Evidence map›Paper›PMID 40747984›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2025

Plasma fatty acid composition predicts bone mineral accrual from childhood to adolescence: the Physical Activity and Nutrition in Children study.

Timo A Lakka, Saara Heinonen, Taisa Sallinen, Aino-Maija Eloranta, Suvi Laamanen, Annie M Skinner, Eero A Haapala, Dimitris Vlachopoulos, Alan R Barker, Toni Rikkonen and 3 more

Abstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Timo A LakkaInstitute of Biomedicine, School of Medicine, Faculty of Health Sciences, University of Eastern Finland, 70211 Kuopio, Finland.ORCID 0000-0002-9199-2871
Saara HeinonenInstitute of Biomedicine, School of Medicine, Faculty of Health Sciences, University of Eastern Finland, 70211 Kuopio, Finland.
Taisa SallinenInstitute of Biomedicine, School of Medicine, Faculty of Health Sciences, University of Eastern Finland, 70211 Kuopio, Finland.ORCID 0000-0003-2769-6338
Aino-Maija ElorantaInstitute of Biomedicine, School of Medicine, Faculty of Health Sciences, University of Eastern Finland, 70211 Kuopio, Finland.
Suvi LaamanenInstitute of Public Health and Clinical Nutrition, School of Medicine, Faculty of Health Sciences, University of Eastern Finland, 70210 Kuopio, Finland.ORCID 0000-0001-9168-3457
Annie M SkinnerChildren's Health and Exercise Research Centre, University of Exeter, Exeter EX1 2LU, United Kingdom.
Eero A HaapalaInstitute of Biomedicine, School of Medicine, Faculty of Health Sciences, University of Eastern Finland, 70211 Kuopio, Finland.ORCID 0000-0001-5096-851X
Dimitris VlachopoulosChildren's Health and Exercise Research Centre, University of Exeter, Exeter EX1 2LU, United Kingdom.ORCID 0000-0003-1556-715X
Alan R BarkerChildren's Health and Exercise Research Centre, University of Exeter, Exeter EX1 2LU, United Kingdom.ORCID 0000-0001-8610-5417
Toni RikkonenKuopio Musculoskeletal Research Unit (KMRU), University of Eastern Finland, 70210 Kuopio, Finland.ORCID 0000-0001-5948-1222
Tomi P LaitinenDepartment of Clinical Physiology and Nuclear Medicine, Kuopio University Hospital, Wellbeing Services County of North Savo, 70210 Kuopio, Finland.ORCID 0000-0003-3553-9957
Jyrki ÅgrenInstitute of Biomedicine, School of Medicine, Faculty of Health Sciences, University of Eastern Finland, 70211 Kuopio, Finland.
Sonja SoininenInstitute of Biomedicine, School of Medicine, Faculty of Health Sciences, University of Eastern Finland, 70211 Kuopio, Finland.ORCID 0000-0002-2082-8652

Funding

Diabetes Research Foundation in FinlandFinnish Cultural FoundationFinnish Foundation for Cardiovascular ResearchFinnish Innovation Fund SitraFoundation for Pediatric ResearchJuho Vainio FoundationMinistry of Education and Culture of FinlandMinistry of Social Affairs and Health of FinlandOrion Research FoundationPaavo Nurmi FoundationResearch Committee of the Kuopio University Hospital Catchment AreaSocial Insurance Institution of FinlandYrjö Jahnsson Foundation
6 · The paper itself

Abstract

Little is known about the associations of plasma fatty acids (FAs) with bone mineral accrual, and the evidence is mostly based on cross-sectional data. In this observational study, we investigated for the first time the longitudinal associations of plasma FA composition as well as desaturase and elongase enzyme activities with BMD from childhood to adolescence. Altogether, 480 children (227 girls) aged 7-9 yr attending baseline examinations were included in the current analyses. The longitudinal associations of the proportions of FAs in plasma phospholipids, analyzed by gas chromatography, as well as estimated desaturase and elongase activities with total body less head BMD, measured by dual-energy X-ray absorptiometry, were analyzed by linear mixed-effects models using values from baseline, 2-yr, and 8-yr follow-up and adjusted for sex, maturity offset, follow-up time, and lean mass (LM) or fat mass (FM). Decreased proportion of linoleic acid (standardized regression coefficient β = -.023, p = .001), increased proportion of dihomo-gamma-linolenic acid (β = .029, p < .001), and Δ6-desaturase activity (β = .032, p < .001) were associated with increased BMD independent of sex, maturity offset, follow-up time, LM, and FM. Increased proportions of nervonic acid (β = .018, p = .012), arachidonic acid (β = .019, p = .017), and docosapentaenoic acid (β = .020, p = .013) were associated with increased BMD, and these associations were partly explained by LM. Increased proportions of arachidic acid (β = .022, p = .005), behenic acid (β = .018, p = .010), lignoceric acid (β = .015, p = .040), and palmitoleic acid (β = .016, p = .013), increased stearoyl-CoA-desaturase activity (β = .017, p = .009), and decreased elongase activity (β = -.017, p = .023) were associated with increased BMD, and these associations were partly explained by FM. Single plasma saturated, monounsaturated, and polyunsaturated FAs have divergent longitudinal associations with BMD from childhood to adolescence. Plasma FA composition predicts bone mineral accrual from childhood to adolescence, implying that FA metabolism is important for healthy bone development since childhood.

Indexed as

Bone DensityExerciseFatty AcidsNutritional StatusAdolescentChildFatty Acid DesaturasesFemaleHumansLongitudinal StudiesMaleFatty Acid DesaturasesFatty Acidsadolescentbone mineral densitychilddual-energy X-ray absorptiometryfatty acidphospholipid

Identifiers

PMID40747984
PMCPMC12578281

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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 OpenQuestion graph.