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Neurocognitive Disorders and Dehydration in Older Patients: Clinical Experience Supports the Hydromolecular Hypothesis of Dementia

机译:老年患者的神经认知障碍和脱水:临床经验支持痴呆症的含水分子假设

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摘要

Abnormalities of water homeostasis can be early expressions of neuronal dysfunction, brain atrophy, chronic cerebrovasculopathy and neurodegenerative disease. The aim of this study was to analyze the serum osmolality of subjects with cognitive impairment. One thousand and ninety-one consecutive patients attending the Alzheimer’s Evaluation Unit were evaluated with the Mini-Mental State Examination (MMSE), 21-Item Hamilton Depression Rating Scale (HDRS-21), Activities of Daily Living (ADL), Instrumental-ADL (IADL), Mini Nutritional Assessment (MNA), Exton-Smith Scale (ESS), and Cumulative Illness Rating Scale (CIRS). For each patient, the equation for serum osmolality developed by Khajuria and Krahn was applied. Five hundred and seventy-one patients had cognitive decline and/or depression mood (CD-DM) and 520 did not have CD-DM (control group). Patients with CD-DM were less likely to be male (p < 0.001), and were more likely to be older (p < 0.001), have a significant clear cognitive impairment (MMSE: p < 0.001), show the presence of a depressive mood (HDRS-21: p < 0.001) and have major impairments in ADL (p < 0.001), IADL (p < 0.001), MNA (p < 0.001), and ESS (p < 0.001), compared to the control group. CD-DM patients had a higher electrolyte concentration (Na+: p < 0.001; K+: p < 0.001; Cl−: p < 0.001), risk of dehydration (osmolality p < 0.001), and kidney damage (eGFR: p = 0.021), than the control group. Alzheimer’s disease (AD) patients showed a major risk for current dehydration (p ≤ 0.001), and dehydration was associated with the risk of developing a type of dementia, like AD or vascular dementia (VaD) (OR = 2.016, p < 0.001). In the multivariate analysis, the presence of dehydration state was associated with ADL (p < 0.001) and IADL (p < 0.001), but independently associated with age (r2 = 0.0046, p = 0.77), ESS (r2 = 0.0052, p = 0.54) and MNA (r2 = 0.0004, p = 0.48). Moreover, younger patients with dementia were significantly more dehydrated than patients without dementia (65–75 years, p = 0.001; 76–85 years, p = 0.001; ≥86 years, p = 0.293). The hydromolecular hypothesis intends to explain the relationship between dehydration and cognitive impairment in older patients as the result of protein misfolding and aggregation, in the presence of a low interstitial fluid volume, which is a defect of the microcirculation. Defective proteins were shown to impair the amount of information in brain biomolecular mechanisms, with consequent neuronal and synaptic damage.
机译:水位稳态的异常可能是神经元功能障碍,脑萎缩,慢性脑梗死和神经变性疾病的早期表达。本研究的目的是分析具有认知障碍的受试者的血清渗透压。通过迷你精神状态检查(MMSE),21项Hamilton抑郁率(HDRS-21),日常生活(ADL),仪器 - ADL的活动评估了参加阿尔茨海默氏症评估单位的一千九十一九十一名患者。 (IADL),迷你营养评估(MNA),Exton-Smith Scale(ESS)和累积疾病评定量表(CIRS)。对于每位患者,应用了Khajuria和Krahn开发的血清渗透压方程。五百七十一名患者具有认知下降和/或抑郁情绪(CD-DM)和520没有CD-DM(对照组)。患有CD-DM的患者不太可能是雄性(P <0.001),更容易较旧(P <0.001),具有显着的认知障碍(MMSE:P <0.001),显示出抑郁症的存在情绪(HDRS-21:P <0.001),与对照组相比,在ADL(P <0.001),IADL(P <0.001),MNA(P <0.001),MNA(P <0.001)中具有重大损伤。 CD-DM患者的电解质浓度较高(Na +:p <0.001; k +:p <0.001; cl:p <0.001),脱水风险(osmolality p <0.001)和肾脏损伤(EGFR:P = 0.021)而不是对照组。阿尔茨海默病(AD)患者表现出电流脱水的主要风险(p≤0.001),脱水与开发痴呆类型的风险有关,如广告或血管痴呆(VAD)(或= 2.016,P <0.001) 。在多变量分析中,脱水状态的存在与Ad1(P <0.001)和IADL(P <0.001)相关,但与年龄单独相关(R2 = 0.0046,p = 0.77),ESS(R2 = 0.0052,P = 0.54)和MNA(R2 = 0.0004,P = 0.48)。此外,痴呆患者的患者比没有痴呆的患者显着脱水(65-75岁,P = 0.001; 76-85岁,P = 0.001;≥86岁,P = 0.293)。膀胱假设旨在解释老年患者的脱水和认知障碍之间的关系,因为蛋白质错误折叠和聚集在存在低间质液体积,这是微循环的缺陷。显示有缺陷的蛋白质损害脑生物分子机制中的信息量,因此神经元和突触损伤。

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