Is Osteogenesis Imperfecta Associated with Cardiovascular Abnormalities? A Systematic Review of the Literature

被引:0
|
作者
Sara J. E. Verdonk
Silvia Storoni
Dimitra Micha
Joost G. van den Aardweg
Paolo Versacci
Luca Celli
Ralph de Vries
Lidiia Zhytnik
Otto Kamp
Marianna Bugiani
Elisabeth M. W. Eekhoff
机构
[1] Amsterdam UMC Location Vrije Universiteit,Department of Endocrinology and Metabolism
[2] Rare Bone Disease Center,Department of Human Genetics
[3] Amsterdam Movement Sciences,Department of Respiratory Medicine
[4] Amsterdam UMC Location Vrije Universiteit,Department of Maternal Infantile and Urological Sciences
[5] Amsterdam Reproduction and Development,Medical Library
[6] Amsterdam University Medical Center,Department of Traumatology and Orthopeadics
[7] Location AMC,Department of Cardiology
[8] Sapienza University of Rome,Department of Pathology
[9] Vrije Universiteit,undefined
[10] University of Tartu,undefined
[11] Amsterdam UMC Location Vrije Universiteit,undefined
[12] Amsterdam UMC Location AMC,undefined
来源
Calcified Tissue International | 2024年 / 114卷
关键词
Osteogenesis imperfecta; Collagen type I; Cardiovascular disease; Aortic root dilatation;
D O I
暂无
中图分类号
学科分类号
摘要
Osteogenesis imperfecta (OI) is a rare genetic disorder caused by abnormal collagen type I production. While OI is primarily characterized by bone fragility and deformities, patients also have extraskeletal manifestations, including an increased risk of cardiovascular disease. This review provides a comprehensive overview of the literature on cardiovascular diseases in OI patients in order to raise awareness of this understudied clinical aspect of OI and support clinical guidelines. In accordance with the PRISMA guidelines, a systematic literature search in PubMed, Embase, Web of Science and Scopus was conducted that included articles from the inception of these databases to April 2023. Valvular disease, heart failure, atrial fibrillation, and hypertension appear to be more prevalent in OI than in control individuals. Moreover, a larger aortic root was observed in OI compared to controls. Various cardiovascular diseases appear to be more prevalent in OI than in controls. These cardiovascular abnormalities are observed in all types of OI and at all ages, including young children. As there are insufficient longitudinal studies, it is unknown whether these abnormalities are progressive in nature in OI patients. Based on these findings, we would recommend referring individuals with OI to a cardiologist with a low-threshold.
引用
收藏
页码:210 / 221
页数:11
相关论文
共 50 条
  • [41] Systematic review of health related-quality of life in adults with osteogenesis imperfecta
    Darran Mc Donald
    Tara Mc Donnell
    Julie Martin-Grace
    Gerry Mc Manus
    Rachel K. Crowley
    Orphanet Journal of Rare Diseases, 18
  • [42] Osteogenesis imperfecta: Review of 40 patients
    Caudevilla Lafuente, Pilar
    de Arriba Munoz, Antonio
    Izquierdo Alvarez, Silvia
    Ferrer Lozano, Marta
    Medrano San Ildefonso, Marta
    Labarta Aizpun, Jose Ignacio
    MEDICINA CLINICA, 2020, 154 (12): : 512 - 518
  • [43] Effect of Bisphosphonates on Function and Mobility Among Children With Osteogenesis Imperfecta: A Systematic Review
    Constantino, Christopher S.
    Krzak, Joseph J.
    Fial, Alissa, V
    Kruger, Karen M.
    Rammer, Jacob R.
    Radmanovic, Katarina
    Smith, Peter A.
    Harris, Gerald F.
    JBMR PLUS, 2019, 3 (10)
  • [44] Exploring the impact of Osteogenesis Imperfecta on families: A mixed-methods systematic review
    Hill, Melissa
    Lewis, Celine
    Riddington, Megan
    Crowe, Belinda
    DeVile, Catherine
    Gotherstrom, Cecilia
    Chitty, Lyn
    DISABILITY AND HEALTH JOURNAL, 2019, 12 (03) : 340 - 349
  • [45] Spine Pathologies in Osteogenesis Imperfecta: A Review
    Shchurova, Elena N.
    Ryabykh, Sergey O.
    Ochirova, Polina, V
    Popkov, Dmitry A.
    Ryabykh, Tatyana, V
    TRAVMATOLOGIYA I ORTOPEDIYA ROSSII, 2022, 28 (01): : 118 - 127
  • [46] Systematic review of health related-quality of life in adults with osteogenesis imperfecta
    Mc Donald, Darran
    Mc Donnell, Tara
    Martin-Grace, Julie
    Mc Manus, Gerry
    Crowley, Rachel K. K.
    ORPHANET JOURNAL OF RARE DISEASES, 2023, 18 (01)
  • [47] The patient clinical journey and socioeconomic impact of osteogenesis imperfecta: a systematic scoping review
    Maria Rapoport
    Michael B. Bober
    Cathleen Raggio
    Lena Lande Wekre
    Frank Rauch
    Ingunn Westerheim
    Tracy Hart
    Taco van Welzenis
    Arun Mistry
    James Clancy
    Lucy Booth
    Samantha Prince
    Oliver Semler
    Orphanet Journal of Rare Diseases, 18
  • [48] Dental manifestations of osteogenesis imperfecta and abnormalities of collagen I metabolism
    Lund, AM
    Jensen, BL
    Nielsen, LA
    Skovby, F
    JOURNAL OF CRANIOFACIAL GENETICS AND DEVELOPMENTAL BIOLOGY, 1998, 18 (01): : 30 - 37
  • [49] Echocardiographic abnormalities and joint hypermobility in Chinese patients with Osteogenesis imperfecta
    Yazhao Mei
    Yunyi Jiang
    Li Shen
    Zheying Meng
    Zhenlin Zhang
    Hao Zhang
    Orphanet Journal of Rare Diseases, 19
  • [50] Pseudoarthrosis of the Distal Humerus in Pediatric Osteogenesis Imperfecta Patients: A Case Series and Literature Review
    Laor, Boaz
    Addab, Sofia
    Janelle, Chantal
    Hamdy, Reggie C.
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (04)