Cohen Jesse S, Radhakrishnan Hamsanandini, Olm Christopher A, Das Sandhitsu R, Cook Philip A, Wolk David A, Weintraub Daniel, Irwin David J, McMillan Corey T
medRxiv. 2024 Aug 16:2024.08.16.24312102. doi: 10.1101/2024.08.16.24312102.
Excessive daytime sleepiness (EDS) is a disabling symptom of Lewy body disorders (LBD). The hypothalamus is a key sleep-wake regulator, but its contribution to EDS in LBD remains unclear.
Use diffusion MRI to evaluate the relationship of hypothalamic microstructure to EDS symptoms in LBD.
We studied 102 patients with clinically-defined LBD (Parkinson's disease, n=93; Parkinson's disease dementia, n=4; and dementia with Lewy bodies, n=5) and Epworth Sleepiness Scale (ESS) within 2 years of MRI. Mean diffusivity (MD) was compared between EDS+ (ESS≥10, n=37) and EDS- (ESS<10, n=65) groups in the whole hypothalamus and three subregions, covarying for age and sex. Secondary analyses tested correlations between subregion MD and continuous ESS, global cognition, and motor scores; and between subregion volume and continuous ESS.
MD was increased in EDS+ compared to EDS- only in the inferior tuberal subregion (Cohen's d=0.43, p=0.043, β=0.117±0.057), with trend level differences in the whole hypothalamus (Cohen's d=0.39, p=0.064, β=0.070±0.037) and superior tuberal subregion (Cohen's d=0.38, p=0.073, β=0.063±0.035). No difference was seen in the posterior subregion (Cohen's d=0.1, p=0.628, β=0.019±0.038). Significant correlations with continuous ESS were seen in MD of whole hypothalamus (r=0.074, p=0.0057), superior tuberal (r=0.081, p=0.0038), and inferior tuberal (r=0.073, p=0.0059) subregions. There was no correlation of hypothalamic MD with global cognition or motor scores, and no correlation of whole/subregional hypothalamic volumes with ESS.
Daytime sleepiness associates with increased MD in the inferior tuberal hypothalamus in an LBD cohort. This suggests degeneration within this region could contribute to EDS symptoms.
日间过度嗜睡(EDS)是路易体障碍(LBD)的一种致残症状。下丘脑是睡眠-觉醒的关键调节中枢,但其在LBD的EDS中的作用尚不清楚。
使用扩散磁共振成像(MRI)评估下丘脑微观结构与LBD中EDS症状的关系。
我们研究了102例临床确诊的LBD患者(帕金森病,n = 93;帕金森病痴呆,n = 4;路易体痴呆,n = 5),并在MRI检查后2年内进行了爱泼华嗜睡量表(ESS)评估。比较了EDS+组(ESS≥10,n = 37)和EDS-组(ESS<10,n = 65)在整个下丘脑及三个亚区域的平均扩散率(MD),并对年龄和性别进行了协变量调整。二次分析测试了亚区域MD与连续ESS、整体认知和运动评分之间的相关性;以及亚区域体积与连续ESS之间的相关性。
与EDS-组相比,EDS+组仅在下丘脑结节下亚区域的MD增加(Cohen's d = 0.43,p = 0.043,β = 0.117±0.057),在整个下丘脑(Cohen's d = 0.39,p = 0.064,β = 0.070±0.037)和结节上亚区域(Cohen's d = 0.38,p = 0.073,β = 0.063±0.035)有趋势性差异。在后亚区域未见差异(Cohen's d = 0.1,p = 0.628,β = 0.019±(此处原文有误,应为0.038)0.038)。在整个下丘脑(r = 0.074,p = 0.0057)、结节上(r = 0.081,p = 0.0038)和结节下(r = 0.073,p = 0.0059)亚区域的MD与连续ESS之间存在显著相关性。下丘脑MD与整体认知或运动评分无相关性,下丘脑整体/亚区域体积与ESS也无相关性。
在LBD队列中,日间嗜睡与下丘脑结节下亚区域MD增加相关。这表明该区域的退变可能导致EDS症状。