Prevalence and Clinical Characteristics of PDX1 Variant Induced Diabetes in Chinese Early-Onset Type 2 Diabetes

Author:

Lian Hong1ORCID,Gong Siqian1,Li Meng1,Wang Xirui2,Wang Fang3,Cai Xiaoling1,Liu Wei1,Luo Yingying1,Zhang Simin1,Zhang Rui1,Zhou Lingli1,Zhu Yu1,Ma Yumin1,Ren Qian1ORCID,Zhang Xiuying1,Chen Jing1,Chen Ling1,Wu Jing1,Gao Leili1,Zhou Xianghai1,Li Yufeng4ORCID,Zhong Liyong3,Han Xueyao1ORCID,Ji Linong1ORCID

Affiliation:

1. Department of Endocrinology and Metabolism, Peking University People's Hospital, Peking University Diabetes Center. No. 11 , Beijing 100044 , China

2. Department of Endocrinology, Beijing Airport Hospital. No. 49 , Beijing 101318 , China

3. Department of Endocrinology, Capital Medical University Beijing Tiantan Hospital. No. 119 , Beijing 100050 , China

4. Department of Endocrinology, Beijing Pinggu Hospital. No. 59 , Beijing 101200 , China

Abstract

Abstract Context Maturity-onset diabetes of the young 4 (MODY4) is caused by mutations of PDX1; its prevalence and clinical features are not well known. Objective This study aimed to investigate the prevalence and clinical characteristics of MODY4 in Chinese people clinically diagnosed with early-onset type 2 diabetes (EOD), and to evaluate the relationship between the PDX1 genotype and the clinical phenotype. Method The study cohort consisted of 679 patients with EOD. PDX1 mutations were screened by DNA sequencing, and their pathogenicity was evaluated by functional experiments and American College of Medical Genetics and Genomics guidelines. MODY4 was diagnosed in individuals with diabetes who carry a pathogenic or likely pathogenic PDX1 variant. All reported cases were reviewed for analyzing the genotype–phenotype relationship. Result 4 patients with MODY4 were identified, representing 0.59% of this Chinese EOD cohort. All the patients were diagnosed before 35 years old, either obese or not obese. Combined with previously reported cases, the analysis revealed that the carriers of homeodomain variants were diagnosed earlier than those with transactivation domain variants (26.10 ± 11.00 vs 41.85 ± 14.66 years old, P < .001), and the proportions of overweight and obese individuals with missense mutation were higher than those with nonsense or frameshift mutations (27/34 [79.4%] vs 3/8 [37.5%], P = .031). Conclusion Our study suggested that MODY4 was prevalent in 0.59% of patients with EOD in a Chinese population. It was more difficult to identify clinically than other MODY subtypes owning to its clinical similarity to EOD. Also, this study revealed that there is some relationship between genotype and phenotype.

Funder

National Key R&D Program of China

Beijing Science and Technology Committee Fund

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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