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When do we need to suspect maturity onset diabetes of the young in patients with type 2 diabetes mellitus?
Üstay, Özlem; Apaydin, Tugçe; Elbasan, Onur; Polat, Hamza; Günhan, Gizem; Dinçer, Ceyda; Seker, Lamia; Ates, Esra Arslan; Yabaci, Aysegül; Güney, Ahmet lter; Yavuz, Dilek Gogas.
  • Üstay, Özlem; Marmara University School of Medicine, Endocrinology and Metabolism. Istanbul. TR
  • Apaydin, Tugçe; Marmara University School of Medicine, Endocrinology and Metabolism. Istanbul. TR
  • Elbasan, Onur; Marmara University School of Medicine, Endocrinology and Metabolism. Istanbul. TR
  • Polat, Hamza; Marmara University School of Medicine. Istanbul. TR
  • Günhan, Gizem; Marmara University School of Medicine. Istanbul. TR
  • Dinçer, Ceyda; Marmara University School of Medicine, Endocrinology and Metabolism. Istanbul. TR
  • Seker, Lamia; Marmara University School of Medicine. Istanbul. TR
  • Ates, Esra Arslan; Marmara University School of Medicine. Istanbul. TR
  • Yabaci, Aysegül; Bezmialem Vakif University School of Medicine. Department of Biostatistics. Istanbul. TR
  • Güney, Ahmet lter; Marmara University School of Medicine. Istanbul. TR
  • Yavuz, Dilek Gogas; Marmara University School of Medicine, Endocrinology and Metabolism. Istanbul. TR
Arch. endocrinol. metab. (Online) ; 66(1): 32-39, Jan.-Feb. 2022. tab
Article in English | LILACS | ID: biblio-1364313
ABSTRACT
ABSTRACT

Objetivo:

Maturity onset diabetes of the young (MODY) patients have clinical heterogeneity as shown by many studies. Thus, often it is misdiagnosed to type 1 or type 2 diabetes(T2DM). The aim of this study is to evaluate MODY mutations in adult T2DM patients suspicious in terms of MODY, and to show clinical and laboratory differences between these two situations. Subjects and

methods:

In this study, we analyzed 72 type 2 diabetic patients and their relatives (35F/37M) who had been suspected for MODY and referred to genetic department for mutation analysis. The gene mutations for MODY have been assessed in the laboratory of Marmara University genetics. Totally 67 (32F/35M; median age 36.1) diabetic patients were analyzed for 7 MODY mutations. Twelve patients who have uncertain mutation (VUS) were excluded from study for further evaluation. MODY(+) (n30) patients and T2DM patients (n25) were compared for clinical and laboratory parameters.

Results:

In MODY(+) subjects, mutations in GCK (MODY 2) (n12; 40%) were the most common followed by HNF4A (MODY 1) (n4; 13.3%). Diabetes diagnosis age was younger in MODY(+) group but not statistically significant. Sixty-six percent of MODY(+) subjects had diabetes history at 3-consecutive generations in their family compared with 28% of T2DM patients statistically significant (p0.006). Gender, BMI, C-peptide, HbA1c, lipid parameters, creatinine, GFR, microalbuminuria, vitamin D and calcium were not statistically different between the groups.

Conclusion:

According to present study results, MODY mutation positivity is most probable in young autoantibody (-) diabetic patients diagnosed before 30 years of age, who have first degree family history of diabetes.
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Diabetes Mellitus, Type 2 Limits: Adult / Humans Language: English Journal: Arch. endocrinol. metab. (Online) Journal subject: Endocrinology / Metabolism Year: 2022 Type: Article Affiliation country: Turkey Institution/Affiliation country: Bezmialem Vakif University School of Medicine/TR / Marmara University School of Medicine/TR / Marmara University School of Medicine, Endocrinology and Metabolism/TR

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Full text: Available Index: LILACS (Americas) Main subject: Diabetes Mellitus, Type 2 Limits: Adult / Humans Language: English Journal: Arch. endocrinol. metab. (Online) Journal subject: Endocrinology / Metabolism Year: 2022 Type: Article Affiliation country: Turkey Institution/Affiliation country: Bezmialem Vakif University School of Medicine/TR / Marmara University School of Medicine/TR / Marmara University School of Medicine, Endocrinology and Metabolism/TR