Leisure time physical activity and bone mineral density preservation during the menopause transition and postmenopause: a longitudinal cohort analysis from the Study of Women's Health Across the Nation (SWAN).

Bone mineral density Menopause Physical activity Women

Journal

Lancet regional health. Americas
ISSN: 2667-193X
Titre abrégé: Lancet Reg Health Am
Pays: England
ID NLM: 9918232503006676

Informations de publication

Date de publication:
May 2023
Historique:
received: 25 08 2022
revised: 28 02 2023
accepted: 10 03 2023
medline: 4 4 2023
entrez: 3 4 2023
pubmed: 4 4 2023
Statut: epublish

Résumé

Whether greater leisure time physical activity (LTPA) is associated with less bone mineral density (BMD) loss during the menopause transition (MT) remains an open question. We hypothesized that: 1) larger increases in LTPA from pre-/early perimenopause (period 1) to late perimenopause/postmenopause (period 2) would be associated with a slower period 2 BMD loss rate; and 2) greater entire-study LTPA levels would be associated with better final absolute BMD (g/cm Data were from of the Study of Women's Health Across the Nation (1996-2017). Exclusions were: bone beneficial medications, inability to identify start of the MT, and extreme BMD change rates. LTPA measures were a validated ordinal scale and number of metabolic equivalents per hour per week (MET hr wk Median [p25, p75] MET hr wk Findings suggest that LTPA, at modest levels, mitigate MT-related BMD decline and even small increases in intensity, duration or frequency of common activities may lessen bone loss at the population level. US-NIH.

Sections du résumé

Background UNASSIGNED
Whether greater leisure time physical activity (LTPA) is associated with less bone mineral density (BMD) loss during the menopause transition (MT) remains an open question. We hypothesized that: 1) larger increases in LTPA from pre-/early perimenopause (period 1) to late perimenopause/postmenopause (period 2) would be associated with a slower period 2 BMD loss rate; and 2) greater entire-study LTPA levels would be associated with better final absolute BMD (g/cm
Methods UNASSIGNED
Data were from of the Study of Women's Health Across the Nation (1996-2017). Exclusions were: bone beneficial medications, inability to identify start of the MT, and extreme BMD change rates. LTPA measures were a validated ordinal scale and number of metabolic equivalents per hour per week (MET hr wk
Findings UNASSIGNED
Median [p25, p75] MET hr wk
Interpretation UNASSIGNED
Findings suggest that LTPA, at modest levels, mitigate MT-related BMD decline and even small increases in intensity, duration or frequency of common activities may lessen bone loss at the population level.
Funding UNASSIGNED
US-NIH.

Identifiants

pubmed: 37008197
doi: 10.1016/j.lana.2023.100481
pii: S2667-193X(23)00055-8
pmc: PMC10060105
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100481

Subventions

Organisme : NIA NIH HHS
ID : P30 AG024824
Pays : United States
Organisme : NIA NIH HHS
ID : U19 AG063720
Pays : United States

Informations de copyright

© 2023 The Authors.

Déclaration de conflit d'intérêts

All authors declare that they have no financial relationships with any organisation that might have an interest in the submitted work and have no other relationships or activities that could appear to have influenced the submitted work.

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Auteurs

Gail A Greendale (GA)

Department of Medicine, Division of Geriatrics, UCLA, Los Angeles, CA, USA.

Nicholas J Jackson (NJ)

Department of Medicine, Division of General Internal Medicine, UCLA, Los Angeles, CA, USA.

Albert Shieh (A)

Department of Medicine, Division of Geriatrics, UCLA, Los Angeles, CA, USA.

Jane A Cauley (JA)

Department of Epidemiology, School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.

Carrie Karvonen-Gutierrez (C)

Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI, USA.

Kelly R Ylitalo (KR)

Department of Public Health, Robbins College of Health and Human Sciences, Baylor University, Waco, TX, USA.

Kelley Pettee Gabriel (KP)

Department of Epidemiology, School of Public Health, University of Alabama at Birmingham, Birmingham, AL, USA.

Barbara Sternfeld (B)

Division of Research, Kaiser Permanente Northern California, Oakland, CA, USA.

Arun S Karlamangla (AS)

Department of Medicine, Division of Geriatrics, UCLA, Los Angeles, CA, USA.

Classifications MeSH