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

被引:5
作者
Lian, Hong [1 ]
Gong, Siqian [1 ]
Li, Meng [1 ]
Wang, Xirui [2 ]
Wang, Fang [3 ]
Cai, Xiaoling [1 ]
Liu, Wei [1 ]
Luo, Yingying [1 ]
Zhang, Simin [1 ]
Zhang, Rui [1 ]
Zhou, Lingli [1 ]
Zhu, Yu [1 ]
Ma, Yumin [1 ]
Ren, Qian [1 ]
Zhang, Xiuying [1 ]
Chen, Jing [1 ]
Chen, Ling [1 ]
Wu, Jing [1 ]
Gao, Leili [1 ]
Zhou, Xianghai [1 ]
Li, Yufeng [4 ]
Zhong, Liyong [3 ]
Han, Xueyao [1 ]
Ji, Linong [1 ]
机构
[1] Peking Univ, Peoples Hosp, Diabet Ctr 11, Dept Endocrinol & Metab, Beijing 100044, Peoples R China
[2] Beijing Airport Hosp 49, Dept Endocrinol, Beijing 101318, Peoples R China
[3] Capital Med Univ, Beijing Tiantan Hosp 119, Dept Endocrinol, Beijing 100050, Peoples R China
[4] Beijing Pinggu Hosp 59, Dept Endocrinol, Beijing 101200, Peoples R China
关键词
type; 2; diabetes; PDX1; MODY4; genotype; phenotype; YOUNG MODY; DIAGNOSIS; IDENTIFICATION; MUTATIONS; PHENOTYPE; AGENESIS; SEARCH; ADULTS;
D O I
10.1210/clinem/dgad303
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:E1644 / E1652
页数:9
相关论文
共 46 条
  • [1] Neonatal diabetes mellitus
    Aguilar-Bryan, Lydia
    Bryan, Joseph
    [J]. ENDOCRINE REVIEWS, 2008, 29 (03) : 265 - 291
  • [2] β-cell-specific inactivation of the mouse Ipf1/Pdx1 gene results in loss of the β-cell phenotype and maturity onset diabetes
    Ahlgren, U
    Jonsson, J
    Jonsson, L
    Simu, K
    Edlund, H
    [J]. GENES & DEVELOPMENT, 1998, 12 (12) : 1763 - 1768
  • [3] Pancreatic and duodenal homeobox 1 (PDX1) phosphorylation at serine-269 is HIPK2-dependent and affects PDX1 subnuclear localization
    An, Rong
    Xavier, Gabriela da Silva
    Semplici, Francesca
    Vakhshouri, Saharnaz
    Hao, Huai-Xiang
    Rutter, Jared
    Pagano, Mario A.
    Meggio, Flavio
    Pinna, Lorenzo A.
    Rutter, Guy A.
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 399 (02) : 155 - 161
  • [4] Molecular diagnosis of maturity-onset diabetes of the young (MODY) in Turkish children by using targeted next-generation sequencing
    Anik, Ahmet
    Catli, Gonul
    Abaci, Ayhan
    Sari, Erkan
    Yesilkaya, Ediz
    Korkmaz, Huseyin Anil
    Demir, Korcan
    Altincik, Ayca
    Tuhan, Hale Unver
    Kizildag, Sefa
    Ozkan, Behzat
    Ceylaner, Serdar
    Bober, Ece
    [J]. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2015, 28 (11-12) : 1265 - 1271
  • [5] [Anonymous], 1999, DEF DIAGN CLASS DIAB
  • [6] Precision Diagnosis of Maturity-Onset Diabetes of the Young with Next-Generation Sequencing: Findings from the MODY-IST Study in Adult Patients
    Aydogan, Hulya Yilmaz
    Gul, Nurdan
    Demirci, Deniz Kanca
    Mutlu, Ummu
    Gulfidan, Gizem
    Arga, Kazim Yalcin
    Ozder, Aclan
    Camli, Ahmet Adil
    Tutuncu, Yildiz
    Ozturk, Oguz
    Cacina, Canan
    Darendeliler, Feyza
    Poyrazoglu, Sukran
    Satman, Ilhan
    [J]. OMICS-A JOURNAL OF INTEGRATIVE BIOLOGY, 2022, 26 (04) : 218 - 235
  • [7] Spectrum of mutations in monogenic diabetes genes identified from high-throughput DNA sequencing of 6888 individuals
    Bansal, Vikas
    Gassenhuber, Johann
    Phillips, Tierney
    Oliveira, Glenn
    Harbaugh, Rebecca
    Villarasa, Nikki
    Topol, Eric J.
    Seufferlein, Thomas
    Boehm, Bernhard O.
    [J]. BMC MEDICINE, 2017, 15
  • [8] A review of maturity onset diabetes of the young (MODY) and challenges in the management of glucokinase-MODY
    Bishay, Ramy H.
    Greenfield, Jerry R.
    [J]. MEDICAL JOURNAL OF AUSTRALIA, 2016, 205 (10) : 480 - +
  • [9] PDX1-MODY and dorsal pancreatic agenesis: New phenotype of a rare disease
    Caetano, L. A.
    Santana, L. S.
    Costa-Riquetto, A. D.
    Lerario, A. M.
    Nery, M.
    Nogueira, G. F.
    Ortega, C. D.
    Rocha, M. S.
    Jorge, A. A. L.
    Teles, M. G.
    [J]. CLINICAL GENETICS, 2018, 93 (02) : 382 - 386
  • [10] Chen Chunming, 2004, Biomed Environ Sci, V17 Suppl, P1