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Gender aspects in Mild cognitive Impairment (MCI) to Alzheimer's Disease (AD) conversion. A Romanian epidemiological study.

机译:在轻度认知障碍(MCI)对阿尔茨海默病(AD)转换的性别方面。罗马尼亚流行病学研究。

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A particular matter in the mild cognitive impairment (MCI) to Alzheimer's disease (AD) conversion refers to the gender differences regarding the clinical phenotype, comorbidity and risk factors. Our study was fulfilled on 60 MCI subjects and assessed the risk factors and co-morbidity pre-valence in MCI patients de-pending on sex). Hypertension and dyslipidemia seem to be the main risk factors for MCI to AD progression. The sex-dependent comorbidity distribution is evident at baseline (except transient ischemic attack, all comorbidities prevailed in women). During 3 years follow up the women percent exhibiting hypertension, dyslipidemia, angina pectoris, transient ischemic attack, and diabetes type II significantly decreased, while those afflicted by osteoporosis and hypothyroidism increased. The lack of significant changes in the co-morbidities' of men, and the slight increased incidence of hypertension and transient ischemic attack in men need further clarification. Depression incidence is also sex dependent: 13% in women as against 3% in men at baseline, and increasing in the former from 13% to 20% during the follow up. No percent modification was registered in men. Depression needs to be differentiated from that of the subjects with depression-related cognitive impairment. The total amount of 23% patients with depression in our study could suggest that these subjects should not be excluded from the cohorts for preclinical Alzheimer studies.
机译:在轻度认知障碍(MCI)中,对阿尔茨海默病(AD)转化的特定物质是指有关临床表型,合并症和危险因素的性别差异。我们的研究符合60 MCI受试者,并评估了在性行为的MCI患者中的危险因素和共发病率预价)。高血压和血脂血症似乎是MCI对广告进展的主要风险因素。性依赖性合并症分布在基线(除了短暂的缺血性攻击之外,妇女普遍存在的所有合并症)是显而易见的。 3年内,随后患有高血压,血脂血症,心绞痛,短暂性缺血性发作和糖尿病II型患者的百分比显着下降,而骨质疏松症和甲状腺功能亢进的患者增加。男性的共同生命缺乏显着变化,以及男性的高血压发病率和瞬态缺血攻击的略微增加需要进一步澄清。抑郁发病率也是性依赖性:13%的女性在基线的男性中,在3%的男性中,在后续行动期间,前者增加了13%至20%。在男性中注册了任何修改百分比。抑郁症需要与抑郁相关的认知障碍的主体的抑郁症。我们研究中抑郁症患者的总量可以暗示这些受试者不应被排除在临床前阿尔茨海默研究的队列之外。

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