptoms were recognized. In patients with Wolfram syndrome a significantly lower age of diagnosis of diabetes (Me=5.0 years) than in type 1 diabetic children (Me=10.4; p=0.002) was observed. Studies of HLA subtypes demonstrated an increased prevalence of HLA-DQw1, DRB1⋅03 and/or 04 and DR2. A comparison of the frequency of the HLA alleles in patients with Wolfram syndrome with type 1 diabetic children showed a more frequent presence of the DRB1⋅1501 (p=0.03; OR=13.28 (2.44-72.12)) and DQB1⋅06 (p=0.016; OR=10.15 (2.49-41.35)) alleles in patients with Wolfram syndrome. CONCLUSIONS: Polish patients with Wolfram syndrome have a different profile of the HLA antigens with the presence of DR2, DQw1 and DRB3/4 allele and are negative for diabetes-related autoantibodies, which may confirm non-autoimmune ß-cell destruction in this syndrome.


Subject(s)
Autoantibodies/immunology , Insulin-Secreting Cells/immunology , Obesity/complications , Obesity/metabolism , Wolfram Syndrome/immunology , Adolescent , Child , Female , Glucose Tolerance Test , HLA-DQ Antigens/immunology , HLA-DR Antigens/immunology , HLA-DR2 Antigen/immunology , HLA-DRB1 Chains , HLA-DRB3 Chains , Humans , Male
4.
J Pediatr Endocrinol Metab ; 17(10): 1461-4, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15526727

ABSTRACT

We report a girl with Wolfram syndrome who presented with juvenile-onset diabetes mellitus when she was 4 3/12 years old. Optic atrophy and high frequency sensorineural hearing loss were found at 7 and 9 5/12 years of age, respectively. Her younger brother also developed Wolfram syndrome when he was 3 2/12 years old. Wolfram syndrome is also called DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy and deafness). This syndrome is transmitted as an autosomal recessive trait and is a progressive neurodegenerative disorder. It should be considered in a diabetic patient with unexplained optic atrophy, hearing loss, or polyuria and polydipsia in the presence of adequate blood glucose control. Visual acuity should be checked annually in patients with juvenile-onset diabetes mellitus. Optic atrophy should be considered if visual acuity is impaired.


Subject(s)
Diabetes Mellitus, Type 1/immunology , Hearing Loss, Sensorineural/immunology , Optic Atrophy/immunology , Wolfram Syndrome/diagnosis , Adolescent , Autoantibodies/immunology , Child , Child, Preschool , Female , Glutamate Decarboxylase/immunology , Humans , Protein Tyrosine Phosphatase, Non-Receptor Type 1 , Protein Tyrosine Phosphatases/immunology , Wolfram Syndrome/immunology
6.
J Pediatr Endocrinol Metab ; 10(6): 645-51, 1997.
Article in English | MEDLINE | ID: mdl-9467137

ABSTRACT

We describe a Thai family with three children, two of whom presented with Wolfram syndrome, which is a rare syndrome characterised by diabetes insipidus, diabetes mellitus, optic atrophy, deafness and urinary tract dilatation. A girl and her younger brother had insulin-dependent diabetes mellitus at 11 years old with early onset of renal impairment, proteinuria and hypertension. Urinary tract dilatation was demonstrated in both patients. Kidney biopsies were compatible with diabetic nephropathy. Both children also had bilateral sensorineural hearing loss. Optic atrophy with severe loss of vision was detected in the girl and bilateral cataract in her brother. Both patients were HLA DR2 positive. At 16 years old, her creatinine clearance was 16 ml/min/1.73 m2. Her brother's creatinine clearance was 25 ml/min/1.73 m2 at 13 years old. We conclude that renal function should be evaluated in patients with Wolfram syndrome and the cause of renal failure in these patients may be rapid and severe diabetic nephropathy.


