Suppr超能文献

HNF1A 基因 p.I27L 与土耳其的早发、成年发病的青年型相似糖尿病相关。

HNF1A gene p.I27L is associated with early-onset, maturity-onset diabetes of the young-like diabetes in Turkey.

机构信息

Department of Endocrinology and Metabolism, Diskapi Yildirim Beyazit Teaching and Training Research Hospital, Ankara, Turkey.

Department of Medical Biology, Baskent University, Ankara, Turkey.

出版信息

BMC Endocr Disord. 2019 May 20;19(1):51. doi: 10.1186/s12902-019-0375-2.

Abstract

BACKGROUND

The molecular basis of the Turkish population with suspected maturity-onset diabetes of the young (MODY) has not been identified. This is the first study to investigate the association between HNF1A-gene single-nucleotide polymorphisms (SNPs) and having early-onset, MODY-like diabetes mellitus in the Turkish population.

METHODS

All diabetic patients (N = 565) who presented to our clinic between 2012 and 2015 with a clinical suspicion of MODY were included in the study. Analysis of HNF1A, HNFB, HNF4A, GCK gene mutations was performed using real-time polymerase chain reaction sequencing. After genetic analysis, diabetics (n = 46) with HNF1A, HNF1B, HNF4A, GCK gene mutations (diagnosed as MODY) and diabetics (n = 30) with HNF1B, HNF4A, GCK gene SNPs were excluded. Patients with early-onset, MODY-like diabetes (n = 486) and non-diabetic controls (n = 263) were included. Genetic analyses for the HNF1A gene p.S487 N (rs2464196), p.A98V (rs1800574) and p.I27L (rs1169288) SNPs were performed using Sanger-based DNA sequencing among the control group.

RESULTS

p.S487 N and p.A98V was similar between the diabetics and controls in dominant and recessive models with no association (each, p > 0.05). p.I27L GT/TT carriers (GT/TT vs. GG, OR = 1.68, 95% CI: [1. 21-2.13]; p = 0.035) and p.I27L TT carriers had increased risk of having MODY-like diabetes (GT/GG vs. TT, OR = 1.56, 95% CI: [1. 14-2.57]; p = 0.048). Family inheritance of diabetes was significantly more common in patients with the p.I27L TT genotype. The p.I27L SNP was modestly associated with having diabetes after adjusting for body mass index and age (β = 1.45, 95% CI: [1. 2-4.2]; p = 0.036).

CONCLUSIONS

The HNF1A gene p.I27L SNP was modestly associated with having early-onset, MODY-like diabetes in the Turkish population. HNF1A gene p.I27L SNP might contribute to age at diabetes diagnosis and family inheritance.

摘要

背景

疑似青年起病的成年型糖尿病(MODY)的土耳其人群的分子基础尚未确定。这是第一项研究,旨在调查 HNF1A 基因单核苷酸多态性(SNPs)与土耳其人群中早发、MODY 样糖尿病之间的关联。

方法

所有在 2012 年至 2015 年间因疑似 MODY 而就诊于我院的糖尿病患者(N=565)均纳入本研究。采用实时聚合酶链反应测序分析 HNF1A、HNFB、HNF4A、GCK 基因突变。进行基因分析后,排除 HNF1A、HNF1B、HNF4A、GCK 基因突变(诊断为 MODY)的糖尿病患者(n=46)和 HNF1B、HNF4A、GCK 基因 SNPs 的糖尿病患者(n=30)。纳入早发、MODY 样糖尿病患者(n=486)和非糖尿病对照者(n=263)。在对照组中,采用 Sanger 测序法对 HNF1A 基因 p.S487N(rs2464196)、p.A98V(rs1800574)和 p.I27L(rs1169288)SNP 进行基因分析。

结果

在显性和隐性模型中,糖尿病患者和对照组的 p.S487N 和 p.A98V 无差异(各 p>0.05)。p.I27L GT/TT 携带者(GT/TT 与 GG,OR=1.68,95%CI:[1.21-2.13];p=0.035)和 p.I27L TT 携带者发生 MODY 样糖尿病的风险增加(GT/GG 与 TT,OR=1.56,95%CI:[1.14-2.57];p=0.048)。p.I27L TT 基因型患者糖尿病家族遗传更为常见。调整体重指数和年龄后,p.I27L SNP 与糖尿病的发生有中度相关性(β=1.45,95%CI:[1.2-4.2];p=0.036)。

