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Article: Galectin-3 and risk of cardiovascular events and all-cause mortality in type 2 diabetes
Title | Galectin-3 and risk of cardiovascular events and all-cause mortality in type 2 diabetes |
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Authors | |
Keywords | all-cause mortality cardiovascular outcome galectin-3 type 2 diabetes |
Issue Date | 2019 |
Publisher | John Wiley & Sons Ltd. The Journal's web site is located at http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1520-7560 |
Citation | Diabetes/Metabolism Research and Reviews, 2019, v. 35 n. 2, p. e3093 How to Cite? |
Abstract | AIMS: Recent clinical studies have shown that galectin-3 is a prognostic indicator in patients with coronary heart disease and in patients with heart failure. Experimental data suggest that galectin-3 may play a role in atherogenesis. We have evaluated whether serum galectin-3 level is associated with cardiovascular outcome in type 2 diabetes. MATERIALS AND METHODS: Galectin-3 was measured in baseline samples in 1495 persons with type 2 diabetes. The primary cardiovascular outcome, incident cardiovascular events, was defined as first non-fatal myocardial infarction, non-fatal stroke, coronary revascularization, or death from cardiovascular cause. The secondary outcome was all-cause mortality. RESULTS: At baseline, 12% of the subjects had prevalent cardiovascular disease. Serum galectin-3 was increased in the group with incident cardiovascular events compared with those who remained free of events during follow up (9.03 +/- 2.98 ng/mL vs 8.15 +/- 2.76, P < 0.01). Serum galectin-3 was also significantly increased in those subjects with a fatal outcome. The hazard ratios (HR) for cardiovascular events and all-cause mortality for individuals in the top quartile were 2.50 (95% CI 1.87, 3.36, P < 0.001) and 3.92 (95%CI 2.55, 6.01, P < 0.001), respectively. In a multivariate Cox regression analysis including traditional risk factors, log (eGFR), baseline albuminuria, and cardiovascular disease status, the HR per standard deviation change in galectin-3 was 1.13 (95% CI 1.02, 1.26, P = 0.02) for cardiovascular events and 1.17 (95% CI 1.01, 1.35, P = 0.04) for all-cause mortality. CONCLUSIONS: Serum galectin-3 is associated with adverse cardiovascular outcomes in persons with type 2 diabetes independent of traditional risk factors. |
Persistent Identifier | http://hdl.handle.net/10722/269435 |
ISSN | 2023 Impact Factor: 4.6 2023 SCImago Journal Rankings: 1.991 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Tan, KCB | - |
dc.contributor.author | Cheung, CL | - |
dc.contributor.author | Lee, CHA | - |
dc.contributor.author | Lam, JKY | - |
dc.contributor.author | Wong, Y | - |
dc.contributor.author | Shiu, SWM | - |
dc.date.accessioned | 2019-04-24T08:07:39Z | - |
dc.date.available | 2019-04-24T08:07:39Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | Diabetes/Metabolism Research and Reviews, 2019, v. 35 n. 2, p. e3093 | - |
dc.identifier.issn | 1520-7560 | - |
dc.identifier.uri | http://hdl.handle.net/10722/269435 | - |
dc.description.abstract | AIMS: Recent clinical studies have shown that galectin-3 is a prognostic indicator in patients with coronary heart disease and in patients with heart failure. Experimental data suggest that galectin-3 may play a role in atherogenesis. We have evaluated whether serum galectin-3 level is associated with cardiovascular outcome in type 2 diabetes. MATERIALS AND METHODS: Galectin-3 was measured in baseline samples in 1495 persons with type 2 diabetes. The primary cardiovascular outcome, incident cardiovascular events, was defined as first non-fatal myocardial infarction, non-fatal stroke, coronary revascularization, or death from cardiovascular cause. The secondary outcome was all-cause mortality. RESULTS: At baseline, 12% of the subjects had prevalent cardiovascular disease. Serum galectin-3 was increased in the group with incident cardiovascular events compared with those who remained free of events during follow up (9.03 +/- 2.98 ng/mL vs 8.15 +/- 2.76, P < 0.01). Serum galectin-3 was also significantly increased in those subjects with a fatal outcome. The hazard ratios (HR) for cardiovascular events and all-cause mortality for individuals in the top quartile were 2.50 (95% CI 1.87, 3.36, P < 0.001) and 3.92 (95%CI 2.55, 6.01, P < 0.001), respectively. In a multivariate Cox regression analysis including traditional risk factors, log (eGFR), baseline albuminuria, and cardiovascular disease status, the HR per standard deviation change in galectin-3 was 1.13 (95% CI 1.02, 1.26, P = 0.02) for cardiovascular events and 1.17 (95% CI 1.01, 1.35, P = 0.04) for all-cause mortality. CONCLUSIONS: Serum galectin-3 is associated with adverse cardiovascular outcomes in persons with type 2 diabetes independent of traditional risk factors. | - |
dc.language | eng | - |
dc.publisher | John Wiley & Sons Ltd. The Journal's web site is located at http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1520-7560 | - |
dc.relation.ispartof | Diabetes/Metabolism Research and Reviews | - |
dc.rights | This is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. | - |
dc.subject | all-cause mortality | - |
dc.subject | cardiovascular outcome | - |
dc.subject | galectin-3 | - |
dc.subject | type 2 diabetes | - |
dc.title | Galectin-3 and risk of cardiovascular events and all-cause mortality in type 2 diabetes | - |
dc.type | Article | - |
dc.identifier.email | Tan, KCB: kcbtan@hkucc.hku.hk | - |
dc.identifier.email | Cheung, CL: lung1212@hku.hk | - |
dc.identifier.email | Lee, CHA: achlee@hku.hk | - |
dc.identifier.email | Wong, Y: ywong@hku.hk | - |
dc.identifier.email | Shiu, SWM: swmshiu@hku.hk | - |
dc.identifier.authority | Tan, KCB=rp00402 | - |
dc.identifier.authority | Cheung, CL=rp01749 | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/dmrr.3093 | - |
dc.identifier.scopus | eid_2-s2.0-85056482604 | - |
dc.identifier.hkuros | 297361 | - |
dc.identifier.volume | 35 | - |
dc.identifier.issue | 2 | - |
dc.identifier.spage | e3093 | - |
dc.identifier.epage | e3093 | - |
dc.identifier.isi | WOS:000457591100011 | - |
dc.publisher.place | United Kingdom | - |
dc.identifier.issnl | 1520-7552 | - |