Genotype-Phenotype Relationship and Follow-up Analysis of a Chinese Cohort With Osteogenesis Imperfecta

被引:4
|
作者
Wei, Shuoshuo [1 ,2 ,3 ,4 ]
Yao, Yangyang [5 ,6 ]
Shu, Meng [1 ,2 ,3 ,4 ]
Gao, Ling [1 ,2 ,3 ,4 ]
Zhao, Jiajun [1 ,2 ,3 ,4 ]
Li, Tianyou [5 ,6 ]
Wang, Yanzhou [5 ,6 ,7 ]
Xu, Chao [1 ,2 ,3 ,4 ,8 ]
机构
[1] Shandong Univ, Shandong Prov Hosp, Cheeloo Coll Med, Dept Endocrinol & Metab, Jinan, Shandong, Peoples R China
[2] Shandong First Med Univ, Dept Endocrinol & Metab, Shandong Prov Hosp, Jinan, Peoples R China
[3] Shandong Acad Clin Med, Inst Endocrinol, Jinan, Shandong, Peoples R China
[4] Shandong Clin Med Ctr Endocrinol & Metab, Jinan, Shandong, Peoples R China
[5] Shandong Univ, Shandong Prov Hosp, Cheeloo Coll Med, Dept Pediat Orthoped, Jinan, Shandong, Peoples R China
[6] Shandong First Med Univ, Dept Pediat Orthoped, Shandong Prov Hosp, Jinan, Peoples R China
[7] Shandong Univ, Shandong Prov Hosp, Cheeloo Coll Med, Dept Pediat Orthoped, Jinan 250021, Shandong, Peoples R China
[8] Shandong Univ, Shandong Prov Hosp, Cheeloo Coll Med, Dept Endocrinol & Metab, Jinan 250021, Shandong, Peoples R China
关键词
osteogenesis imperfect; Chinese cohort; follow-up; genotype-phenotype relationship; treatment effect; BISPHOSPHONATE THERAPY; SEQUENCE VARIANTS; HELICAL DOMAIN; CHILDREN; MUTATION; PAMIDRONATE; ADOLESCENTS; PREVALENCE; MECHANISMS; SPECTRUM;
D O I
10.1016/j.eprac.2022.05.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To evaluate the genotype-phenotype relationship and the effect of treatment on the clinical course of osteogenesis imperfecta (OI).Methods: We established a Chinese hospitalized cohort with OI and followed them up for an average of 6 years. All patients were confirmed as having OI using whole-exome sequencing. We analyzed the genotype -phenotype relationship based on different types, pathogenic mechanisms, and gene inheritance patterns of OI. Additionally, we assessed whether there was a difference in treatment efficacy based on genotype.Results: One hundred sixteen mutations in 6 pathogenic genes (COL1A1, COL1A2, IFITM5, SERPINF1, FKBP10, and WNT1) were identified in 116 patients with type I, III, IV, V, VI, XI, or XV OI. Compared with patients with COL1A1 mutations, patients with COL1A2 mutations were younger at the time of the first fracture, whereas other phenotypes were similar. When 3 groups (helical, haploinsufficiency, and non -collagen I gene mutations) were compared, patients with helical mutations were the shortest and most prone to dentinogenesis imperfecta. Patients with haploinsufficiency mutations were the oldest at the time of the first fracture. Moreover, patients with non-collagen I gene mutations were least sus-ceptible to blue sclerae and had the highest fracture frequency. Furthermore, there were some minor phenotypic differences among non-collagen I gene mutations. Interestingly, pamidronate achieved excellent results in the treatment of patients with OI, and the treatment effect appeared to be unrelated to their genotypes.Conclusion: Our findings indicated a genotype-phenotype relationship and a similar effect of pamidro-nate treatment in patients with OI, which could provide a basis for guiding clinical treatment and pre-dicting OI prognosis.(c) 2022 AACE. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:760 / 766
页数:7
相关论文
共 50 条
  • [1] Longitudinal analysis of the audiological phenotype in osteogenesis imperfecta: a follow-up study
    Martens, S.
