Evidence map›Paper›PMID 40643204›Full record

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

Type 1 and 2 diabetes mellitus: comprehensive fracture risk relationships in UK Biobank.

Elizabeth M Curtis, Rebecca J Moon, Stefania D'Angelo, Zahra Raisi-Estabragh, Cyrus Cooper, Nicholas C Harvey

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. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

6 authors.

Elizabeth M CurtisMRC Lifecourse Epidemiology Centre, University of Southampton, Southampton General Hospital, Southampton SO16 6YD, United Kingdom.
Rebecca J MoonMRC Lifecourse Epidemiology Centre, University of Southampton, Southampton General Hospital, Southampton SO16 6YD, United Kingdom.ORCID 0000-0003-2334-2284
Stefania D'AngeloMRC Lifecourse Epidemiology Centre, University of Southampton, Southampton General Hospital, Southampton SO16 6YD, United Kingdom.ORCID 0000-0002-7267-1837
Zahra Raisi-EstabraghBarts Heart Centre, St Bartholomew's Hospital, Barts Health NHS Trust, London EC1A 7BE, United Kingdom.
Cyrus CooperMRC Lifecourse Epidemiology Centre, University of Southampton, Southampton General Hospital, Southampton SO16 6YD, United Kingdom.ORCID 0000-0003-3510-0709
Nicholas C HarveyMRC Lifecourse Epidemiology Centre, University of Southampton, Southampton General Hospital, Southampton SO16 6YD, United Kingdom.ORCID 0000-0002-8194-2512

Funding

American Society for Bone and Mineral ResearchNational Institute for Health Research NIHR305844NIHR Academic Clinical LectureshipNIHR Integrated Academic Training programmeNIHR Oxford Biomedical Research CentreNIHR Southampton Biomedical Research Centre NIHR203319UK Medical Research Council MC_PC_21001UK Medical Research Council MC_PC_21003University of OxfordUniversity of Southampton, and University Hospital Southampton NHS Foundation TrustWellcome TrustWellcome Trust 201268/Z/16/ZWellcome Trust 209233/Z/17/Z
6 · The paper itself

Abstract

We aimed to investigate associations between diabetes mellitus and incident fracture, stratified by diabetes type (1 or 2), disease duration and microvascular complications of diabetes. This prospective cohort analysis used data from the UK Biobank, a large population-based cohort of participants recruited 2006-2010 at age 40-69 yr. The exposure was type 1 or type 2 diabetes at baseline, with the outcome of first incident osteoporotic fracture. Poisson regression was used to calculate incidence rate ratios (IRRs) for osteoporotic fracture to investigate prospective relationships between diabetes type 1 or 2 and fracture risk independent of traditional clinical risk factors, estimated BMD by heel ultrasound (eBMD), adiposity, and C-reactive protein (CRP). The role of diabetic microvascular complications and associations between diabetes duration and fracture risk were studied. There were 498 949 participants (271 882 women, mean age 56 yr; 227 067 men, 57 yr). In fully adjusted models, type 1 and 2 diabetes were associated with increased fracture risk [type 1; IRR: 2.93 (95% CI: 2.37, 3.62); type 2: 1.25 (1.14, 1.38)], similar by sex. The magnitude of risk associated with type 2 diabetes increased with the duration of disease. Increasing number of microvascular complications was associated with greater fracture risk [any vs no complications, IRR 2.03 (1.57, 2.62)]. Diabetes is associated with increased risk of fracture (magnitude of effect greater in type 1 than type 2 diabetes). Associations were partly independent of traditional risk factors, adiposity, eBMD, and CRP. Type 2 diabetes disease duration and the presence of microvascular complications in both types were dose-dependent risk factors for fracture.

Indexed as

Biological Specimen BanksDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2Fractures, BoneOsteoporotic FracturesAdultAgedBone DensityFemaleHumansMaleMiddle AgedProspective StudiesRisk FactorsUK BiobankUnited Kingdomepidemiologyfractureosteoporosistype 1 diabetes mellitustype 2 diabetes mellitus

Identifiers

PMID40643204
PMCPMC12578282

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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 OpenQuestion graph.