Subject(s)
Diabetic Nephropathies/pathology , Glomerular Mesangium/pathology , HLA Antigens/genetics , Renal Insufficiency/pathology , Wolfram Syndrome/complications , Biopsy , Child , Female , Humans , Karyotyping , Male , Wolfram Syndrome/immunology
7.
Diabetes Res Clin Pract ; 22(2-3): 175-80, 1994 Jan.
Article in English | MEDLINE | ID: mdl-8200299

ABSTRACT

The Wolfram syndrome (WS) is an autosomal recessive disorder beginning in childhood that consists of four clinical features: diabetes insipidus, diabetes mellitus, optic atrophy and deafness. Its pathogenesis remains unknown, although the tendency to develop this syndrome has been related to some class II antigens of the HLA system. We report six new cases in four families. A review of published data from the genetic features of this syndrome is performed, establishing the high frequency of the HLA-DR2 antigen in the WS (44.4%) compared with a control group (21.9%; relative risk, 2.8) and to patients with Type 1 insulin-dependent diabetes mellitus (Type 1 diabetes) (6.77%; relative risk, 9.7). We also comment the high frequency of the HLA-DQw1 antigen (85.5%) in this syndrome, without statistical significance. A familial segregation study of the HLA haplotypes has been carried out without finding correlation between the autosomal recessive pattern attributed to the WS, and the major histocompatibility complex. In conclusion, whereas HLA may increase susceptibility to the WS, as shown by the existence of an HLA-DR2 association, the major genetic influence on the inheritance of the WS must be at another locus.


Subject(s)
HLA Antigens/genetics , HLA-DR Antigens/genetics , Wolfram Syndrome/genetics , Wolfram Syndrome/immunology , Female , HLA Antigens/blood , HLA-DR Antigens/blood , Haplotypes/genetics , Humans , Male , Nuclear Family , Pedigree
10.
Acta Paediatr Scand ; 77(3): 413-8, 1988 May.
Article in English | MEDLINE | ID: mdl-3291550

ABSTRACT

The Wolfram, or DIDMOAD, syndrome is a rare congenital disease that is associated with diabetes insipidus, insulin dependent diabetes mellitus of an early onset, bilateral optic atrophy and deafness. Urological disorders are usually present as well. We have studied nine patients belonging to five different families. All of the family members were HLA typed (including DR), and islet cell as well as antinuclear antibody determinations were carried out. Although individuals with insulin dependent diabetes mellitus are very prone to have either HLA-DR3 or -DR4 antigens, none of our patients had DR3 antigens and only one was DR4 positive. On the other hand, three of our patients were typed as HLA-DR2 positive. This antigen is uncommon in classical insulin dependent diabetes. In one of the families, the affected siblings did not share the same HLA haplotype. Islet cell and antinuclear antibodies were not found in any of the cases and six of the patients had a small, but significant, insulin secretory reserve. On the basis of some of the clinical features it was also possible to further distinguish between the DIDMOAD syndrome and the classical insulin dependent diabetes mellitus. The differences encountered between classical and DIDMOAD insulin dependent diabetes mellitus--the presence/absence of HLA linkage, HLA-DR2, -DR3 and -DR4 associations, islet cell or antinuclear antibodies, the tendency to ketosis and diabetic retinopathy--indicate that their etiopathogenies are triggered by distinct mechanisms.


Subject(s)
Ectodermal Dysplasia/genetics , Wolfram Syndrome/genetics , Adolescent , Adult , Antibodies, Antinuclear/analysis , Child , Ectodermal Dysplasia/immunology , Female , HLA Antigens/genetics , HLA-A Antigens , HLA-B Antigens , HLA-DR Antigens/genetics , Haploidy , Humans , Islets of Langerhans/immunology , Male , Spain , Wolfram Syndrome/immunology
11.
Ophthalmic Paediatr Genet ; 9(1): 25-8, 1988 Mar.
Article in English | MEDLINE | ID: mdl-3043304

ABSTRACT

A Sicilian family with three siblings affected by Wolfram's syndrome (Ws) is reported. HLA typing was performed in eight individuals from this family through three generations. Two of the three patients were HLA DR2 positive. The results suggest that the gene for Ws is not linked to the HLA region on chromosome 6, but located on some other chromosome, and that the allele HLA DR2 might predispose to the mutation responsible for Ws.


