轻度认知障碍和痴呆症的代谢和环境生物标志物:一项探索性研究

IF 1.3 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Journal of Integrative and Complementary Medicine Pub Date : 2024-08-01 Epub Date: 2024-02-08 DOI:10.1089/jicm.2023.0583
Abigail C Lyon, Carol F Lippa, Arnold R Eiser
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引用次数: 0

摘要

目的确定通过常见血液检测在认知障碍患者中发现可疑致病因素(包括可能导致阿尔茨海默病(AD)的金属和代谢物)的频率。检测方法在两个队列(一个符合轻度认知障碍(MCI)标准,另一个符合轻度至中度痴呆(DE)标准)中测量了各种血清检测项目,包括金属、氨、同型半胱氨酸、维生素 B12、叶酸、甲状腺检测、代谢产物和炎症标记物。此外,还对这些患者所服用的药物进行了复查。结果显示半数以上受试者检测到金属异常,包括汞、铅和砷升高的证据,以及必需金属、铁(Fe)和铜超标的情况。64%的 DE 组和 66% 的 MCI 组检测到了某些金属畸变。女性更容易出现铜升高,这与荷尔蒙对铜排泄的影响一致。同型半胱氨酸血症是最常见的异常,在71%的DE患者和67%的MCI患者中被检测到,而甲基丙二酸没有升高。轻微的高氨血症较为常见(38%),这表明该亚群中存在肝脏因素。近一半的患者(44% DE,52% MCI)存在中度胰岛素抵抗。65 人中有 60 人(92%)至少有一种生物标志物异常,60% 的人有两种或两种以上的生物标志物异常。所有患者最常服用的药物是质子泵抑制剂,其中 22% 为 DE 型,38% 为 MCI 型。结论这项研究表明,在 MCI 和 DE 的两个阶段都能检测到有毒金属和过量的重要金属(如铜和铁),以及常见的代谢和肝脏因素。导致 DE 的诱发因素似乎多种多样。基于这些参数的个体化干预可能是减少认知能力下降导致 DE 的一种手段。看来有必要对这些环境和代谢因素进行更全面的前瞻性研究,并及早采取纠正性干预措施。
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Metabolic and Environmental Biomarkers in Mild Cognitive Impairment and Dementia: An Exploratory Study.

Objective: To determine the frequency with which suspected pathogenic factors, including metals and metabolites that might contribute to Alzheimer's disease (AD), may be found in patients with cognitive impairment through commonly available blood tests. Methods: A variety of serum studies, including metals, ammonia, homocysteine, vitamin B12, folate, thyroid tests, metabolic products, and inflammatory markers, were measured in two cohorts: one meeting mild cognitive impairment (MCI) criteria and the other meeting mild-to-moderate dementia (DE) criteria. Medications these patients received were reviewed. Results: Metal abnormalities were detected in over half the subjects, including evidence of mercury, lead, and arsenic elevation as well as instances of excessive essential metals, iron (Fe), and copper. Some metal aberration was detected in 64% of the DE group and 66% of the MCI group. Females were more likely to have elevated copper, consistent with hormonal effects on copper excretion. Homocysteinemia was the most common abnormality, detected in 71% with DE and 67% with MCI, while methylmalonic acid was not elevated. Slight hyperammonemia was moderately common (38%) suggesting a hepatic factor in this subset. Findings of moderate insulin resistance were present in nearly half (44% DE, 52% MCI). Sixty of 65 (92%) had at least one abnormal biomarker and 60% had two or more. The most common drug taken by the total cohort was proton pump inhibitors at 22% DE and 38% MCI. Conclusions: This study suggests that both toxic metals and excessive vital metals such as copper and iron, as well as common metabolic and hepatic factors are detectable at both stages of MCI and DE. There appears to be a multiplicity of provocative factors leading to DE. Individualized interventions based on these parameters may be a means to reduce cognitive decline leading to DE. A more comprehensive prospective study of these environmental and metabolic factors with corrective early interventions appears warranted.

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