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Microstructural changes in the inferior tuberal hypothalamus correlate with daytime sleepiness in Lewy body disease

Cohen, J. S.; Radhakrishnan, H.; Olm, C. A.; Das, S. R.; Cook, P. A.; Wolk, D. A.; Weintraub, D. A.; Irwin, D. J.; McMillan, C.

2024-08-16 neurology
10.1101/2024.08.16.24312102 medRxiv
Show abstract

BackgroundExcessive 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. ObjectivesUse diffusion MRI to evaluate the relationship of hypothalamic microstructure to EDS symptoms in LBD. MethodsWe studied 102 patients with clinically-defined LBD (Parkinsons disease, n=93; Parkinsons 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[&ge;]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. ResultsMD was increased in EDS+ compared to EDS-only in the inferior tuberal subregion (Cohens d=0.43, p=0.043, {beta}=0.117{+/-}0.057), with trend level differences in the whole hypothalamus (Cohens d=0.39, p=0.064, {beta}=0.070{+/-}0.037) and superior tuberal subregion (Cohens d=0.38, p=0.073, {beta}=0.063{+/-}0.035). No difference was seen in the posterior subregion (Cohens d=0.1, p=0.628, {beta}=0.019{+/-}0.038). Significant correlations with continuous ESS were seen in MD of whole hypothalamus (r2=0.074, p=0.0057), superior tuberal (r2=0.081, p=0.0038), and inferior tuberal (r2=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. ConclusionsDaytime 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.

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