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5-Year mortality predictors in 498,103 UK Biobank participants: a prospective population-based study.
Abstract
Background To our knowledge, a systematic comparison of predictors of mortality in middle-aged to elderly individuals has not yet been done. We investigated predictors of mortality in UK Biobank participants during a 5 year period. We aimed to investigate the associations between most of the available measurements and 5 year all-cause and cause-specific mortality, and to develop and validate a prediction score for 5 year mortality using only self-reported information.Methods Participants were enrolled in the UK Biobank from April, 2007, to July, 2010, from 21 assessment centres across England, Wales, and Scotland with standardised procedures. In this prospective population-based study, we assessed sex-specific associations of 655 measurements of demographics, health, and lifestyle with all-cause mortality and six cause-specific mortality categories in UK Biobank participants using the Cox proportional hazard model. We excluded variables that were missing in more than 80% of the participants and all cardiorespiratory fitness test measurements because summary data were not available. Validation of the prediction score was done in participants enrolled at the Scottish centres. UK life tables and census information were used to calibrate the score to the overall UK population.Findings About 500,000 participants were included in the UK Biobank. We excluded participants with more than 80% variables missing (n=746). Of 498,103 UK Biobank participants included (54% of whom were women) aged 37-73 years, 8532 (39% of whom were women) died during a median follow-up of 4·9 years (IQR 4·33-5·22). Self-reported health (C-index including age 0·74 [95% CI 0·73-0·75]) was the strongest predictor of all-cause mortality in men and a previous cancer diagnosis (0·73 [0·72-0·74]) was the strongest predictor of all-cause mortality in women. When excluding individuals with major diseases or disorders (Charlson comorbidity index >0; n=355 043), measures of smoking habits were the strongest predictors of all-cause mortality. The prognostic score including 13 self-reported predictors for men and 11 for women achieved good discrimination (0·80 [0·77-0·83] for men and 0·79 [0·76-0·83] for women) and significantly outperformed the Charlson comorbidity index (p<0·0001 in men and p=0·0007 in women). A dedicated website allows the interactive exploration of all results along with calculation of individual risk through an online questionnaire.Interpretation Measures that can simply be obtained by questionnaires and without physical examination were the strongest predictors of all-cause mortality in the UK Biobank population. The prediction score we have developed accurately predicts 5 year all-cause mortality and can be used by individuals to improve health awareness, and by health professionals and organisations to identify high-risk individuals and guide public policy.Funding Knut and Alice Wallenberg Foundation and the Swedish Research Council.
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“This may be a consequence of the enrollment bias in the UKB: life tables analysis in36 suggests the UKB subjects appear to outlive typical UK residents.”
From Longitudinal Analysis of Blood Markers Reveals Progressive Loss of Resilience and Predicts Human Lifespan Limit (2021) · cites this paper as [36]
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“slow gait speed has been identified as an independent risk factor for all‐cause mortality 26 , 27”
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“However, self-rated health has been shown to be a good predictor of morbidity, health care utilization, and mortality.15,36”
From Trends in Differences in Health Status and Health Care Access and Affordability by Race and Ethnicity in the United States, 1999–2018 (2021) · cites this paper as [15]
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Global prevalence of sarcopenia and severe sarcopenia: a systematic review and meta‐analysis
Petermann‐Rocha, F., Balntzi, V., Gray, S. R., Lara, J., Ho, F. K., Pell, J. P., & Celis‐Morales, C. (2022) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.12783 · Cited by 1,499
Collider scope: when selection bias can substantially influence observed associations
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Metadata
- Authors
- Ganna, A., & Ingelsson, E.
- Affiliations
- Uppsala University (SE)
- Corresponding author
- Ingelsson, Erik
- Venue
- The Lancet
- Publisher
- Elsevier BV
- Published
- 2015-08
- Volume
- 386
- Issue
- 9993
- Pages
- 533-540
- ISSN
- 0099-5355 (ISSN-L)
- 0140-6736
- OpenAlex
- W2168885178
- Cited by
- 411
- References
- 38
- Citations by year
- 2026: 17 · 2025: 30 · 2024: 43 · 2023: 24 · 2022: 46 · 2021: 37 · 2020: 57 · 2019: 30 · 2018: 34 · 2017: 39 · 2016: 43 · 2015: 11
- FWCI
- 30.74
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Lancet (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Wellcome Trust (093707)
- Topics
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Health and Risk Factors
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Health Promotion and Cardiovascular Prevention
- Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods in Epidemiology
- Keywords
- mortality prediction, all-cause mortality, cause-specific mortality, UK Biobank, self-reported health, smoking, Charlson Comorbidity Index, prognostic score, sex differences, middle-aged and older adults, risk factors
- MeSH terms
- Adult, Aged, Blood Banks, Cause of Death, Female, United Kingdom, Humans, Male, Middle Aged, Predictive Value of Tests, Prognosis, Risk Factors, Cohort Studies, Survival Rate, Proportional Hazards Models
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