Cargando…
Effects of RAS inhibitors on all-site cancers and mortality in the Hong Kong diabetes surveillance database (2002-2019)
BACKGROUND: Cancer is replacing cardiovascular-disease as a leading cause of death in type 2 diabetes (T2D). The association of RAS-inhibitors (RASi) and cancer, including differences between angiotensin-converting-enzyme-inhibitor (ACEi) and angiotensin-receptor-blocker (ARBs) as well as their asso...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9399959/ https://www.ncbi.nlm.nih.gov/pubmed/35970023 http://dx.doi.org/10.1016/j.ebiom.2022.104219 |
_version_ | 1784772644353081344 |
---|---|
author | Yang, Aimin Wu, Hongjiang Lau, Eric S.H. Shi, Mai Fan, Baoqi Kong, Alice Pik-Shan Ma, Ronald Ching-Wan Luk, Andrea On-Yan Chan, Juliana Chung-Ngor Chow, Elaine |
author_facet | Yang, Aimin Wu, Hongjiang Lau, Eric S.H. Shi, Mai Fan, Baoqi Kong, Alice Pik-Shan Ma, Ronald Ching-Wan Luk, Andrea On-Yan Chan, Juliana Chung-Ngor Chow, Elaine |
author_sort | Yang, Aimin |
collection | PubMed |
description | BACKGROUND: Cancer is replacing cardiovascular-disease as a leading cause of death in type 2 diabetes (T2D). The association of RAS-inhibitors (RASi) and cancer, including differences between angiotensin-converting-enzyme-inhibitor (ACEi) and angiotensin-receptor-blocker (ARBs) as well as their associations independent of blood pressure lowering, remains inconclusive in T2D. METHODS: We conducted a cohort study with new-user design in 253,491 patients in the Hong-Kong-Diabetes-Surveillance-Database (HKDSD) in 2002-2019. We evaluated the associations of time-varying RASi use (ACEi and ARBs) with all-site cancer, diabetes-related cancers, and cancer-specific mortality including comparison with new-users of calcium-channel-blockers (CCBs) as an active-comparator group. FINDINGS: Of 253,491, 133,730 (52.8%) were new-RASi and 119,761 (47.2%) were non-RASi users with a median follow-up period of 6.3 (interquartile ragne: 3.4-9.2) years (1,678,719 patient-years). After propensity-score weighting and adjustment for time-varying covariables, RASi use was associated with lower risk of all-site cancer (HR=0.76, 95%CI: 0.74-0.79), diabetes-related cancer (HR=0.79, 95%CI: 0.75-0.84), cancer-specific mortality (HR=0.50, 95%CI: 0.47-0.53), and diabetes-related cancer mortality (HR=0.49, 95%CI: 0.45-0.54) versus non-RASi. Amongst RASi users, ARBs use was associated with lower risk of cancer-specific mortality versus ACEi (HR=0.77, 95%CI: 0.66-0.91). Use of RASi was associated with an estimated-prevention of 2.6 (95%CI: 2.3-3.0) all-site cancer per-1000-person-years and 2.2 (95%CI: 2.0-2.5) cancer-related mortality per-1000-person-years. Lower risk of cancer-specific mortality was similarly observed in new-RASi compared with new-CCBs users. INTERPRETATION: RASi use was independently associated with lower cancer risk in T2D with stronger associations in users of ARBs than ACEi. The benefits of RASi in patients with diabetes might go beyond cardiovascular-renal protection if confirmed by other real-world studies and trials. FUNDING: Dr. Aimin Yang was supported by a CUHK Impact-Research-Fellowship Scheme. |
format | Online Article Text |
id | pubmed-9399959 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-93999592022-08-25 Effects of RAS inhibitors on all-site cancers and mortality in the Hong Kong diabetes surveillance database (2002-2019) Yang, Aimin Wu, Hongjiang Lau, Eric S.H. Shi, Mai Fan, Baoqi Kong, Alice Pik-Shan Ma, Ronald Ching-Wan Luk, Andrea On-Yan Chan, Juliana Chung-Ngor Chow, Elaine eBioMedicine Articles BACKGROUND: Cancer is replacing cardiovascular-disease as a leading cause of death in type 2 diabetes (T2D). The association of RAS-inhibitors (RASi) and cancer, including differences between angiotensin-converting-enzyme-inhibitor (ACEi) and angiotensin-receptor-blocker (ARBs) as well as their associations independent of blood pressure lowering, remains inconclusive in T2D. METHODS: We conducted a cohort study with new-user design in 253,491 patients in the Hong-Kong-Diabetes-Surveillance-Database (HKDSD) in 2002-2019. We evaluated the associations of time-varying