Pioglitazone, SGLT2 inhibitors and their combination for primary prevention of cardiovascular disease and heart failure in type 2 diabetes: Real-world evidence from a nationwide cohort database

被引:7
|
作者
Lo, Shih-Chang [1 ,2 ]
Kornelius, Edy [2 ,3 ]
Liao, Pei-Lun [4 ]
Huang, Jing-Yang [1 ,4 ]
Yang, Yi-Sun [2 ,3 ,5 ]
Huang, Chien-Ning [1 ,2 ,3 ,6 ]
机构
[1] Chung Shan Med Univ, Inst Med, Taichung, Taiwan
[2] Chung Shan Med Univ Hosp, Dept Internal Med, Div Endocrinol & Metab, Taichung, Taiwan
[3] Chung Shan Med Univ, Sch Med, Taichung, Taiwan
[4] Chung Shan Med Univ Hosp, Dept Med Res, Taichung, Taiwan
[5] Chung Shan Med Univ, Sch Med, 110th 1 Sect,Jian Guo North Rd, Taichung, Taiwan
[6] Chung Shan Med Univ, Inst Med, 110th 1st Sect,Jian Guo North Rd, Taichung, Taiwan
关键词
Type; 2; diabetes; Cardiovascular disease; SGLT2; inhibitors; Thiazolidinedione; RISK; THIAZOLIDINEDIONES; EMPAGLIFLOZIN; METFORMIN; MELLITUS; OUTCOMES; EVENTS; WEIGHT;
D O I
10.1016/j.diabres.2023.110685
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To evaluate the effect of SGLT2is, pioglitazone, and their combination on the risk of major adverse cardiovascular events (MACE) and heart failure in type 2 diabetes mellitus (T2DM) patients without a history of cardiovascular disease.Research design and methods: Using Taiwan National Health Insurance Research Database, we identified four groups based on medication use, including 1) both SGLT2is and pioglitazone, 2) SGLT2i, 3) pioglitazone and 4) non-study drugs (reference group). The four groups were matched by propensity score. The primary outcome was 3-point MACE, which included myocardial infarction, stroke, cardiovascular death, and the secondary outcome was incidence of heart failure.Results: After propensity-matching, each group included 15,601 patients. Compared with the reference group, the pioglitazone/SGLT2i combination group had a significantly lower risk for MACE (aHR 0.76, 95 % CI 0.66-0.88) and heart failure (aHR 0.67, 95 % CI 0.55-0.82). Pioglitazone was associated with a lower risk of MACE (aHR 0.82, 95 % CI 0.71-0.94) and there was no difference in risk of heart failure compared with the reference group. The incidence of heart failure was significantly decreased in the SGLT2i group (aHR 0.7, 95 % CI 0.58-0.86).Conclusion: Combination therapy with pioglitazone and SGLT2is is an effective treatment in the primary prevention of MACE and heart failure in patients with type 2 diabetes.
引用
收藏
页数:7
相关论文
共 50 条
  • [41] Real-world comparison of hospitalization costs for heart failure in type 2 diabetes mellitus patients with established cardiovascular disease treated with canagliflozin versus other antihyperglycemic agents
    Chen, Yen-Wen
    Voelker, Jennifer
    Tunceli, Ozgur
    Pericone, Christopher D.
    Bookhart, Brahim
    Durkin, Michael
    JOURNAL OF MEDICAL ECONOMICS, 2020, 23 (04) : 401 - 406
  • [42] SGLT2 Inhibitors in Type 2 Diabetes Mellitus and Heart Failure-A Concise Review
    Keller, Daria M.
    Ahmed, Natasha
    Tariq, Hamza
    Walgamage, Malsha
    Walgamage, Thilini
    Mohammed, Azad
    Chou, Jadzia Tin-Tsen
    Kaluzna-Oleksy, Marta
    Lesiak, Maciej
    Straburzynska-Migaj, Ewa
    JOURNAL OF CLINICAL MEDICINE, 2022, 11 (06)
  • [43] Cardiovascular and renal outcomes among patients with type 2 diabetes using SGLT2 inhibitors added to metformin: a population-based cohort study from the UK
    Gonzalez Perez, Antonio
    Vizcaya, David
    Saez, Maria E.
    Lind, Marcus
    Garcia Rodriguez, Luis A.
    BMJ OPEN DIABETES RESEARCH & CARE, 2023, 11 (01)
  • [44] Nephroprotective effect of SGLT2 inhibitors in elderly patients with type 2 diabetes mellitus and hypertension: a real-world population-based cohort study
    Geng, Shasha
    Li, Yang
    Ge, Jianli
    Liu, Yue
    Li, Qingqing
    Chen, Xin
    Zhu, Yingqian
    Guo, Xiaotong
    Yuan, Huixiao
    Wang, Xiaoli
    Jiang, Hua
    POSTGRADUATE MEDICINE, 2024, 136 (08) : 855 - 863
  • [45] Barriers to initiating SGLT2 inhibitors in diabetic kidney disease: a real-world study
    Jeong, Su Jin
    Lee, Seung Eun
    Shin, Dong Hyun
    Park, Ie Byung
    Lee, Hui Seung
    Kim, Kyoung-Ah
    BMC NEPHROLOGY, 2021, 22 (01)
  • [46] Use of i-SGLT2 in patients with type 2 Diabetes Mellitus, cardiovascular disease and heart failure: what evidence do we have available?
    Martinez, Felipe
    Garcia Brasca, Daniela F.
    REVISTA DE LA FEDERACION ARGENTINA DE CARDIOLOGIA, 2020, 49 : 19 - 23
  • [47] Efficacy, renal safety and tolerability of sodium-glucose cotransporter 2 inhibitors (SGLT2i) in elderly patients with type 2 diabetes: A real-world experience
    Tumminia, Andrea
    Graziano, Marco
    Vinciguerra, Federica
    Lomonaco, Andrea
    Frittita, Lucia
    PRIMARY CARE DIABETES, 2021, 15 (02) : 283 - 288
  • [48] Comparative cardiovascular benefits of individual SGLT2 inhibitors in type 2 diabetes and heart failure: a systematic review and network meta-analysis of randomized controlled trials
    Kongmalai, Tanawan
    Hadnorntun, Phorntida
    Leelahavarong, Pattara
    Kongmalai, Pinkawas
    Srinonprasert, Varalak
    Chirakarnjanakorn, Srisakul
    Chaikledkaew, Usa
    McKay, Gareth
    Attia, John
    Thakkinstian, Ammarin
    FRONTIERS IN ENDOCRINOLOGY, 2023, 14
  • [49] Comparing cardiovascular benefits between GLP-1 receptor agonists and SGLT2 inhibitors as an add-on to metformin among patients with type 2 diabetes: A retrospective cohort study
    DeRemer, Christina E.
    Vouri, Scott M.
    Guo, Jingchuan
    Donahoo, William T.
    Winterstein, Almut G.
    Shao, Hui
    JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2021, 35 (09)
  • [50] A real-world comparison of cardiovascular, medical and costs outcomes in new users of SGLT2 inhibitors versus GLP-1 agonists
    Poonawalla, Insiya B.
    Bowe, Andy T.
    Tindal, Michael C.
    Meah, Yunus A.
    Schwab, Phil
    DIABETES RESEARCH AND CLINICAL PRACTICE, 2021, 175