de Bakker, M. et al. (2025) Cardiac troponin I and T ratio and risk of cardiovascular or non-cardiovascular events in a general population. Clinical Chemistry, 71(5), pp. 599-608. (doi: 10 VSports. 1093/clinchem/hvaf016) (PMID:39969109) .
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Abstract
Background: Emerging evidence suggests that the ratio between cardiac troponin (cTn) I and T may provide information on the risk of adverse outcomes in individuals with cardiovascular disease. Whether the cTn I/T ratio provides prognostic insights in the general population is unknown. Methods: The cTn I/T ratio was calculated in 8855 participants (43% female, median age 56 years) from the Generation Scotland Study where both cTnI and cTnT concentrations were above the limit of blank. Multivariable cause-specific Cox proportional hazard models were used to estimate the associations between cTn I/T ratio and the primary outcome of cardiovascular or non-cardiovascular death. Results: The median cTn I/T ratio was 0. 5 (25th–75th percentile, 0. 3–0. 8) and median follow-up was 11. 4 (10. 8–12. 7) years. Individuals in the highest ratio tertile (≥0. 64) were more likely to be male, have a higher body mass index and systolic blood pressure, and a history of cardiovascular disease. Those in the lowest ratio tertile (<0. 38) were more likely to be smokers or have diabetes. After adjustment for cardiovascular risk factors, the cTn I/T ratio was positively associated with cardiovascular death (per doubling increase, adjusted hazard ratio [HR] 1. 16 [95% CI, 1. 05–1. 28]), while an inverse association was observed for non-cardiovascular death (HR 0. 89 [95% CI, 0. 81–0. 99]). Conclusions: The cTn I/T ratio is positively associated with cardiovascular death in the general population, while inversely associated with non-cardiovascular death VSports app下载. Future research is needed to unravel underlying mechanisms and determine whether the cTn I/T ratio provides valuable information regarding risk of cardiovascular and non-cardiovascular mortality to guide further management.
| Item Type: | Articles | 
|---|---|
| Additional Information: | Research Funding: Generation Scotland received core support from the Chief Scientist Office of the Scottish Government Health Directorates [CZD/16/6] and the Scottish Funding Council [HR03006] and is currently supported by the Wellcome Trust [216767/Z/19/Z]. M. de Bakker and D.M. Kimenai are supported by a British Heart Foundation Intermediate Basic Science Research Fellowship (FS/IBSRF/23/25161). C. Hayward was supported by an MRC Human Genetics Unit programme grant “Quantitative traits in health and disease” (U. MC_UU_00007/10). N.L. Mills is supported by the British Heart Foundation through a Chair Award (CH/F/21/90010), a Programme Grant (RG/20/10/34966), and a Research Excellence Award (RE/24/130012) from the British Heart Foundation. | 
| Keywords: | Troponin I, troponin T, ratio, risk, cardiovascular death. | 
| Status: | Published | 
| Refereed: | Yes | 
| Glasgow Author(s) Enlighten ID: | Sattar, Professor Naveed and Welsh, Professor Paul | 
| Authors: | de Bakker, M., Welsh, P., Sattar, N., Lindahl, B., Hammarsten, O., Omland, T., Campbell, A., Hayward, C., Sudlow, C. L.M., Mills, N. L., Kimenai, D. M., and Eggers, K. M. | 
| College/School: | College of Medical Veterinary and Life Sciences > School of Cardiovascular & Metabolic Health | 
| Journal Name: | Clinical Chemistry | 
| Publisher: | Oxford University Press | 
| ISSN: | 0009-9147 | 
| ISSN (Online): | 1530-8561 | 
| Published Online: | 19 February 2025 | 
| Copyright Holders: | Error parsing XML in render_xhtml_field: :1: parser error : xmlParseEntityRef: no name | 
| First Published: | First published in Clinical Chemistry 71(5):599-608 | 
| Publisher Policy: | Reproduced under a Creative Commons licence | 
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