Evidence map›Paper›PMID 27472291›Full record

ArticleThe Journal of clinical endocrinology and metabolism2016

Menopause, Reproductive Life, Hormone Replacement Therapy, and Bone Phenotype at Age 60-64 Years: A British Birth Cohort.

D Kuh, S Muthuri, R Cooper, A Moore, K Mackinnon, C Cooper, J E Adams, R Hardy, K A Ward

Abstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
–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

17 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Physical Activity Across Adulthood and Bone Health in Later Life: The 1946 British Birth Cohort.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2019
    Trial
  3. Article
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  6. Trabecular bone deficits predominate in the appendicular skeleton of midlife women living with HIV: findings from a cross-sectional study in Zimbabwe.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2025
    Article
  7. Review
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  12. Age-, Site-, and Sex-Specific Normative Centile Curves for HR-pQCT-Derived Microarchitectural and Bone Strength Parameters in a Chinese Mainland Population.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2020
    Article
  13. Review
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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

9 authors.

D KuhMedical Research Council Unit for Lifelong Health and Ageing (D.K., S.M., R.C., A.M., K.M., R.H.), University College London, London WC1B 5JU, United Kingdom; Medical Research Council Lifecourse Epidemiology Unit (C.C., K.A.W.), University of Southampton, Southampton SO16 6YD, United Kingdom; Clinical Radiology and Academic Health Science Centre (J.E.A.), Manchester Royal Infirmary, Central Manchester University Hospital, National Health Service Foundation Trust and University of Manchester, Manchester M13 9PT, United Kingdom; and Medical Research Council Human Nutrition Research (K.A.W.), Cambridge CB1 9NL, United Kingdom.
S MuthuriMedical Research Council Unit for Lifelong Health and Ageing (D.K., S.M., R.C., A.M., K.M., R.H.), University College London, London WC1B 5JU, United Kingdom; Medical Research Council Lifecourse Epidemiology Unit (C.C., K.A.W.), University of Southampton, Southampton SO16 6YD, United Kingdom; Clinical Radiology and Academic Health Science Centre (J.E.A.), Manchester Royal Infirmary, Central Manchester University Hospital, National Health Service Foundation Trust and University of Manchester, Manchester M13 9PT, United Kingdom; and Medical Research Council Human Nutrition Research (K.A.W.), Cambridge CB1 9NL, United Kingdom.
R CooperMedical Research Council Unit for Lifelong Health and Ageing (D.K., S.M., R.C., A.M., K.M., R.H.), University College London, London WC1B 5JU, United Kingdom; Medical Research Council Lifecourse Epidemiology Unit (C.C., K.A.W.), University of Southampton, Southampton SO16 6YD, United Kingdom; Clinical Radiology and Academic Health Science Centre (J.E.A.), Manchester Royal Infirmary, Central Manchester University Hospital, National Health Service Foundation Trust and University of Manchester, Manchester M13 9PT, United Kingdom; and Medical Research Council Human Nutrition Research (K.A.W.), Cambridge CB1 9NL, United Kingdom.
A MooreMedical Research Council Unit for Lifelong Health and Ageing (D.K., S.M., R.C., A.M., K.M., R.H.), University College London, London WC1B 5JU, United Kingdom; Medical Research Council Lifecourse Epidemiology Unit (C.C., K.A.W.), University of Southampton, Southampton SO16 6YD, United Kingdom; Clinical Radiology and Academic Health Science Centre (J.E.A.), Manchester Royal Infirmary, Central Manchester University Hospital, National Health Service Foundation Trust and University of Manchester, Manchester M13 9PT, United Kingdom; and Medical Research Council Human Nutrition Research (K.A.W.), Cambridge CB1 9NL, United Kingdom.
K MackinnonMedical Research Council Unit for Lifelong Health and Ageing (D.K., S.M., R.C., A.M., K.M., R.H.), University College London, London WC1B 5JU, United Kingdom; Medical Research Council Lifecourse Epidemiology Unit (C.C., K.A.W.), University of Southampton, Southampton SO16 6YD, United Kingdom; Clinical Radiology and Academic Health Science Centre (J.E.A.), Manchester Royal Infirmary, Central Manchester University Hospital, National Health Service Foundation Trust and University of Manchester, Manchester M13 9PT, United Kingdom; and Medical Research Council Human Nutrition Research (K.A.W.), Cambridge CB1 9NL, United Kingdom.
C CooperMedical Research Council Unit for Lifelong Health and Ageing (D.K., S.M., R.C., A.M., K.M., R.H.), University College London, London WC1B 5JU, United Kingdom; Medical Research Council Lifecourse Epidemiology Unit (C.C., K.A.W.), University of Southampton, Southampton SO16 6YD, United Kingdom; Clinical Radiology and Academic Health Science Centre (J.E.A.), Manchester Royal Infirmary, Central Manchester University Hospital, National Health Service Foundation Trust and University of Manchester, Manchester M13 9PT, United Kingdom; and Medical Research Council Human Nutrition Research (K.A.W.), Cambridge CB1 9NL, United Kingdom.
J E AdamsMedical Research Council Unit for Lifelong Health and Ageing (D.K., S.M., R.C., A.M., K.M., R.H.), University College London, London WC1B 5JU, United Kingdom; Medical Research Council Lifecourse Epidemiology Unit (C.C., K.A.W.), University of Southampton, Southampton SO16 6YD, United Kingdom; Clinical Radiology and Academic Health Science Centre (J.E.A.), Manchester Royal Infirmary, Central Manchester University Hospital, National Health Service Foundation Trust and University of Manchester, Manchester M13 9PT, United Kingdom; and Medical Research Council Human Nutrition Research (K.A.W.), Cambridge CB1 9NL, United Kingdom.
R HardyMedical Research Council Unit for Lifelong Health and Ageing (D.K., S.M., R.C., A.M., K.M., R.H.), University College London, London WC1B 5JU, United Kingdom; Medical Research Council Lifecourse Epidemiology Unit (C.C., K.A.W.), University of Southampton, Southampton SO16 6YD, United Kingdom; Clinical Radiology and Academic Health Science Centre (J.E.A.), Manchester Royal Infirmary, Central Manchester University Hospital, National Health Service Foundation Trust and University of Manchester, Manchester M13 9PT, United Kingdom; and Medical Research Council Human Nutrition Research (K.A.W.), Cambridge CB1 9NL, United Kingdom.
K A WardMedical Research Council Unit for Lifelong Health and Ageing (D.K., S.M., R.C., A.M., K.M., R.H.), University College London, London WC1B 5JU, United Kingdom; Medical Research Council Lifecourse Epidemiology Unit (C.C., K.A.W.), University of Southampton, Southampton SO16 6YD, United Kingdom; Clinical Radiology and Academic Health Science Centre (J.E.A.), Manchester Royal Infirmary, Central Manchester University Hospital, National Health Service Foundation Trust and University of Manchester, Manchester M13 9PT, United Kingdom; and Medical Research Council Human Nutrition Research (K.A.W.), Cambridge CB1 9NL, United Kingdom.

