Phenotypes of Polish primary care patients using hierarchical clustering: Exploring the risk of mortality in the LIPIDOGEN2015 study cohort.

ageing hierarchical clustering mortality obesity primary care protein thiol groups

Journal

European journal of clinical investigation
ISSN: 1365-2362
Titre abrégé: Eur J Clin Invest
Pays: England
ID NLM: 0245331

Informations de publication

Date de publication:
08 Jun 2024
Historique:
revised: 17 05 2024
received: 09 04 2024
accepted: 29 05 2024
medline: 8 6 2024
pubmed: 8 6 2024
entrez: 8 6 2024
Statut: aheadofprint

Résumé

Comorbidities in primary care do not occur in isolation but tend to cluster together causing various clinically complex phenotypes. This study aimed to distinguish phenotype clusters and identify the risks of all-cause mortality in primary care. The baseline cohort of the LIPIDOGEN2015 sub-study involved 1779 patients recruited by 438 primary care physicians. To identify different phenotype clusters, we used hierarchical clustering and investigated differences between clinical characteristics and mortality between clusters. We then performed causal analyses using causal mediation analysis to explore potential mediators between different clusters and all-cause mortality. A total of 1756 patients were included (mean age 51.2, SD 13.0; 60.3% female), with a median follow-up of 5.7 years. Three clusters were identified: Cluster 1 (n = 543) was characterised by overweight/obesity (body mass index ≥ 25 kg/m Overweight/obesity older patients with more comorbidities had the highest risk of long-term all-cause mortality, and in the young group population overweight/obesity insignificantly increased the risk in the long-term follow-up, providing a basis for stratified phenotypic risk management.

Sections du résumé

BACKGROUND BACKGROUND
Comorbidities in primary care do not occur in isolation but tend to cluster together causing various clinically complex phenotypes. This study aimed to distinguish phenotype clusters and identify the risks of all-cause mortality in primary care.
METHODS METHODS
The baseline cohort of the LIPIDOGEN2015 sub-study involved 1779 patients recruited by 438 primary care physicians. To identify different phenotype clusters, we used hierarchical clustering and investigated differences between clinical characteristics and mortality between clusters. We then performed causal analyses using causal mediation analysis to explore potential mediators between different clusters and all-cause mortality.
RESULTS RESULTS
A total of 1756 patients were included (mean age 51.2, SD 13.0; 60.3% female), with a median follow-up of 5.7 years. Three clusters were identified: Cluster 1 (n = 543) was characterised by overweight/obesity (body mass index ≥ 25 kg/m
CONCLUSION CONCLUSIONS
Overweight/obesity older patients with more comorbidities had the highest risk of long-term all-cause mortality, and in the young group population overweight/obesity insignificantly increased the risk in the long-term follow-up, providing a basis for stratified phenotypic risk management.

Identifiants

pubmed: 38850064
doi: 10.1111/eci.14261
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e14261

Informations de copyright

© 2024 The Author(s). European Journal of Clinical Investigation published by John Wiley & Sons Ltd on behalf of Stichting European Society for Clinical Investigation Journal Foundation.

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Auteurs

Yang Chen (Y)

Liverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University, Liverpool Heart and Chest Hospital, Liverpool, UK.

Ying Gue (Y)

Liverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University, Liverpool Heart and Chest Hospital, Liverpool, UK.

Maciej Banach (M)

Ciccarone Center for the Prevention of Cardiovascular Disease, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Department of Preventive Cardiology and Lipidology, Medical University of Lodz, Lodz, Poland.
Department of Cardiology and Adult Congenital Heart Diseases, Polish Mother's Memorial Hospital Research Institute (PMMHRI), Lodz, Poland.
Cardiovascular Research Centre, University of Zielona Gora, Zielona Gora, Poland.

Dimitri Mikhailidis (D)

Department of Clinical Biochemistry, Royal Free Hospital Campus, University College London Medical School, University College London (UCL), London, UK.

Peter P Toth (PP)

Ciccarone Center for the Prevention of Cardiovascular Disease, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Department of Preventive Cardiology, CGH Medical Center, Sterling, Illinois, USA.

Marek Gierlotka (M)

Department of Cardiology, Institute of Medical Sciences, University of Opole, Opole, Poland.

Tadeusz Osadnik (T)

Faculty of Medical Sciences in Zabrze, Department of Pharmacology, Medical University of Silesia, Zabrze, Poland.

Marcin Golawski (M)

Faculty of Medical Sciences in Zabrze, Department of Pharmacology, Medical University of Silesia, Zabrze, Poland.

Tomasz Tomasik (T)

Department of Family Medicine, Jagiellonian University Medical College, Kraków, Poland.

Adam Windak (A)

Department of Family Medicine, Jagiellonian University Medical College, Kraków, Poland.

Jacek Jozwiak (J)

Department of Family Medicine and Public Health, Institute of Medical Sciences, University of Opole, Opole, Poland.

Gregory Y H Lip (GYH)

Liverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University, Liverpool Heart and Chest Hospital, Liverpool, UK.
Danish Centre for Health Services Research, Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.

Classifications MeSH