Department of Internal Medicine, Section Endocrinology, Amsterdam Rare Bone Disease/Amsterdam Bone Center, Amsterdam University Medical Center, location VUmc, Amsterdam, Netherlands.
Department of Human Genetics, Amsterdam Movement Sciences, Amsterdam Rare Bone Disease/Amsterdam Bone Center, Amsterdam University Medical Center, location VUmc, Amsterdam, Netherlands.
Front Endocrinol (Lausanne). 2022 Apr 25;13:869604. doi: 10.3389/fendo.2022.869604. eCollection 2022.
Osteogenesis Imperfecta (OI) is a complex disease caused by genetic alterations in production of collagen type I, and collagen-related proteins. Bone fragility is the most common patient issue, but extraskeletal complications also present an adverse factor in the quality of life and prognosis of patients with OI. However, still little is known about the morbidity and mortality of these patients. The objective of this paper is to determine and describe to what extent OI impacts patients' life in terms of hospitalization and complications describing the incidence and prevalence of the Dutch cohort of OI patients and the characteristics of their hospital admissions. Information regarding OI patients and their hospital admission was extracted from the Statistics Netherlands Database and matched to the OI Genetics Database of Amsterdam UMC. Hospital admission data was available for 674 OI patients. This OI nationwide registry study shows that the life expectancy of OI patients is adversely affected by the disease. The median annual incidence risk of OI between 1992 and 2019 was 6.5 per 100,000 live births. Furthermore, patients with OI had a 2.9 times higher hospitalization rate compared to the general Dutch population. The highest hospitalization rate ratio of 8.4 was reported in the patient group between 0 and 19 years old. OI type and severity had impact on extraskeletal manifestations, which play a key role in the numerous hospital admissions. More awareness about the impact of OI on patients' life is needed to improve and implement prevention and follow-up guidelines.
成骨不全症(OI)是一种由 I 型胶原和胶原相关蛋白产生的遗传改变引起的复杂疾病。骨骼脆弱是最常见的患者问题,但骨骼外并发症也对 OI 患者的生活质量和预后产生不利影响。然而,人们对这些患者的发病率和死亡率仍然知之甚少。本文的目的是确定并描述 OI 在多大程度上影响患者的生活,包括住院和并发症,描述荷兰 OI 患者队列的发病率和患病率,以及他们住院的特点。OI 患者及其住院信息是从荷兰统计局数据库中提取的,并与阿姆斯特丹 UMC 的 OI 遗传学数据库相匹配。共有 674 名 OI 患者的住院数据可用。这项全国性 OI 登记研究表明,OI 患者的预期寿命受到该疾病的不利影响。1992 年至 2019 年期间,OI 的年平均发病率风险为每 10 万活产儿 6.5 例。此外,OI 患者的住院率比荷兰普通人群高 2.9 倍。在 0 至 19 岁的患者组中,报告的住院率比值最高,为 8.4。OI 类型和严重程度对骨骼外表现有影响,骨骼外表现在多次住院中起着关键作用。需要更多地了解 OI 对患者生活的影响,以改善和实施预防和随访指南。