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C 反应蛋白与痴呆家族风险:认知成功老化的表型。

C-reactive protein and familial risk for dementia: a phenotype for successful cognitive aging.

机构信息

Department of Psychiatry, Mount Sinai School of Medicine, New York, USA.

出版信息

Neurology. 2012 Sep 11;79(11):1116-23. doi: 10.1212/WNL.0b013e3182698c89. Epub 2012 Aug 15.

Abstract

OBJECTIVES

Identifying phenotypes for successful cognitive aging, intact cognition into late-old age (>age 75), can help identify genes and neurobiological systems that may lead to interventions against and prevention of late-life cognitive impairment. The association of C-reactive protein (CRP) with cognitive impairment and dementia, observed primarily in young-elderly samples, appears diminished or reversed in late-old age (75+ years). A family history study determined if high CRP levels in late-old aged cognitively intact probands are associated with a reduced risk of dementia in their first-degree family members, suggesting a familial successful cognitive aging phenotype.

METHODS

The primary sample was 1,329 parents and siblings of 277 cognitively intact male veteran probands at least 75 years old. The replication sample was 202 relatives of 51 cognitively intact community-ascertained probands at least 85 years old. Relatives were assessed for dementia by proband informant interview. Their hazard ratio (HR) for dementia as a function of the proband's log-transformed CRP was calculated using the proportional hazards model.

RESULTS

Covarying for key demographics, higher CRP in probands was strongly associated with lower risk of dementia in relatives (HR = 0.55 [95% confidence interval (CI) 0.41, 0.74], p < 0.02). The replication sample relationship was in the same direction, stronger in magnitude, and also significant (HR = 0.15 [95% CI 0.06, 0.37], p < 0.0001).

CONCLUSIONS

Relatives of successful cognitive aging individuals with high levels of CRP are relatively likely to remain free of dementia. High CRP in successful cognitive aging individuals may constitute a phenotype for familial-and thus possibly genetic-successful cognitive aging.

摘要

目的

识别成功认知老化的表型,即认知完整到老年后期(>75 岁),有助于确定可能导致干预和预防老年认知障碍的基因和神经生物学系统。C 反应蛋白(CRP)与认知障碍和痴呆的关联主要在年轻老年人样本中观察到,在老年后期(75 岁及以上)似乎减弱或逆转。一项家族史研究确定了在认知完整的高龄被试中 CRP 水平较高是否与一级亲属痴呆风险降低相关,这表明存在家族性成功认知老化表型。

方法

主要样本为 277 名认知完整的 75 岁以上男性退伍军人被试的 1329 名父母和兄弟姐妹。复制样本为 202 名认知完整的社区确定的 51 名 85 岁以上被试的亲属。通过被试知情者访谈评估亲属的痴呆情况。使用比例风险模型计算 CRP 对数转换的被试的风险比(HR)作为痴呆的函数。

结果

在协变量为关键人口统计学特征的情况下,被试的 CRP 水平较高与亲属痴呆风险降低呈强相关(HR=0.55[95%置信区间(CI)0.41,0.74],p<0.02)。复制样本的关系呈相同方向,强度更大,且也具有统计学意义(HR=0.15[95%CI 0.06,0.37],p<0.0001)。

结论

具有高水平 CRP 的成功认知老化个体的亲属更有可能保持无痴呆状态。成功认知老化个体的 CRP 水平较高可能构成家族性成功认知老化的表型,因此可能具有遗传相关性。

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