Yang Shuman, Leslie William D, Yan Lin, Walld Randy, Roos Leslie L, Morin Suzanne N, Majumdar Sumit R, Lix Lisa M
Department of Internal Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
Department of Community Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
J Bone Miner Res. 2016 Sep;31(9):1753-9. doi: 10.1002/jbmr.2849. Epub 2016 Apr 30.
Parental hip fracture (HF) is considered a major risk factor for offspring major osteoporotic fracture (MOF), but all studies to date have relied on self-reported information of uncertain accuracy. We tested the association of objectively verified parental HF with offspring MOF and HF. We used a population-based historical cohort study of 261,705 offspring (age ≥40 years) with at least one linked parent (total 478,792 parents) for the province of Manitoba, Canada. Cox proportional hazards models were developed to test hazard ratio (HR) for offspring MOF and HF for 1997 to 2014 according to prior parental HF dating back to 1970. The median age of offspring at study entry was 40 years (range, 40 to 50 years), and 48.3% were women. During 2.9 million person-years of offspring follow-up (median per offspring, 12 years), we identified 7323 incident MOF (4.4% versus 2.7% for those with and without a parental HF, p < 0.001), including 331 HF (0.3% versus 0.1%, p < 0.001). Parental HF was independently associated with increased risk of offspring MOF (HR, 1.30; 95% confidence interval [CI], 1.20 to 1.41). The strength of the association decreased with older parental age at HF (ptrend < 0.001), and was no longer significant if parental HF occurred after age 80 years (adjusted HR, 1.07; 95% CI, 0.96 to 1.19). The relationship between parental HF and offspring HF was even stronger than for MOF (adjusted HR, 1.64; 95% CI, 1.21 to 2.23). Associations with MOF or HF were not affected by either the gender of the parent with HF or the gender of the offspring. Parental HF increased the risk for offspring MOF and HF but not when parental HF occurred after age 80 years. This suggests a more nuanced approach for clinicians trying to stratify fracture risk, and illustrates the enormous potential of parent-offspring record linkage for other familial disorders. © 2016 American Society for Bone and Mineral Research.
父母髋部骨折(HF)被认为是后代发生严重骨质疏松性骨折(MOF)的主要危险因素,但迄今为止所有研究都依赖于准确性存疑的自我报告信息。我们检验了经客观证实的父母HF与后代MOF及HF之间的关联。我们对加拿大曼尼托巴省261,705名后代(年龄≥40岁)及至少一位有记录关联的父母(共478,792名父母)进行了一项基于人群的历史性队列研究。构建Cox比例风险模型,以根据可追溯至1970年的父母既往HF情况,检验1997年至2014年后代MOF及HF的风险比(HR)。研究纳入时后代的中位年龄为40岁(范围40至50岁),女性占48.3%。在对后代进行的290万人年的随访期间(每位后代的中位随访时间为12年),我们确定了7323例新发MOF(父母有HF者为4.4%,无父母HF者为2.7%,p<0.001),其中包括331例HF(父母有HF者为0.3%,无父母HF者为0.1%,p<0.001)。父母HF与后代MOF风险增加独立相关(HR为1.30;95%置信区间[CI]为1.20至1.41)。关联强度随父母发生HF时年龄增大而降低(p趋势<0.001),如果父母HF发生在80岁以后则不再具有显著性(校正后HR为1.07;95%CI为0.96至1.19)。父母HF与后代HF之间的关系甚至比与MOF之间的关系更强(校正后HR为1.64;95%CI为1.21至2.23)。与MOF或HF的关联不受有HF父母的性别或后代性别的影响。父母HF会增加后代MOF和HF的风险,但父母HF发生在8