Genetic basis of early-onset, maturity-onset diabetes of the young-like diabetes in Japan and features of patients without mutations in the major MODY genes: Dominance of maternal inheritance

被引:27
作者
Yorifuji, Tohru [1 ,2 ,3 ]
Higuchi, Shinji [1 ]
Kawakita, Rie [1 ,2 ]
Hosokawa, Yuki [1 ]
Aoyama, Takane [2 ]
Murakami, Akiko [2 ]
Kawae, Yoshiko [3 ]
Hatake, Kazue [3 ]
Nagasaka, Hironori [4 ]
Tamagawa, Nobuyoshi [2 ]
机构
[1] Osaka City Gen Hosp, Div Pediat Endocrinol & Metab, Childrens Med Ctr, 2-13-22 Miyakojima Hondori, Miyakojima, Osaka 5340021, Japan
[2] Osaka City Gen Hosp, Dept Genet Med, Osaka, Japan
[3] Osaka City Gen Hosp, Clin Res Ctr, Osaka, Japan
[4] Takarazuka City Hosp, Dept Pediat, Takarazuka, Hyogo, Japan
关键词
inheritance; Japanese; MODY; type; 2; diabetes; CLINICAL-DIAGNOSIS; IDENTIFICATION; VARIANTS; FAMILY; HNF1A; HNF4A; RISK; GCK;
D O I
10.1111/pedi.12714
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Causative mutations cannot be identified in the majority of Asian patients with suspected maturity-onset diabetes of the young (MODY). Objectives: To elucidate the genetic basis of Japanese patients with MODY-like diabetes and gain insight into the etiology of patients without mutations in the major MODY genes. Subjects: A total of 263 Japanese patients with early-onset, non-obese, MODY-like diabetes mellitus referred to Osaka City General Hospital for diagnosis. Methods: Mutational analysis of the four major MODY genes (GCK, HNF1A, HNF4A, HNF1B) by Sanger sequencing. Mutation-positive and mutation-negative patients were further analyzed for clinical features. Results: Mutations were identified in 103 (39.2%) patients; 57 mutations in GCK; 29, HNF1A; 7, HNF4A; and 10, HNF1B. Contrary to conventional diagnostic criteria, 18.4% of mutation-positive patients did not have affected parents and 8.2% were in the overweight range (body mass index [BMI] >85th percentile). HOMA-IR at diagnosis was elevated (>2) in 15 of 66 (22.7%) mutation-positive patients. Compared with mutation-positive patients, mutation-negative patients were significantly older (P=0.003), and had higher BMI percentile at diagnosis (P=0.0006). Interestingly, maternal inheritance of diabetes was significantly more common in mutation-negative patients (P = 0.0332) and these patients had significantly higher BMI percentile as compared with mutation-negative patients with paternal inheritance (P = 0.0106). Conclusions: Contrary to the conventional diagnostic criteria, de novo diabetes, overweight, and insulin-resistance are common in Japanese patients with mutation-positive MODY. A significant fraction of mutation-negative patients had features of early-onset type 2 diabetes common in Japanese, and non-Mendelian inheritance needs to be considered for these patients.
引用
收藏
页码:1164 / 1172
页数:9
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