Fanfan Zheng, School of Nursing, Peking Union Medical College, Chinese Academy of Medical Sciences, 33 Ba Da Chu Road, Shijingshan District, 100144, Beijing, China; E-mail:
J Prev Alzheimers Dis. 2024;11(4):1132-1139. doi: 10.14283/jpad.2024.56.
A history of fracture has been associated with increased risk of dementia; however, it is uncertain whether sex difference exists in the association between prior fracture and subsequent risk of incident dementia.
To investigate whether sex modified the relationship between prior fracture and subsequent risk of dementia.
Prospective cohort study.
UK Biobank.
496,331 participants (54.6% women) free of dementia at baseline.
History of fracture was self-reported via touchscreen questionnaires at baseline. The primary outcome was all-cause dementia.
Both any fracture and fragility fracture were significantly associated with an increased risk of subsequent all-cause dementia in men (adjusted hazard ratio (HR): 1.28; 95% confidence interval (CI): 1.14-1.43; adjusted HR: 1.48; 95% CI: 1.18-1.87, respectively), but not in women (adjusted HR: 1.04; 95% CI 0.95-1.15; adjusted HR: 1.01; 95% CI: 0.87-1.18, respectively); and these sex-differences were significant (P interaction = 0.006; P interaction = 0.007, respectively). The sex differences in the impacts of different fracture sites (including upper limb, lower limb, spine, and multiple sites) were consistent on all-cause dementia.
This study demonstrated that prior fracture was associated with an increased risk of dementia in men but not in women, and the sex difference was significant. Previous fracture may be an important marker for identifying subsequent dementia in middle-aged and older men.
骨折史与痴呆风险增加相关;然而,骨折与随后痴呆风险之间的关联是否存在性别差异尚不确定。
研究既往骨折与随后痴呆风险之间的关系是否存在性别差异。
前瞻性队列研究。
英国生物银行。
496331 名基线时无痴呆的参与者(54.6%为女性)。
骨折史通过基线时的触摸屏问卷进行自我报告。主要结局为全因痴呆。
男性任何骨折和脆性骨折均与随后发生全因痴呆的风险增加显著相关(调整后的危险比(HR):1.28;95%置信区间(CI):1.14-1.43;调整后的 HR:1.48;95% CI:1.18-1.87),但在女性中则不然(调整后的 HR:1.04;95% CI:0.95-1.15;调整后的 HR:1.01;95% CI:0.87-1.18);且这些性别差异具有统计学意义(P 交互=0.006;P 交互=0.007)。不同骨折部位(包括上肢、下肢、脊柱和多处)对全因痴呆的影响在性别间差异一致。
本研究表明,既往骨折与男性而非女性的痴呆风险增加相关,且性别差异具有统计学意义。既往骨折可能是识别中老年男性后续痴呆的一个重要标志物。