Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2016 Oct;40(5):455-461.
doi: 10.1016/j.jcjd.2015.12.005. Epub 2016 Apr 18.

Searching for Maturity-Onset Diabetes of the Young (MODY): When and What for?

Affiliations
Review

Searching for Maturity-Onset Diabetes of the Young (MODY): When and What for?

José Timsit et al. Can J Diabetes. 2016 Oct.

Abstract

Maturity-onset diabetes of the young (MODY) is a group of monogenic diseases that results in primary defects in insulin secretion and dominantly inherited forms of nonautoimmune diabetes. Although many genes may be associated with monogenic diabetes, heterozygous mutations in 6 of them are responsible for the majority of cases of MODY. Glucokinase (GCK)-MODY is due to mutations in the glucokinase gene, 3 MODY subtypes are associated with mutations in the hepatocyte nuclear factor (HNF) transcription factors, and 2 others with mutations in ABCC8 and KCNJ11, which encode the subunits of the ATP-dependent potassium channel in pancreatic beta cells. GCK-MODY and HNF1A-MODY are the most common subtypes. The clinical presentation of MODY subtypes has been reported to differ according to the gene involved, and the diagnosis of MODY may be considered in various clinical circumstances. However, except in patients with GCK-MODY whose phenotype is very homogeneous, in most cases the penetrance and expressivity of a given molecular abnormality vary greatly among patients and, conversely, alterations in various genes may lead to similar phenotypes. Moreover, differential diagnosis among more common forms of diabetes may be difficult, particularly with type 2 diabetes. Thus, careful assessment of the personal and family histories of patients with diabetes is mandatory to select those in whom genetic screening is worthwhile. The diagnosis of monogenic diabetes has many consequences in terms of prognosis, therapeutics and family screening.

Keywords: canal potassique; deletion; diabète de la maturité chez le sujet jeune (MODY); diabète monogénique; délétion; facteur nucléaire des hépatocytes; glucokinase; hepatocyte nuclear factor; maturity-onset diabetes of the young (MODY); monogenic diabetes; potassium channel.

PubMed Disclaimer

Similar articles

Cited by

  • Variants influencing age at diagnosis of HNF1A-MODY.
    Ludwig-Słomczyńska AH, Seweryn MT, Radkowski P, Kapusta P, Machlowska J, Pruhova S, Gasperikova D, Bellanne-Chantelot C, Hattersley A, Kandasamy B, Letourneau-Freiberg L, Philipson L, Doria A, Wołkow PP, Małecki MT, Klupa T. Ludwig-Słomczyńska AH, et al. Mol Med. 2022 Sep 14;28(1):113. doi: 10.1186/s10020-022-00542-0. Mol Med. 2022. PMID: 36104811 Free PMC article.
  • A1C: Episode 1.
    Aung NL. Aung NL. Clin Diabetes. 2024 Winter;42(1):165-168. doi: 10.2337/cd23-0084. Epub 2023 Oct 24. Clin Diabetes. 2024. PMID: 38230343 No abstract available.
  • Agnostic Pathway/Gene Set Analysis of Genome-Wide Association Data Identifies Associations for Pancreatic Cancer.
    Walsh N, Zhang H, Hyland PL, Yang Q, Mocci E, Zhang M, Childs EJ, Collins I, Wang Z, Arslan AA, Beane-Freeman L, Bracci PM, Brennan P, Canzian F, Duell EJ, Gallinger S, Giles GG, Goggins M, Goodman GE, Goodman PJ, Hung RJ, Kooperberg C, Kurtz RC, Malats N, LeMarchand L, Neale RE, Olson SH, Scelo G, Shu XO, Van Den Eeden SK, Visvanathan K, White E, Zheng W; PanScan and PanC4 consortia; Albanes D, Andreotti G, Babic A, Bamlet WR, Berndt SI, Borgida A, Boutron-Ruault MC, Brais L, Brennan P, Bueno-de-Mesquita B, Buring J, Chaffee KG, Chanock S, Cleary S, Cotterchio M, Foretova L, Fuchs C, M Gaziano JM, Giovannucci E, Goggins M, Hackert T, Haiman C, Hartge P, Hasan M, Helzlsouer KJ, Herman J, Holcatova I, Holly EA, Hoover R, Hung RJ, Janout V, Klein EA, Kurtz RC, Laheru D, Lee IM, Lu L, Malats N, Mannisto S, Milne RL, Oberg AL, Orlow I, Patel AV, Peters U, Porta M, Real FX, Rothman N, Sesso HD, Severi G, Silverman D, Strobel O, Sund M, Thornquist MD, Tobias GS, Wactawski-Wende J, Wareham N, Weiderpass E, Wentzensen N, Wheeler W, Yu H, Zeleniuch-Jacquotte A, Kraft P, Li D, Jacobs EJ, Petersen GM, Wolpin BM, Risch HA, Amundadottir LT, Yu K, Klein AP, Stolzenberg-Solomon RZ. Walsh N, et al. J Natl Cancer Inst. 2019 Jun 1;111(6):557-567. doi: 10.1093/jnci/djy155. J Natl Cancer Inst. 2019. PMID: 30541042 Free PMC article.
  • Hyperglycemia in pediatric age: could it be maturity onset diabetes of the young? Case reports and review of the literature.
    Cascais M, Pereira E, Vieira A, Venâncio M, Ramos L, Moleiro P. Cascais M, et al. Ann Pediatr Endocrinol Metab. 2019 Dec;24(4):262-266. doi: 10.6065/apem.2019.24.4.262. Epub 2019 Dec 31. Ann Pediatr Endocrinol Metab. 2019. PMID: 31905448 Free PMC article.
  • Molecular Dynamics Simulation of Kir6.2 Variants Reveals Potential Association with Diabetes Mellitus.
    Elangeeb ME, Elfaki I, Eleragi AMS, Ahmed EM, Mir R, Alzahrani SM, Bedaiwi RI, Alharbi ZM, Mir MM, Ajmal MR, Tayeb FJ, Barnawi J. Elangeeb ME, et al. Molecules. 2024 Apr 22;29(8):1904. doi: 10.3390/molecules29081904. Molecules. 2024. PMID: 38675722 Free PMC article.

MeSH terms

LinkOut - more resources