Sex-specific progression of Parkinson's disease: A longitudinal mixed-models analysis

冷漠 帕金森病 蒙特利尔认知评估 心理学 医学 队列 物理疗法 疾病 内科学 痴呆
作者
Anne-Marie Hanff,Christopher McCrum,Armin Rauschenberger,Gloria Aguayo,Claire Pauly,Sonja R. Jónsdóttir,Olena Tsurkalenko,Maurice P. Zeegers,Anja Leist,Rejko Krueger
出处
期刊:Journal of Parkinson's disease [IOS Press]
卷期号:15 (4): 805-818 被引量:1
标识
DOI:10.1177/1877718x251339201
摘要

Background Despite its relevance, the clinical progression of motor- and non-motor symptoms associated with Parkinson's disease (PD) is poorly described and understood, particularly in relation to sex-specific differences in clinical progression. Objective Identification of differential aspects in disease progression in men and women with PD. Methods Linear mixed-model analyses of 802 people with typical PD from the Luxembourg Parkinson's study's prospective cohort (median time of follow-up = three years). We estimated the effect of time and its moderation by sex (alpha ≤ 0.05), including confidence intervals, for the following outcomes: MDS-UPDRS I-IV, Starkstein Apathy Scale, Beck Depression Inventory, Montreal Cognitive Assessment (MoCA), Sniffin’ sticks, bodily discomfort, rapid eye movement sleep behavior disorder questionnaire, PD Sleep Scale (PDSS), Munich Dysphagia Test-PD, Functional Mobility Composite Score, and the MDS-based tremor and postural instability and gait disturbances scale. In addition, the marginal means illustrated the symptoms’ trajectories in men and women. Men and women had similar age. Results Overall, we observed a slower progression (interaction effect) in women compared to men, especially for MoCA (−0.159, 95%CI [−0.272, −0.046], p = 0.006), PDSS (−0.716, 95%CI [−1.229, −0.203], p = 0.006), PIGD (0.133, 95%CI [0.025 0.241], p = 0.016), and MDS-UPDRS II (0.346, 95%CI [0.120, 0.572], p = 0.003). The finding for MDS-UPDRS II was significant (FWER of 5%) after adjustment for multiple comparisons (Bonferroni-Holm). Conclusions Next to the further exploration of sex-specific progression, interventions, proactive monitoring and communication strategies tailored to the symptoms progression and needs of men and women need to be developed.
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