Age and sex-specific risk in fractures with Down syndrome in a retrospective case-control study from Germany.

IF 2.1 2区 医学 Q1 EDUCATION, SPECIAL Journal of Intellectual Disability Research Pub Date : 2024-08-25 DOI:10.1111/jir.13183
S Krieg, A Krieg, K Kostev
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Abstract

Background: The increasing life expectancy of individuals with Down syndrome has led to a growing awareness of mid- and late-life conditions.

Methods: Based on the Disease Analyser database (IQVIA), this retrospective cohort study compared adults ≥18 years of age with Down syndrome (ICD-10: Q90) in general practices in Germany with a propensity score-matched cohort without Down syndrome. The outcome was the first diagnosis of a fracture within 5 years of the index date. The cumulative incidence of fractures over a 5-year period was presented using Kaplan-Meier curves. Univariable Cox regression analyses by age group and sex were performed to assess the association between Down syndrome and fractures.

Results: A total of 2547 individuals with Down syndrome and 12 735 individuals without Down syndrome were included in the study. A significantly higher cumulative fracture incidence within 5 years was observed in the age group 51-60 years (9.3% Down syndrome vs. 4.8% without Down syndrome, P = 0.003) as well as in the age group >60 years (20.3% Down syndrome vs. 8.6% without Down syndrome, P < 0.001) compared with the cohort without Down syndrome. Regression analysis showed a significant association between Down syndrome and fracture risk in women with Down syndrome aged 51-60 years (hazard ratio [HR] = 1.60; 95% confidence interval [CI]: 1.13-2.26), and in those aged 51-60 years (HR = 2.08; 95% CI: 1.27-3.41) and >60 years (HR = 2.98; 95% CI: 1.87-4.73)), but not in men. When comparing fractures in individuals with and without Down syndrome, shoulder and arm fractures were most common in the Down syndrome cohort.

Conclusion: The results of our study indicate a positive association between individuals with Down syndrome and subsequent fractures in women and those aged >50 years. Prevention of falls appears to be particularly important in these populations. However, future studies should clarify the extent to which socio-economic factors, such as housing, play a role in this context.

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德国一项回顾性病例对照研究中唐氏综合征患者骨折的年龄和性别风险。
背景:随着唐氏综合征患者预期寿命的延长,他们对中年和晚年状况的认识也在不断提高:随着唐氏综合征患者预期寿命的延长,人们对中晚期疾病的认识也在不断提高:这项回顾性队列研究以 Disease Analyser 数据库(IQVIA)为基础,比较了德国全科医生中年龄≥18 岁的唐氏综合征成人(ICD-10:Q90)与无唐氏综合征的倾向得分匹配队列。研究结果是在索引日期后的 5 年内首次诊断出骨折。5 年内骨折的累积发生率采用 Kaplan-Meier 曲线表示。按年龄组和性别进行单变量 Cox 回归分析,以评估唐氏综合征与骨折之间的关系:研究共纳入了 2547 名唐氏综合征患者和 12 735 名非唐氏综合征患者。在 51-60 岁年龄组(9.3% 的唐氏综合征患者与 4.8% 的非唐氏综合征患者,P = 0.003)和大于 60 岁年龄组(20.3% 的唐氏综合征患者与 8.6% 的非唐氏综合征患者,P 60 岁(HR = 2.98;95% CI:1.87-4.73))中观察到,5 年内累积骨折发生率明显较高,但在男性中没有观察到。在比较有唐氏综合征和无唐氏综合征患者的骨折情况时,肩部和手臂骨折在唐氏综合征人群中最为常见:结论:我们的研究结果表明,患有唐氏综合症的人与女性和年龄大于 50 岁的人随后发生骨折之间存在正相关。在这些人群中,预防跌倒似乎尤为重要。不过,未来的研究应明确住房等社会经济因素在这方面的作用。
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来源期刊
CiteScore
5.60
自引率
5.60%
发文量
81
期刊介绍: The Journal of Intellectual Disability Research is devoted exclusively to the scientific study of intellectual disability and publishes papers reporting original observations in this field. The subject matter is broad and includes, but is not restricted to, findings from biological, educational, genetic, medical, psychiatric, psychological and sociological studies, and ethical, philosophical, and legal contributions that increase knowledge on the treatment and prevention of intellectual disability and of associated impairments and disabilities, and/or inform public policy and practice. Expert reviews on themes in which recent research has produced notable advances will be included. Such reviews will normally be by invitation.
期刊最新文献
The influence of assistance in home-based exercise programmes for individuals with intellectual disabilities. The risk of type 2-diabetes among persons with intellectual disability: a Danish population-based matched cohort study. Issue Information Sleep problems of children with Down syndrome in northern China. 'It's especially good just to know that you're not the only one': a qualitative study exploring experiences with online peer support programmes for the Fragile X community.
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