TY - JOUR
T1 - Association Between Triglycerides and Residual Cardiovascular Risk in Patients With Type 2 Diabetes Mellitus and Established Cardiovascular Disease (From the Bypass Angioplasty Revascularization Investigation 2 Diabetes [BARI 2D] Trial)
AU - Nelson, Adam J.
AU - Navar, Ann Marie
AU - Mulder, Hillary
AU - Wojdyla, Daniel
AU - Philip, Sephy
AU - Granowitz, Craig
AU - Peterson, Eric D.
AU - Pagidipati, Neha J.
N1 - Funding Information:
AJN - Grants from Diabetes Australia and the Royal Australasian College of Physicians; AMN - Grants from Regeneron and Sanofi during the conduct of the study; additional research grants to her institution from Regeneron, Sanofi, Amgen, Janssen, and Amarin during the conduct of the study outside of the submitted work; and personal fees from Regeneron, Sanofi, Amgen, Astra Zeneca, NovoNordisk, and Amarin outside of the submitted work; SP - Employee of Amarin Pharma, Inc.; CG - Employee of Amarin Pharma, Inc. EDP - Grants and personal fees from Sanofi and grants from Regeneron during conduct of study as well as grants and personal fees from AstraZeneca, Amgen, and Merck outside of the submitted work. NJP - Grants from Amgen, Regeneron Pharmaceuticals, Sanofi-Aventis, and Verily Life Sciences. HM, DW - both have nothing to declare.
Funding Information:
This analysis was funded by Amarin Pharma, Inc. BARI-2D was funded by the National Heart, Lung and Blood Institute and the National Institute of Diabetes and Digestive and Kidney Diseases ; as well as multiple other private sources of funding ( GlaxoSmithKline , Lantheus Medical Imaging , Astellas Pharma , Merck , Abbott Laboratories , Pfizer , MediSense , Bayer , Becton Dickinson , J.R. Carlson Labs , Centocor , Eli Lilly , LipoScience , Novartis , and Novo Nordisk ).
Publisher Copyright:
© 2020 The Authors
PY - 2020/10/1
Y1 - 2020/10/1
N2 - Triglyceride (TG) levels encompass several lipoproteins that have been implicated in atherogenic pathways. Whether TG levels independently associate with cardiovascular disease both overall and, in particular among patients with established coronary artery disease (CAD) and type 2 diabetes (T2DM), remains controversial. Data from the Bypass Angioplasty Revascularization Investigation 2 Diabetes (BARI 2D) trial was used to evaluate patients with T2DM and CAD. Cox proportional hazards models were used to determine the association between TG levels and outcomes. Stepwise adjustment was performed for demographics, clinical factors, lipid profile and statin treatment. The primary composite outcome was time to CV death, myocardial infarction (MI), or stroke and secondary outcome was CV death. Among 2,307 patients with T2DM and CAD, the mean (±SD) TG levels were 181 (±136) with a median (Q1–Q3) 148mg/dL (104–219). Overall, 51% of patients had TG <150 mg/dL, 18% 150–199 mg/dL, 28% 200–499 mg/dL and 3% ≥500 mg/dL. Participants with elevated TG levels (≥150 mg/dL) were younger (61 vs 63 years, p <0.001), had higher BMI (32 vs 30 kg/m2, p <0.001), more likely to have had prior MI (34.2 vs 30.1%, p = 0.033) and revascularization (25.8 vs 21.4%, p = 0.013), had lower HDL-C (34 vs 39 mg/dL, p <0.001) and higher HbA1c (8 vs 7%, p <0.001). In unadjusted analyses, baseline TG levels were linearly associated with both the primary composite and secondary outcomes. In fully adjusted analyses, every 50 mg/dL increase in TG level was associated with a 3.8% (HR 1.038, 95%CI 1.004–1.072, p <0.001) increase in the primary composite outcome and a 6.4% (HR 1.064 95%CI 1.018–1.113, p <0.001) increase in the secondary outcome. There was no interaction between TG and outcomes within key subgroups including female sex, additional non-coronary atherosclerotic disease, CKD or low LDL (<100 mg/dL). In conclusion, among patients with T2DM and CAD, elevated TG were independently associated with adverse cardiovascular outcomes, even after adjustment for clinical and simple biochemical covariates.
AB - Triglyceride (TG) levels encompass several lipoproteins that have been implicated in atherogenic pathways. Whether TG levels independently associate with cardiovascular disease both overall and, in particular among patients with established coronary artery disease (CAD) and type 2 diabetes (T2DM), remains controversial. Data from the Bypass Angioplasty Revascularization Investigation 2 Diabetes (BARI 2D) trial was used to evaluate patients with T2DM and CAD. Cox proportional hazards models were used to determine the association between TG levels and outcomes. Stepwise adjustment was performed for demographics, clinical factors, lipid profile and statin treatment. The primary composite outcome was time to CV death, myocardial infarction (MI), or stroke and secondary outcome was CV death. Among 2,307 patients with T2DM and CAD, the mean (±SD) TG levels were 181 (±136) with a median (Q1–Q3) 148mg/dL (104–219). Overall, 51% of patients had TG <150 mg/dL, 18% 150–199 mg/dL, 28% 200–499 mg/dL and 3% ≥500 mg/dL. Participants with elevated TG levels (≥150 mg/dL) were younger (61 vs 63 years, p <0.001), had higher BMI (32 vs 30 kg/m2, p <0.001), more likely to have had prior MI (34.2 vs 30.1%, p = 0.033) and revascularization (25.8 vs 21.4%, p = 0.013), had lower HDL-C (34 vs 39 mg/dL, p <0.001) and higher HbA1c (8 vs 7%, p <0.001). In unadjusted analyses, baseline TG levels were linearly associated with both the primary composite and secondary outcomes. In fully adjusted analyses, every 50 mg/dL increase in TG level was associated with a 3.8% (HR 1.038, 95%CI 1.004–1.072, p <0.001) increase in the primary composite outcome and a 6.4% (HR 1.064 95%CI 1.018–1.113, p <0.001) increase in the secondary outcome. There was no interaction between TG and outcomes within key subgroups including female sex, additional non-coronary atherosclerotic disease, CKD or low LDL (<100 mg/dL). In conclusion, among patients with T2DM and CAD, elevated TG were independently associated with adverse cardiovascular outcomes, even after adjustment for clinical and simple biochemical covariates.
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U2 - 10.1016/j.amjcard.2020.07.005
DO - 10.1016/j.amjcard.2020.07.005
M3 - Article
C2 - 32773223
AN - SCOPUS:85089141224
SN - 0002-9149
VL - 132
SP - 36
EP - 43
JO - American Journal of Cardiology
JF - American Journal of Cardiology
ER -