RASi use (ACEi and ARBs) with all-site cancer, diabetes-related cancers, and cancer-specific mortality including comparison with new-users of calcium-channel-blockers (CCBs) as an active-comparator group. FINDINGS: Of 253,491, 133,730 (52.8%) were new-RASi and 119,761 (47.2%) were non-RASi users with a median follow-up period of 6.3 (interquartile ragne: 3.4-9.2) years (1,678,719 patient-years). After propensity-score weighting and adjustment for time-varying covariables, RASi use was associated with lower risk of all-site cancer (HR=0.76, 95%CI: 0.74-0.79), diabetes-related cancer (HR=0.79, 95%CI: 0.75-0.84), cancer-specific mortality (HR=0.50, 95%CI: 0.47-0.53), and diabetes-related cancer mortality (HR=0.49, 95%CI: 0.45-0.54) versus non-RASi. Amongst RASi users, ARBs use was associated with lower risk of cancer-specific mortality versus ACEi (HR=0.77, 95%CI: 0.66-0.91). Use of RASi was associated with an estimated-prevention of 2.6 (95%CI: 2.3-3.0) all-site cancer per-1000-person-years and 2.2 (95%CI: 2.0-2.5) cancer-related mortality per-1000-person-years. Lower risk of cancer-specific mortality was similarly observed in new-RASi compared with new-CCBs users. INTERPRETATION: RASi use was independently associated with lower cancer risk in T2D with stronger associations in users of ARBs than ACEi. The benefits of RASi in patients with diabetes might go beyond cardiovascular-renal protection if confirmed by other real-world studies and trials. FUNDING: Dr. Aimin Yang was supported by a CUHK Impact-Research-Fellowship Scheme. Elsevier 2022-08-12 /pmc/articles/PMC9399959/ /pubmed/35970023 http://dx.doi.org/10.1016/j.ebiom.2022.104219 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Articles Yang, Aimin Wu, Hongjiang Lau, Eric S.H. Shi, Mai Fan, Baoqi Kong, Alice Pik-Shan Ma, Ronald Ching-Wan Luk, Andrea On-Yan Chan, Juliana Chung-Ngor Chow, Elaine Effects of RAS inhibitors on all-site cancers and mortality in the Hong Kong diabetes surveillance database (2002-2019) |
title | Effects of RAS inhibitors on all-site cancers and mortality in the Hong Kong diabetes surveillance database (2002-2019) |
title_full | Effects of RAS inhibitors on all-site cancers and mortality in the Hong Kong diabetes surveillance database (2002-2019) |
title_fullStr | Effects of RAS inhibitors on all-site cancers and mortality in the Hong Kong diabetes surveillance database (2002-2019) |
title_full_unstemmed | Effects of RAS inhibitors on all-site cancers and mortality in the Hong Kong diabetes surveillance database (2002-2019) |
title_short | Effects of RAS inhibitors on all-site cancers and mortality in the Hong Kong diabetes surveillance database (2002-2019) |
title_sort | effects of ras inhibitors on all-site cancers and mortality in the hong kong diabetes surveillance database (2002-2019) |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9399959/ https://www.ncbi.nlm.nih.gov/pubmed/35970023 http://dx.doi.org/10.1016/j.ebiom.2022.104219 |
work_keys_str_mv | AT yangaimin effectsofrasinhibitorsonallsitecancersandmortalityinthehongkongdiabetessurveillancedatabase20022019 AT wuhongjiang effectsofrasinhibitorsonallsitecancersandmortalityinthehongkongdiabetessurveillancedatabase20022019 AT lauericsh effectsofrasinhibitorsonallsitecancersandmortalityinthehongkongdiabetessurveillancedatabase20022019 AT shimai effectsofrasinhibitorsonallsitecancersandmortalityinthehongkongdiabetessurveillancedatabase20022019 AT fanbaoqi effectsofrasinhibitorsonallsitecancersandmortalityinthehongkongdiabetessurveillancedatabase20022019 AT kongalicepikshan effectsofrasinhibitorsonallsitecancersandmortalityinthehongkongdiabetessurveillancedatabase20022019 AT maronaldchingwan effectsofrasinhibitorsonallsitecancersandmortalityinthehongkongdiabetessurveillancedatabase20022019 AT lukandreaonyan effectsofrasinhibitorsonallsitecancersandmortalityinthehongkongdiabetessurveillancedatabase20022019 AT chanjulianachungngor effectsofrasinhibitorsonallsitecancersandmortalityinthehongkongdiabetessurveillancedatabase20022019 AT chowelaine effectsofrasinhibitorsonallsitecancersandmortalityinthehongkongdiabetessurveillancedatabase20022019 |