From the Department of Epidemiology, Graduate School of Public Health (A.L.R., C.R.), and Department of Psychiatry (H.J.A.), University of Pittsburgh, PA; Departments of Radiology and Neurology (N.I.B.), University of Michigan, Ann Arbor; Laboratory of Epidemiology and Population Sciences (L.J.L.), National Institute on Aging, Baltimore, MD; and Departments of Psychiatry, Neurology, and Epidemiology & Biostatistics (K.Y.), University of California, San Francisco.
Neurology. 2018 Jan 16;90(3):e223-e229. doi: 10.1212/WNL.0000000000004842. Epub 2017 Dec 15.
Mild parkinsonian signs (MPS) are an underappreciated neurologic condition in older adults; we assessed associations of MPS with measures of dopaminergic (catechol-O-methyltransferase [COMT] genotype, an indicator of synaptic dopamine levels) and vascular (white matter hyperintensities [WMH], an indicator of cerebral small vessel disease) factors.
In a cohort of older adults (mean age 82.6 years [SD 2.6]; 58.0% female; 38.8% black), we assessed cross-sectional associations of WMH volume and COMT Val158Met (rs4680) genotype (n = 35 Met/Met, n = 180 Val carriers) with MPS by regression models adjusted for demographic and health characteristics. Interactions between WMH and COMT were assessed and analyses were repeated stratified by COMT genotype (Met/Met related to higher synaptic dopamine vs Val carriers related to lower synaptic dopamine).
MPS was present in 42.3% of our sample. WMH (odds ratio [OR] 1.16, confidence interval [CI] 1.05-1.27) but not COMT (Met/Met compared to Val carrier: OR 0.62, CI 0.27-1.42) was related to MPS. There was a significant interaction between WMH and COMT ( = 0.03). Stratified analyses reveled a strong association between WMH and MPS among COMT Val carriers (OR 1.23, CI 1.09-1.38), but not for Met/Met (OR 0.68, CI 0.45-1.02), independent of covariates.
WMH had a direct relation with MPS. In contrast, COMT was not associated with MPS, but it did modify the effect of WMH on MPS. The dopaminergic system may provide compensation for the effects of WMH on MPS. These findings suggest that MPS has a vascular rather than dopaminergic origin in older adults, but both factors are important in MPS manifestation.
轻度帕金森体征(MPS)是老年人中一种未被充分认识的神经系统疾病;我们评估了 MPS 与多巴胺能(儿茶酚-O-甲基转移酶[COMT]基因型,突触多巴胺水平的指标)和血管(脑白质高信号[WMH],脑小血管疾病的指标)因素的关系。
在一项老年队列研究中(平均年龄 82.6 岁[标准差 2.6];58.0%为女性;38.8%为黑人),我们通过回归模型评估了 WMH 体积和 COMT Val158Met(rs4680)基因型(n = 35 Met/Met,n = 180 Val 携带者)与 MPS 的横断面相关性,这些模型调整了人口统计学和健康特征。评估了 WMH 和 COMT 之间的相互作用,并根据 COMT 基因型(Met/Met 与较高的突触多巴胺相关,而 Val 携带者与较低的突触多巴胺相关)对分析进行了分层。
我们样本中有 42.3%的人存在 MPS。WMH(比值比[OR] 1.16,置信区间[CI] 1.05-1.27)而不是 COMT(Met/Met 与 Val 携带者相比:OR 0.62,CI 0.27-1.42)与 MPS 相关。WMH 和 COMT 之间存在显著的相互作用( = 0.03)。分层分析显示,在 COMT Val 携带者中,WMH 与 MPS 之间存在强烈的关联(OR 1.23,CI 1.09-1.38),但在 Met/Met 中则没有(OR 0.68,CI 0.45-1.02),独立于协变量。
WMH 与 MPS 有直接关系。相比之下,COMT 与 MPS 无关,但它确实改变了 WMH 对 MPS 的影响。多巴胺能系统可能为 WMH 对 MPS 的影响提供补偿。这些发现表明,在老年人中,MPS 的发生具有血管源性而不是多巴胺能源性,但这两个因素在 MPS 的表现中都很重要。