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- Publisher Website: 10.1007/s00125-014-3458-7
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Article: The relationship of fibroblast growth factor 21 with cardiovascular outcome events in the Fenofibrate Intervention and Event Lowering in Diabetes study
Title | The relationship of fibroblast growth factor 21 with cardiovascular outcome events in the Fenofibrate Intervention and Event Lowering in Diabetes study |
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Authors | |
Keywords | Cardiovascular outcome Fenofibrate Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study Fibroblast growth factor 21 |
Issue Date | 2015 |
Citation | Diabetologia, 2015, v. 58 n. 3, p. 464-473 How to Cite? |
Abstract | AIMS/HYPOTHESIS: Circulating fibroblast growth factor 21 (FGF21) levels are often elevated in obesity, dyslipidaemia, insulin resistance and type 2 diabetes. This study investigated the relationship of plasma FGF21 levels with cardiovascular events in patients with type 2 diabetes. METHODS: Plasma FGF21 levels were measured by ELISA at baseline in 9,697 individuals with type 2 diabetes participating in the Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study. We assessed the association of FGF21 levels with the incidence of different cardiovascular outcomes over 5 years. The primary outcome was total cardiovascular disease (CVD) events and the secondary outcomes were the four individual components: coronary heart disease events, total stroke, CVD mortality and coronary and carotid revascularisation. The tertiary outcome was hospitalisation for angina pectoris. RESULTS: Higher baseline FGF21 levels were associated with higher risks of all cardiovascular outcome events after adjusting for the study treatment allocation (all p < 0.01). The associations remained significant for total CVD events and for coronary and carotid revascularisation after further adjusting for confounding factors, with the HR (95% CI) being 1.28 (1.10, 1.50) and 1.26 (1.01, 1.56), respectively, for the highest tertile compared with the lowest tertile (overall effect p = 0.002 and 0.007, respectively). The addition of FGF21 levels to a model including established CVD risk factors predicting total CVD events led to a non-significant increase in the C-statistic but there was a significant improvement in integrated discrimination and net reclassification. CONCLUSIONS/INTERPRETATION: Higher baseline plasma FGF21 levels were associated with higher risk of cardiovascular events in patients with type 2 diabetes. |
Persistent Identifier | http://hdl.handle.net/10722/214322 |
ISSN | 2023 Impact Factor: 8.4 2023 SCImago Journal Rankings: 3.355 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Ong, KL | - |
dc.contributor.author | Januszewski, AS | - |
dc.contributor.author | O’Connell, R | - |
dc.contributor.author | Jenkins, AJ | - |
dc.contributor.author | Xu, A | - |
dc.contributor.author | Sullivan, DR | - |
dc.contributor.author | Barter, PJ | - |
dc.contributor.author | Hung, WT | - |
dc.contributor.author | Scott, RS | - |
dc.contributor.author | Taskinen, MR | - |
dc.date.accessioned | 2015-08-21T11:13:44Z | - |
dc.date.available | 2015-08-21T11:13:44Z | - |
dc.date.issued | 2015 | - |
dc.identifier.citation | Diabetologia, 2015, v. 58 n. 3, p. 464-473 | - |
dc.identifier.issn | 0012-186X | - |
dc.identifier.uri | http://hdl.handle.net/10722/214322 | - |
dc.description.abstract | AIMS/HYPOTHESIS: Circulating fibroblast growth factor 21 (FGF21) levels are often elevated in obesity, dyslipidaemia, insulin resistance and type 2 diabetes. This study investigated the relationship of plasma FGF21 levels with cardiovascular events in patients with type 2 diabetes. METHODS: Plasma FGF21 levels were measured by ELISA at baseline in 9,697 individuals with type 2 diabetes participating in the Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study. We assessed the association of FGF21 levels with the incidence of different cardiovascular outcomes over 5 years. The primary outcome was total cardiovascular disease (CVD) events and the secondary outcomes were the four individual components: coronary heart disease events, total stroke, CVD mortality and coronary and carotid revascularisation. The tertiary outcome was hospitalisation for angina pectoris. RESULTS: Higher baseline FGF21 levels were associated with higher risks of all cardiovascular outcome events after adjusting for the study treatment allocation (all p < 0.01). The associations remained significant for total CVD events and for coronary and carotid revascularisation after further adjusting for confounding factors, with the HR (95% CI) being 1.28 (1.10, 1.50) and 1.26 (1.01, 1.56), respectively, for the highest tertile compared with the lowest tertile (overall effect p = 0.002 and 0.007, respectively). The addition of FGF21 levels to a model including established CVD risk factors predicting total CVD events led to a non-significant increase in the C-statistic but there was a significant improvement in integrated discrimination and net reclassification. CONCLUSIONS/INTERPRETATION: Higher baseline plasma FGF21 levels were associated with higher risk of cardiovascular events in patients with type 2 diabetes. | - |
dc.language | eng | - |
dc.relation.ispartof | Diabetologia | - |
dc.subject | Cardiovascular outcome | - |
dc.subject | Fenofibrate | - |
dc.subject | Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study | - |
dc.subject | Fibroblast growth factor 21 | - |
dc.title | The relationship of fibroblast growth factor 21 with cardiovascular outcome events in the Fenofibrate Intervention and Event Lowering in Diabetes study | - |
dc.type | Article | - |
dc.identifier.email | Xu, A: amxu@hkucc.hku.hk | - |
dc.identifier.authority | Xu, A=rp00485 | - |
dc.identifier.doi | 10.1007/s00125-014-3458-7 | - |
dc.identifier.scopus | eid_2-s2.0-84925486838 | - |
dc.identifier.hkuros | 246866 | - |
dc.identifier.volume | 58 | - |
dc.identifier.issue | 3 | - |
dc.identifier.spage | 464 | - |
dc.identifier.epage | 473 | - |
dc.identifier.eissn | 1432-0428 | - |
dc.identifier.isi | WOS:000349244100007 | - |
dc.identifier.issnl | 0012-186X | - |