结论

HNF1A 基因 p.I27L SNP 与土耳其人群中早发、MODY 样糖尿病有中度相关性。HNF1A 基因 p.I27L SNP 可能导致糖尿病的发病年龄和家族遗传。

相似文献

2
The Common Variant I27L Is a Modifier of Age at Diabetes Diagnosis in Individuals With HNF1A-MODY.
Diabetes. 2018 Sep;67(9):1903-1907. doi: 10.2337/db18-0133. Epub 2018 Jun 12.
4
HNF1A gene p.I27L is associated with co-existing preeclampsia in gestational diabetes mellitus.
Gynecol Endocrinol. 2020 Jun;36(6):530-534. doi: 10.1080/09513590.2019.1698023. Epub 2019 Dec 11.
6
Associations between the common HNF1A gene variant p.I27L (rs1169288) and risk of type 2 diabetes mellitus are influenced by weight.
Diabetes Metab. 2015 Feb;41(1):91-4. doi: 10.1016/j.diabet.2014.04.009. Epub 2014 Jun 2.
9
Maturity onset diabetes of the young (MODY) in Chinese children: genes and clinical phenotypes.
J Pediatr Endocrinol Metab. 2019 Jul 26;32(7):759-765. doi: 10.1515/jpem-2018-0446.
10
Evaluation of serum 1,5 anhydroglucitol levels as a clinical test to differentiate subtypes of diabetes.
Diabetes Care. 2010 Feb;33(2):252-7. doi: 10.2337/dc09-1246. Epub 2009 Nov 23.

引用本文的文献

1
(rs11605924) and (rs560887) single nucleotide polymorphisms increase risk of type 2 diabetes mellitus.
Biomed Rep. 2025 Jun 19;23(3):144. doi: 10.3892/br.2025.2022. eCollection 2025 Sep.
3
VARIATIONS IN MONOGENIC DIABETES AND DIABETES SUSCEPTIBILITY GENES IN PEDIATRIC CASES: SINGLE CENTER EXPERIENCE.
Acta Endocrinol (Buchar). 2023 Oct-Dec;19(4):512-522. doi: 10.4183/aeb.2023.512. Epub 2024 Jun 24.
6
Identification and management of GCK-MODY complicating pregnancy in Chinese patients with gestational diabetes.
Mol Cell Biochem. 2022 May;477(5):1629-1643. doi: 10.1007/s11010-022-04374-8. Epub 2022 Feb 28.
7
When do we need to suspect maturity onset diabetes of the young in patients with type 2 diabetes mellitus?
Arch Endocrinol Metab. 2022 Mar 8;66(1):32-39. doi: 10.20945/2359-3997000000431. Epub 2022 Jan 13.
8
Transcriptomic analysis of elderly women with low muscle mass: association with immune system pathway.
Aging (Albany NY). 2021 Sep 7;13(17):20992-21008. doi: 10.18632/aging.203505.
9
Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical Investigation.
Front Endocrinol (Lausanne). 2021 Jul 29;12:684018. doi: 10.3389/fendo.2021.684018. eCollection 2021.

本文引用的文献

2
The Common Variant I27L Is a Modifier of Age at Diabetes Diagnosis in Individuals With HNF1A-MODY.
Diabetes. 2018 Sep;67(9):1903-1907. doi: 10.2337/db18-0133. Epub 2018 Jun 12.
4
Structure-function studies of HNF1A (MODY3) gene mutations in South Indian patients with monogenic diabetes.
Clin Genet. 2016 Dec;90(6):486-495. doi: 10.1111/cge.12757. Epub 2016 Mar 4.
6
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.
Nat Genet. 2015 Dec;47(12):1415-25. doi: 10.1038/ng.3437. Epub 2015 Nov 9.
7
Associations between the common HNF1A gene variant p.I27L (rs1169288) and risk of type 2 diabetes mellitus are influenced by weight.
Diabetes Metab. 2015 Feb;41(1):91-4. doi: 10.1016/j.diabet.2014.04.009. Epub 2014 Jun 2.
9
Approach to the patient with atypical diabetes.
CMAJ. 2014 Jun 10;186(9):678-84. doi: 10.1503/cmaj.130185. Epub 2014 Jan 6.
10
Variants of the HNF1α gene: A molecular approach concerning diabetic patients from southern Brazil.
Genet Mol Biol. 2012 Dec;35(4):737-40. doi: 10.1590/S1415-47572012005000061. Epub 2012 Oct 9.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验