Subject(s)
HLA Antigens/classification , Wolfram Syndrome/immunology , Adolescent , Child , Child, Preschool , Genotype , HLA Antigens/analysis , Humans , Male , Pedigree , Wolfram Syndrome/genetics
16.
Diabetes Care ; 9(4): 405-8, 1986.
Article in English | MEDLINE | ID: mdl-3461931

ABSTRACT

The Wolfram, or DIDMOAD, syndrome consists of diabetes insipidus, diabetes mellitus, optic atrophy, and deafness. Diabetes mellitus usually occurs as the first manifestation of this syndrome, followed by the development of optic atrophy, neurosensory hearing loss, and finally diabetes insipidus. We report on four cases with a review of the literature. The diabetes mellitus occurring in these patients is clinically indistinguishable from classic type I diabetes mellitus. Two of three patients continue to have measurable C-peptide secretion 8 yr after onset of diabetes. Two of three patients with Wolfram syndrome had the HLA-DR2 antigen. Combining our cases with those described in the literature, 7 of 11 patients have the HLA-DR2 antigen. The preponderance of the HLA-DR2 antigen in the Wolfram syndrome is different from classic type I diabetes. This is further evidence of the genetic heterogeneity of diabetes mellitus. Although the Wolfram syndrome is rare, it should be considered in diabetic patients with unexplained optic atrophy and hearing loss or with polyuria and polydipsia in the presence of adequate blood sugar control.


Subject(s)
Wolfram Syndrome/physiopathology , Adolescent , Adult , Child , Child, Preschool , Diabetes Mellitus, Type 1/diagnosis , Diagnosis, Differential , Female , HLA-DR Antigens , Histocompatibility Antigens Class II/analysis , Humans , Male , Wolfram Syndrome/diagnosis , Wolfram Syndrome/immunology
17.
Arch Dis Child ; 60(9): 823-8, 1985 Sep.
Article in English | MEDLINE | ID: mdl-4051539

ABSTRACT

Seven patients with a rare syndrome of diabetes insipidus (DI), diabetes mellitus (DM), optic atrophy (OA), neurosensory deafness (D), atony of the urinary tract, and other abnormalities (Wolfram or DIDMOAD syndrome) are reported. Of the seven patients, three siblings were followed up for 10-17 years. All seven patients had diabetes mellitus and optic atrophy; six had diabetes insipidus; and in the four patients investigated there was dilatation of the urinary tract. The severity of diabetes varied, and all required insulin for control of the hyperglycaemia. In one patient the course of the disease simulated maturity onset diabetes of the young; another presented with ketoacidosis; but none had haplotypes usually associated with insulin dependent diabetes mellitus. The diabetes insipidus responded to chlorpropamide, suggesting partial antidiuretic hormone deficiency. Onset of optic atrophy and loss of vision occurred relatively late and progressed slowly, although in one patient there was a rapid deterioration in visual acuity. Deafness was mild, of late onset, and of sensorineural origin. A degenerative process affecting the central and peripheral nervous system can explain all the manifestations of the syndrome except diabetes mellitus. The pathogenesis of the diabetes mellitus remains obscure.


Subject(s)
Wolfram Syndrome/diagnosis , Child , Child, Preschool , Diabetes Insipidus/diagnosis , Diabetes Mellitus, Type 1/diagnosis , Female , HLA Antigens/analysis , Hearing Loss, Sensorineural/diagnosis , Humans , Male , Optic Atrophy/diagnosis , Wolfram Syndrome/genetics , Wolfram Syndrome/immunology
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