Plasma Neurofilament Light Chain and Risk of Death and Stroke in Community-Dwelling Elderly Individuals

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ID: 328906
2026
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Abstract
Abstract Background Circulating neuroinjury biomarkers such as neurofilament light chain (NFL) and glial fibrillary acidic protein (GFAP) have emerged as indicators of brain health. While NFL predicts stroke in patients with atrial fibrillation, its prognostic value in unselected elderly populations is uncertain. We investigated the associations of NFL and GFAP with cardiovascular events and death in community-dwelling older adults. Methods Baseline plasma NFL and GFAP concentrations were determined using high-sensitivity Simoa® assays in 806 participants aged 75 years from the Prospective Investigation of the Vasculature in Uppsala Seniors (PIVUS) study. Cox regression models with sequential adjustment for demographics, comorbidities, renal function, and NT-proBNP assessed associations with ischemic stroke, myocardial infarction, cardiovascular death, all-cause death, and major adverse cardiovascular events (MACE; stroke, myocardial infarction, and all-cause death). Results During a median follow-up of 10 years, 55 ischemic strokes, 48 myocardial infarctions, 52 cardiovascular deaths, and 188 all-cause deaths occurred. NFL was not independently associated with ischemic stroke or myocardial infarction and showed no independent association with cardiovascular death after adjustment including NT-proBNP. In contrast, higher NFL was independently associated with all-cause death (adjusted HR per doubling 1.91; 95% CI 1.49–2.46) and MACE (1.53; 95% CI 1.21–1.93), and improved discrimination for all-cause death beyond established risk factors. GFAP was not associated with any outcome. Conclusions In community-dwelling elderly individuals, higher NFL was associated with increased risk of death but not with specific cardiovascular events. These findings suggest that NFL reflects overall physiological vulnerability rather than discrete vascular risk.
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Authors
Journal European Heart Journal Open
Year 2026
DOI
10.1093/ehjopen/oeag143
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