神经退行性变
痴呆
医学
内科学
共病
淀粉样蛋白(真菌学)
疾病
人口
神经病理学
生物标志物
肿瘤科
情感(语言学)
病理
心理学
生物
环境卫生
生物化学
沟通
作者
Jeremy Syrjanen,Michelle R. Campbell,Alicia Algeciras‐Schimnich,Prashanthi Vemuri,Jonathan Graff‐Radford,Mary M. Machulda,Guojun Bu,David S. Knopman,Clifford R. Jack,Ronald C. Petersen,Michelle M. Mielke
摘要
Introduction Blood-based biomarkers of amyloid pathology and neurodegeneration are entering clinical use. It is critical to understand what factors affect the levels of these markers. Methods Plasma markers (Aβ42, Aβ40, NfL, T-tau, Aβ42/40 ratio) were measured on the Quanterix Simoa HD-1 analyzer for 996 Mayo Clinic Study of Aging (MCSA) participants, aged 51 to 95 years. All other data were collected during in-person MCSA visits or abstracted from the medical record. Results Among cognitively unimpaired (CU) participants, all plasma markers correlated with age. Linear regression models revealed multiple relationships. For example, higher Charlson Comorbidity Index and chronic kidney disease were associated with higher levels of all biomarkers. Some relationships differed between mild cognitive impairment and dementia participants. Discussion Multiple variables affect plasma biomarkers of amyloid pathology and neurodegeneration among CU in the general population. Incorporating this information is critical for accurate interpretation of the biomarker levels and for the development of reference ranges.
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