THERAPY OF ENDOCRINE DISEASE Treatment of osteogenesis imperfecta in adults

被引:29
|
作者
Lindahl, Katarina [1 ]
Langdahl, Bente [2 ]
Ljunggren, Osten [1 ]
Kindmark, Andreas [1 ,3 ]
机构
[1] Univ Uppsala Hosp, Dept Med Sci, SE-75185 Uppsala, Sweden
[2] Aarhus Univ Hosp, Dept Endocrinol & Internal Med THG, DK-8000 Aarhus C, Denmark
[3] Univ Uppsala Hosp, Dept Med Sci, Sci Life Lab, SE-75185 Uppsala, Sweden
关键词
INTRAVENOUS PAMIDRONATE TREATMENT; EHLERS-DANLOS-SYNDROME; BONE-MINERAL DENSITY; BIRTH PREVALENCE RATES; I COLLAGEN; STEM-CELLS; BISPHOSPHONATE TREATMENT; PHENOTYPIC VARIABILITY; TERIPARATIDE TREATMENT; RNA INTERFERENCE;
D O I
10.1530/EJE-14-0017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Osteogenesis imperfecta (OI) is a heterogeneous rare connective tissue disorder commonly caused by mutations in the collagen type I genes. Pharmacological treatment has been most extensively studied in children, and there are only few studies comprising adult OI patients. Objectives: i) To review the literature on the current medical management of OI in children and adults, and thereby identify unmet medical needs and ii) to present an overview of possible future treatment options. Results: Individualization and optimization of OI treatment in adults remain a challenge, because available treatments do not target the underlying collagen defect, and available literature gives weak support for treatment decisions for adult patients. Conclusions: Bisphosphonates are still the most widely used pharmacological treatment for adult OI, but the current evidence supporting this is sparse and investigations on indications for choice and duration of treatment are needed.
引用
收藏
页码:R79 / R90
页数:12
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