Literature DB >> 34487217

Genotype-phenotype correlations and response to glucose lowering therapy in subjects with HNF1β associated diabetes.

Nicholas Ng1, Matilde Mijares Zamuner2, Najia Siddique2, Joon Kim2, Marie Burke2, Maria Michele Byrne2.   

Abstract

AIMS: Molecular defects of hepatic nuclear factor 1β (HNF1β) are associated with multiorgan disease (renal disease, pancreatic hypoplasia, and genital tract anomalies) in addition to diabetes. We examined the phenotypic features, insulin secretory response to glucose, and response to treatment in subjects with HNF1β-MODY (MODY 5).
METHODS: Twelve subjects with HNF1β-MODY were phenotyped in detail. A 2-h oral glucose tolerance test was performed to establish insulin secretory response with glucose, insulin and C-peptide measurements taken at baseline and 30 min intervals. Clinical follow-up occurred bi-annually.
RESULTS: Ten of 12 subjects had diabetes with mean age of onset of 30.2 ± 15.5 years, fasting glucose of 9.7 ± 4.6 mmol/L and HbA1c of 60.9 ± 17.1 mmol/mol (7.7 ± 1.6%). Renal and/or pancreatic morphological abnormalities were found in 9 subjects. Mean fasting C-peptide (0.5 ± 0.4 nmol/L) and AUC C-peptide (1.5 ± 1.0 nmol/L/120 min) were reduced in our cohort with 4 subjects demonstrating marked insulin deficiency. OGIS was reduced at 290.2 ± 67.0 ml min-1 m-2. 6/10 subjects were on insulin therapy at initial diagnosis and 8/10 at last clinical follow-up. Mean insulin dose at last clinical follow-up was 0.45 ± 0.23units/kg/day. 5 subjects on insulin were trialled on sulphonylurea therapy, and none was successfully weaned off insulin.
CONCLUSIONS: Diagnosing HNF1β-MODY in a diabetes clinic is challenging due to its variable phenotype and variable age of onset. β-Cell dysfunction and insulin resistance contribute to diabetes in HNF1β-MODY. No subjects successfully transitioned to sulphonylurea. Early initiation of insulin therapy would be suitable to achieve glycaemic control. This emphasizes the importance of genetic testing for monogenic forms of diabetes to guide personalized treatment.
© 2021. Springer-Verlag Italia S.r.l., part of Springer Nature.

Entities:  

Keywords:  HNF1B; HNF1B diabetes; Insulin; MODY; Sulphonylurea; Treatment

Mesh:

Substances:

Year:  2021        PMID: 34487217     DOI: 10.1007/s00592-021-01794-8

Source DB:  PubMed          Journal:  Acta Diabetol        ISSN: 0940-5429            Impact factor:   4.280


  31 in total

Review 1.  Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young.

Authors:  S S Fajans; G I Bell; K S Polonsky
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4.  A novel syndrome of diabetes mellitus, renal dysfunction and genital malformation associated with a partial deletion of the pseudo-POU domain of hepatocyte nuclear factor-1beta.

Authors:  T H Lindner; P R Njolstad; Y Horikawa; L Bostad; G I Bell; O Sovik
Journal:  Hum Mol Genet       Date:  1999-10       Impact factor: 6.150

5.  Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY.

Authors:  Y Horikawa; N Iwasaki; M Hara; H Furuta; Y Hinokio; B N Cockburn; T Lindner; K Yamagata; M Ogata; O Tomonaga; H Kuroki; T Kasahara; Y Iwamoto; G I Bell
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8.  HNF1B deletions in patients with young-onset diabetes but no known renal disease.

Authors:  E L Edghill; K Stals; R A Oram; M H Shepherd; A T Hattersley; S Ellard
Journal:  Diabet Med       Date:  2013-01       Impact factor: 4.359

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Authors:  Silvia Ferrè; Ernie M H F Bongers; Ramon Sonneveld; Elisabeth A M Cornelissen; Johan van der Vlag; Gerben A J van Boekel; Jack F M Wetzels; Joost G J Hoenderop; René J M Bindels; Tom Nijenhuis
Journal:  J Clin Endocrinol Metab       Date:  2013-08-26       Impact factor: 5.958

10.  Systematic Population Screening, Using Biomarkers and Genetic Testing, Identifies 2.5% of the U.K. Pediatric Diabetes Population With Monogenic Diabetes.

Authors:  Maggie Shepherd; Beverley Shields; Suzanne Hammersley; Michelle Hudson; Timothy J McDonald; Kevin Colclough; Richard A Oram; Bridget Knight; Christopher Hyde; Julian Cox; Katherine Mallam; Christopher Moudiotis; Rebecca Smith; Barbara Fraser; Simon Robertson; Stephen Greene; Sian Ellard; Ewan R Pearson; Andrew T Hattersley
Journal:  Diabetes Care       Date:  2016-06-06       Impact factor: 19.112

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