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Medical Histories of Control Subjects Influence the Biomarker Potential of Plasma Aß in Alzheimer's Disease: a Meta-analysis.
Zhang, Shuai; Huang, Si-Yu; An, Xiao-Bin; Zeng, Lu; Ai, Jing.
Afiliación
  • Zhang S; Department of Pharmacology (The State-Province Key Laboratories of Biomedicine-Pharmaceutics of China), College of Pharmacy of Harbin Medical University, Harbin, 150086, Heilongjiang Province, China.
  • Huang SY; Department of Pharmacology (The State-Province Key Laboratories of Biomedicine-Pharmaceutics of China), College of Pharmacy of Harbin Medical University, Harbin, 150086, Heilongjiang Province, China.
  • An XB; Department of Pharmacology (The State-Province Key Laboratories of Biomedicine-Pharmaceutics of China), College of Pharmacy of Harbin Medical University, Harbin, 150086, Heilongjiang Province, China.
  • Zeng L; Department of Pharmacology (The State-Province Key Laboratories of Biomedicine-Pharmaceutics of China), College of Pharmacy of Harbin Medical University, Harbin, 150086, Heilongjiang Province, China.
  • Ai J; Department of Pharmacology (The State-Province Key Laboratories of Biomedicine-Pharmaceutics of China), College of Pharmacy of Harbin Medical University, Harbin, 150086, Heilongjiang Province, China. azhrbmu@126.com.
J Mol Neurosci ; 70(6): 861-870, 2020 Jun.
Article en En | MEDLINE | ID: mdl-32125624
ABSTRACT
Whether blood amyloid-ß (Aß) could be a peripheral biomarker of Alzheimer's disease (AD) remains in dispute. In the present study, we conducted a meta-analysis with 19 citations searched from Embase, PubMed, and the Cochrane Library database. Weighted mean difference (WMD) with 95% confidence intervals (CIs) was used to estimate the effect size. We firstly analyzed the plasma Aß40, Aß42, and Aß42/Aß40 ratio in AD and control group subjects. However, only a lower level of plasma Aß42 was figured out in AD group subjects with weak statistical significance (WMD 1.82; 95% CI 0.59, 3.06; P = 0.004; I2 = 84%). We considered that the medical histories of control subjects could influence the biomarker ability of plasma Aß. Therefore, subgroup analyses were then carried out based on a new recruiting criterion for control subjects, defining as no afflictions of any Aß-related diseases. Surprisingly, AD group subjects showed a significant decrease in plasma Aß42/Aß40 ratio with low heterogeneity among studies (WMD 0.02; 95% CI 0.02, 0.02; P < 0.00001; I2 = 0%). Moreover, not only the Aß42/Aß40 ratio but also Aß42 and Aß40 were indifferent between AD and pseudo-control subjects which might be afflicted with Aß-related diseases. This meta-analysis demonstrated that medical histories of control subjects were interference factors impeding plasma Aß to be a biomarker of AD.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fragmentos de Péptidos / Péptidos beta-Amiloides / Enfermedad de Alzheimer Tipo de estudio: Diagnostic_studies / Systematic_reviews Idioma: En Revista: J Mol Neurosci Asunto de la revista: BIOLOGIA MOLECULAR / NEUROLOGIA Año: 2020 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fragmentos de Péptidos / Péptidos beta-Amiloides / Enfermedad de Alzheimer Tipo de estudio: Diagnostic_studies / Systematic_reviews Idioma: En Revista: J Mol Neurosci Asunto de la revista: BIOLOGIA MOLECULAR / NEUROLOGIA Año: 2020 Tipo del documento: Article