    Dhooge, I. J. M.
    Swinnen, F. K. R.
    JOURNAL OF LARYNGOLOGY AND OTOLOGY, 2018, 132 (08): : 703 - 710
  • [2] Diagnostic strategies and genotype-phenotype correlation in a large Indian cohort of osteogenesis imperfecta
    Mrosk, Julia
    Bhavani, Gandham SriLakshmi
    Shah, Hitesh
    Hecht, Jochen
    Kruger, Ulrike
    Shukla, Anju
    Kornak, Uwe
    Girisha, Katta Mohan
    BONE, 2018, 110 : 368 - 377
  • [3] Genotype-phenotype relationship and comparison between eastern and western patients with osteogenesis imperfecta
    Lin, X.
    Hu, J.
    Zhou, B.
    Zhang, Q.
    Jiang, Y.
    Wang, O.
    Xia, W.
    Xing, X.
    Li, M.
    JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2024, 47 (01) : 67 - 77
  • [4] Genotype-Phenotype Correlations in Autosomal Dominant Osteogenesis Imperfecta
    Ben Amor, I. Mouna
    Glorieux, Francis H.
    Rauch, Frank
    JOURNAL OF OSTEOPOROSIS, 2011, 2011
  • [5] Genotype-phenotype study in type V osteogenesis imperfecta
    Balasubramanian, Meena
    Parker, Michael J.
    Dalton, Ann
    Giunta, Cecilia
    Lindert, Uschi
    Peres, Luiz C.
    Wagner, Bart E.
    Arundel, Paul
    Offiah, Amaka
    Bishop, Nicholas J.
    CLINICAL DYSMORPHOLOGY, 2013, 22 (03) : 93 - 101
  • [6] Genotype-phenotype correlation among Malaysian patients with osteogenesis imperfecta
    Nawawi, Nadiah Mohd
    Selveindran, Nalini M.
    Rasat, Rahmah
    Ping, Chow Yock
    Latiff, Zarina Abdul
    Zakaria, Syed Zulkifli Syed
    Jamal, Rahman
    Murad, Nor Azian Abdul
    Abd Aziz, Bilkis Banu
    CLINICA CHIMICA ACTA, 2018, 484 : 141 - 147
  • [7] Genotype-phenotype correlations in 294 pediatric patients with osteogenesis imperfecta
    Byrd, Jay J.
    White, Andrew C.
    Nissen, Claire G.
    Schissel, Makayla
    Van Ormer, Matthew
    Velasco, Danita
    Wallace, Maegen
    JBMR PLUS, 2024, 8 (11)
  • [8] Phenotype and Genotype Analysis of Chinese Patients with Osteogenesis Imperfecta Type V
    Zhang, Zeng
    Li, Mei
    He, Jin-Wei
    Fu, Wen-Zhen
    Zhang, Chang-Qing
    Zhang, Zhen-Lin
    PLOS ONE, 2013, 8 (08):
  • [9] Genotype-phenotype analysis of a rare type of osteogenesis imperfecta in four Chinese families with WNT1 mutations
    Liu, Yi
    Song, Lijie
    Ma, Doudou
    Lv, Fang
    Xu, Xiaojie
    Wang, Jianyi
    Xia, Weibo
    Jiang, Yan
    Wang, Ou
    Song, Yuwen
    Xing, Xiaoping
    Asan
    Li, Mei
    CLINICA CHIMICA ACTA, 2016, 461 : 172 - 180
  • [10] Mutation spectrum, genotype-phenotype correlation & digenic inheritance in a large Indian cohort of osteogenesis imperfecta
    Bhavani, G. S.
    Mrosk, J.
    Shah, H.
    Hecht, J.
    Krueger, U.
    Shukla, A.
    Kornak, U.
    Girisha, K. M.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 121 - 121