George Mason University, School of Systems Biology, Manassas, VA, 22030, USA.
Neurocombinatorix, 5902 Mount Eagle Dr, Suite 1103, Alexandria, VA, 22303, USA.
Sci Rep. 2019 Dec 9;9(1):18639. doi: 10.1038/s41598-019-54867-8.
In absence of therapies targeting symptomatic dementia, better understanding of the biology underlying a cognitive decline is warranted. Here we present the results of a meta-analysis of the impact of osteoarthritis (OA) on cognitive decline and overall mortality. Across 7 independent datasets obtained in studies of populations in the USA, EU and Australia (NBER, NSHAP, TILDA, NACC, Kaiser Permanente, GRIM BOOKS, OAI, with a total of >7 × 10 profiles), OA cohorts demonstrated higher cognitive scores, later dementia onset as well as longer lifespan and lower age-specific all-cause mortality. Moreover, generalized OA with multiple localizations is associated with more significant reduction of mortality and dementia than a singly localized OA or no arthritis. In OA patients with younger ages, all-cause mortality was disproportionally reduced as compared to that in controls, while exponential term of Gompert'z hazard function was increased, accelerating mortality accrual at later ages. Up to 8-10% of poly-osteoarthritic patients are predicted and observed to reach centenarian lifespan, while in matched non-OA population the same benchmark is reached by less than 1% of patients. These results point at a possibility of life-extending and cognition preserving impacts of OA-conditioned immune system.
在缺乏针对症状性痴呆症的治疗方法的情况下,更好地了解认知能力下降的生物学基础是有必要的。在这里,我们对骨关节炎(OA)对认知能力下降和总体死亡率的影响进行了荟萃分析。这项研究分析了来自美国、欧盟和澳大利亚的 7 项独立人群研究数据集(NBER、NSHAP、TILDA、NACC、Kaiser Permanente、GRIM BOOKS、OAI,共有 >7×10 个档案),结果表明 OA 队列的认知评分更高,痴呆症发病时间更晚,寿命更长,特定年龄的全因死亡率更低。此外,与单部位 OA 或无关节炎相比,多部位 OA 与死亡率和痴呆症的显著降低更为相关。在年龄较小的 OA 患者中,与对照组相比,全因死亡率不成比例地降低,而 Gompertz 危险函数的指数项增加,加速了晚年的死亡率累积。多达 8-10%的多骨性关节炎患者预计和观察到达到百岁寿命,而在匹配的非 OA 人群中,不到 1%的患者达到这一基准。这些结果表明,OA 引起的免疫系统可能具有延长寿命和保护认知的作用。