A1 Refereed original research article in a scientific journal

Factors related to blood-based biomarkers for neurodegenerative diseases and their intergenerational associations in the Young Finns Study: a cohort study




AuthorsHeiskanen, Marja A; Mykkänen, Juha; Pahkala, Katja; Juonala, Markus; Kähönen, Mika; Lehtimäki, Terho; Laitinen, Tomi P; Jokinen, Eero; Tossavainen, Päivi; Linko-Parvinen, Anna; Pallari, Hanna-Mari; Blennow, Kaj; Zetterberg, Henrik; Viikari, Jorma; Raitakari, Olli; Rovio, Suvi P

PublisherElsevier BV

Publishing placeAMSTERDAM

Publication year2025

JournalThe Lancet healthy longevity

Journal name in sourceThe Lancet Healthy Longevity

Journal acronymLANCET HEALTH LONGEV

Article number100717

Volume6

Issue6

Number of pages12

ISSN2666-7568

DOIhttps://doi.org/10.1016/j.lanhl.2025.100717

Web address https://doi.org/10.1016/j.lanhl.2025.100717

Self-archived copy’s web addresshttps://research.utu.fi/converis/portal/detail/Publication/499504135


Abstract
Background: Blood-based biomarkers (BBM) of neurodegenerative diseases are emerging as cost-effective tools in the differential diagnostics of Alzheimer's disease and other dementias. Scarce data exist about factors explaining BBM variation in population-based cohorts, and their intergenerational associations are unknown. This study aimed to characterise BBM distributions among a population-based cohort, investigate the association of a wide array of factors with BBM both in midlife and old age, and investigate intergenerational associations of BBM. Methods: We measured BBM detecting amyloid beta and tau pathologies, including amyloid beta 42, amyloid beta 40, and phosphorylated Tau (pTau)-217, as well as glial fibrillary acidic protein (GFAP) and neurofilament light chain (NfL) in the multigenerational Young Finns Study participants (n=1237, age 41-56 years) and their parents (n=814, age 59-90 years) using the Quanterix Simoa HD-X analyser. Standard statistical methods were used to examine the associations between BBM and age, sex, genetic factors, a plethora of cardiometabolic markers, liver and kidney function, and lifestyle factors, as well as their intergenerational associations. Findings: Increased age was associated with adverse BBM concentrations. Of the various investigated factors, the most robust associations towards adverse BBM concentration were found for APOE epsilon 4 carrier status among parents (amyloid beta 42:40 ratio, pTau-217, and GFAP) and high serum creatinine concentration in both generations (pTau-217, GFAP, and NfL). Several factors related to glucose metabolism and dyslipidaemia were negatively associated with all BBM, but adjusting for BMI diluted many of these associations. Statistically significant intergenerational correlations ranged from 020 to 033 and were mostly observed between mothers and offspring in pTau-217, GFAP, and NfL. No intergenerational correlations existed in amyloid beta 42:40 ratio. Interpretation: We identified several factors that might influence BBM concentrations, parental transmission being one of them. For reliable use of BBM in clinical practice, it is important to identify which factors directly link to amyloid beta and tau pathology and which factors influence BBM concentrations due to other physiological processes. Copyright (c) 2025 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-NDlicense (http://creativecommons.org/licenses/by-nc-nd/4.0/)

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Funding information in the publication
Research Council of Finland, Social Insurance Institution of Finland, Competitive State Research Financing of the Expert Responsibility area of the Kuopio, Tampere and Turku University Hospitals, Juho Vainio Foundation, Paavo Nurmi Foundation, Finnish Foundation for Cardiovascular Research, Finnish Cultural Foundation, The Sigrid Juselius Foundation, Tampere Tuberculosis Foundation, Emil Aaltonen Foundation, Yrjoe Jahnsson Foundation, Signe and Ane Gyllenberg Foundation, Jenny and Antti Wihuri Foundation, Diabetes Research Foundation of the Finnish Diabetes Association, EU Horizon 2020, European Research Council, Tampere University Hospital Supporting Foundation, Finnish Society of Clinical Chemistry, the Jane and Aatos Erkko Foundation, and the Finnish Brain Foundation.


Last updated on 2025-05-09 at 12:49