Funding

Medical Research Council G0400491Medical Research Council MC_U105960371Medical Research Council MC_U147585819Medical Research Council MC_U147585824Medical Research Council MC_U147585827Medical Research Council MC_UP_A620_1014Medical Research Council MC_UU_12011/1Medical Research Council MC_UU_12019/4
6 · The paper itself

Abstract

contextPrevious studies of menopausal age and length of reproductive life on bone are limited by retrospective reproductive histories, being cross-sectional, or lacking gold standard bone technologies or information on hormone replacement therapy (HRT) or surgical treatment.

objectiveThe objective of the study was to investigate age at menopause, length of reproductive life, and HRT use in relation to volumetric and areal bone mineral density (vBMD, aBMD), bone size, and strength in women aged 60-64 years.

designThis was a birth cohort study that followed up for 64 years with prospective measures of age at menarche and menopause and monthly HRT histories.

settingThe study was conducted in England, Scotland, and Wales.

participantsParticipants included 848 women with a known type of menopause and bone measures at 60-64 years.

main outcome measuresPeripheral quantitative computed tomography measurements of the distal radius total and trabecular vBMD were measured. Diaphyseal radius total and medullary cross-sectional area, cortical vBMD, and polar strength strain index (SSI); dual-energy x-ray absorptiometry measurements of aBMD at the lumbar spine and total hip were also measured.

resultsA 10-year increase in age at natural (but not surgical) menopause was associated with 8.2% (95% confidence interval [CI] 1.3%-15.1%, P = .02) greater trabecular vBMD and a 6.0% (95% CI 0.51%-11.5%, P = .03) greater total vBMD; findings were similar for length of reproductive life. A 10-year difference in HRT use was associated with a 6.0% (95% CI 2.6%-9.3%, P < .001) greater polar SSI and a 0.9% (95% CI 0.4%-1.5%, P = .001) greater cortical vBMD. These estimates changed little on adjustment. Estimates for aBMD were consistent with those for peripheral quantitative computed tomography.

conclusionsThe positive effects on trabecular vBMD of later natural menopause and longer reproductive life persisted into early old age. HRT use was associated with greater radius cortical vBMD and polar SSI and aBMD.

Indexed as

Absorptiometry, PhotonAge FactorsBone and BonesBone DensityEnglandFemaleHormone Replacement TherapyHumansLongitudinal StudiesMenarcheMenopauseMiddle AgedPhenotypeScotlandTime FactorsWales

Identifiers

PMID27472291
PMCPMC5052353

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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.