Evidence map›Paper›PMID 42587017›Full record

ArticleInternational journal of obesity (2005)2026

Adolescent weight gain trajectories and their associations with biological aging: a genetically informed study.

Anni Pitkänen, Anna Kankaanpää, Emma Raitoharju, Saara Marttila, Leo-Pekka Lyytikäinen, Pashupati P Mishra, Nina Mononen, Tuija Tammelin, Juha Mykkänen, Katja Pahkala and 7 more

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Article in International journal of obesity (2005), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

17 authors.

Anni PitkänenFaculty of Sport and Health Sciences Gerontology Research Center (GEREC), University of Jyväskylä, Jyväskylä, Finland.ORCID http://orcid.org/0009-0003-7866-144X
Anna KankaanpääFaculty of Sport and Health Sciences Gerontology Research Center (GEREC), University of Jyväskylä, Jyväskylä, Finland.ORCID http://orcid.org/0000-0002-6973-5385
Emma RaitoharjuFinnish Cardiovascular Research Center Tampere, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Saara MarttilaGerontology Research Center (GEREC), Tampere University, Tampere, Finland.
Leo-Pekka LyytikäinenGerontology Research Center (GEREC), Tampere University, Tampere, Finland.ORCID http://orcid.org/0000-0002-7200-5455
Pashupati P MishraGerontology Research Center (GEREC), Tampere University, Tampere, Finland.
Nina MononenClinical Chemistry, Tampere University Hospital, and Finnish Cardiovascular Research Center - Tampere, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Tuija TammelinLikes, Jamk University of Applied Sciences, School of Health and Social Studies, Jyväskylä, Finland.ORCID http://orcid.org/0000-0002-1771-3977
Juha MykkänenCentre for Population Health Research, University of Turku and Turku University Hospital, Turku, Finland.
Katja PahkalaCentre for Population Health Research, University of Turku and Turku University Hospital, Turku, Finland.
Suvi RovioCentre for Population Health Research, University of Turku and Turku University Hospital, Turku, Finland.
Laura JoensuuFaculty of Sport and Health Sciences Gerontology Research Center (GEREC), University of Jyväskylä, Jyväskylä, Finland.ORCID http://orcid.org/0000-0002-9544-6552
Miina OllikainenInstitute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Helsinki, Finland.ORCID http://orcid.org/0000-0003-3661-7400
Jorma ViikariDepartment of Medicine, University of Turku, Turku, Finland.ORCID http://orcid.org/0000-0001-6452-010X
Olli RaitakariCentre for Population Health Research, University of Turku and Turku University Hospital, Turku, Finland.
Terho LehtimäkiGerontology Research Center (GEREC), Tampere University, Tampere, Finland.ORCID http://orcid.org/0000-0002-2555-4427
Elina SillanpääFaculty of Sport and Health Sciences, University of Jyväskylä, Jyväskylä, Finland. elina.sillanpaa@jyu.fi.ORCID http://orcid.org/0000-0001-6375-959X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHigh body mass index (BMI) in adolescence is associated with accelerated biological aging, which might predict the onset of obesity-related diseases before they develop. Genetic factors may shape both adolescent BMI and weight trajectories.

methodsParticipants were from the Young Finns Study (n = 3 596, ages 3-18 at baseline), followed from 1980 to 2018-2020. Biological aging was estimated using DNA methylation based epigenetic clocks DunedinPACE (years/calendar year) and PC-GrimAge (years) at three follow-ups (ages 15-56, n = 2045). Genetic predispositions to BMI and childhood body size were quantified using polygenic risk scores (PRSs) (941 and 286 genetic variants). BMI trajectories were modelled from BMI measured at ages 9, 12, 15 and 18 using latent growth curve modelling. Path analysis was used to examine whether genetic liability to BMI is associated with biological aging and if BMI trajectories in adolescence mediate this association. The causal effect of genetically predicted adolescent BMI on biological aging in adulthood was examined with Mendelian randomisation (MR) using individual-level data.

resultsHigher level of adolescent BMI partly mediated the association between higher BMI-PRS and accelerated biological aging from late adolescence to middle adulthood. MR analyses supported a positive causal effect from genetically predicted adolescent BMI on biological aging, and the causal effect was more consistent when DunedinPACE was used to measure biological aging in 2011 (causal estimate = 0.020 [95% CI = 0.008, 0.031]) and 2018 (0.019 [0.003, 0.035]).

conclusionsOur findings indicate that high BMI in adolescence may accelerate biological aging, especially in individuals with a genetic predisposition to high BMI. Adolescents with a genetic susceptibility to high BMI and elevated BMI might be prone to obesity-related health risks, highlighting early prevention strategies' importance.

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.