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| DOI | 10.1186/S12916-025-03915-4 | ||||
| Año | 2025 | ||||
| Tipo | artículo de investigación |
Citas Totales
Autores Afiliación Chile
Instituciones Chile
% Participación
Internacional
Autores
Afiliación Extranjera
Instituciones
Extranjeras
BackgroundAssociations of anxiety disorder and depression with coronary artery disease (CAD) are heterogeneous between populations. This study investigated how genetic susceptibility to CAD alters these associations with incident CAD, comparing and combining anxiety disorder and depression.MethodsThis is a prospective cohort study using UK Biobank. Diagnoses of anxiety disorder and depression were ascertained through linked hospital admission data. Incident CAD was ascertained through hospital admission and death certificate data after baseline. CAD polygenic risk score (PRSCAD) was obtained from CARDIoGRAMplus4 and categorised into low, intermediate, and high. Cox proportional hazard models were used to examine associations between anxiety disorder and depression and CAD.ResultsBoth anxiety disorder (HR 2.31, 95% CI 1.92-2.78) and depression (HR 2.15, 95% CI 1.90-2.24) were associated with CAD after adjusting for sociodemographic confounders. There was an addictive interaction between depression and PRSCAD (RERI 0.97, 95% CI 0.12-1.81) such that the association between depression and CAD was strongest among those with a high PRSCAD whilst there was no such evidence for anxiety disorder. Anxiety disorder only (HR 1.68, 95% 1.16-2.44), depression only (HR 2.13, 95% CI 1.72-2.64), and concomitant anxiety disorder and depression (HR 3.85, 95% CI 2.48-5.98) were associated with CAD even among people with a low PRSCAD. Adjusting for potential mediators attenuated all these associations across PRS categories.ConclusionsCAD genetic susceptibility might partly contribute to the clustering of depression and CAD but does not provide a full explanation, nor does it explain the association between anxiety disorder and CAD. Therefore, other mechanisms should be explored.
| Ord. | Autor | Género | Institución - País |
|---|---|---|---|
| 1 | Nakada, Shinya | Hombre |
Univ Glasgow - Reino Unido
University of Glasgow - Reino Unido |
| 2 | Ward, Joey | - |
Univ Glasgow - Reino Unido
University of Glasgow - Reino Unido |
| 3 | Strawbridge, Rona J. | - |
Univ Glasgow - Reino Unido
Karolinska Inst - Suecia HDR UK - Reino Unido University of Glasgow - Reino Unido Karolinska Institutet - Suecia Health Data Research UK - Reino Unido |
| 4 | Welsh, Paul | - |
Univ Glasgow - Reino Unido
University of Glasgow - Reino Unido |
| 5 | Celis-Morales, Carlos | - |
Univ Glasgow - Reino Unido
Universidad Católica del Maule - Chile Universidad Arturo Prat - Chile University of Glasgow - Reino Unido |
| 6 | Ho, Frederick K. | - |
Univ Glasgow - Reino Unido
University of Glasgow - Reino Unido |
| 7 | Pell, Jill P. | - |
Univ Glasgow - Reino Unido
University of Glasgow - Reino Unido |
| Fuente |
|---|
| Medical Research Council |
| Wellcome Trust |
| British Heart Foundation |
| Northwest Regional Development Agency |
| Scottish Government |
| Department of Health |
| University of Edinburgh |
| University of Glasgow |
| Welsh Assembly government |
| Medical Research Council, Department of Health, Scottish Government |
| National Health Service |
| University of Edinburgh/University of Glasgow |
| British Heart Foundation - Medical Research Council |
| UKB |
| Agradecimiento |
|---|
| We thank all participants and staff of UK Biobank. This work uses data provided by patients and collected by the National Health Service as part of their care and support. The UKB (UK Biobank) was established by the Wellcome Trust, Medical Research Council, Department of Health, Scottish Government, and Northwest Regional Development Agency. UKB has also had funding from the Welsh Assembly Government and the British Heart Foundation. Data collection was funded by UKB. We are also grateful to the Medical Research Council and the University of Edinburgh/University of Glasgow. This work was supported by the Medical Research Council (MR/N013166/1-LGH/MS/MED2525). |
| S.N. is supported by a Ph.D. studentship award from the Medical Research Council (MR/N013166/1-LGH/MS/MED2525). |
| S.N. is supported by a Ph.D. studentship award from the Medical Research Council (MR/N013166/1-LGH/MS/MED2525). |