Evaluating different low‐density lipoprotein cholesterol thresholds to initiate statin for prevention of cardiovascular diseases in patients with type 2 diabetes mellitus: A target trial emulation study

Author:

Wan Eric Yuk Fai123ORCID,Xu Wanchun1,Mok Anna Hoi Ying1,Chin Weng Yee1,Yu Esther Yee Tak1,Chui Celine Sze Ling345,Chan Esther Wai Yin23,Wong Ian Chi Kei236,Lam Cindy Lo Kuen1,Danaei Goodarz78

Affiliation:

1. Department of Family Medicine and Primary Care Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region China

2. Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region China

3. Laboratory of Data Discovery for Health (D24H) Hong Kong Science and Technology Park, Sha Tin, Hong Kong Special Administrative Region China

4. School of Nursing, Li Ka Shing Faculty of Medicine The University of Hong Kong, Hong Kong Special Administrative Region China

5. School of Public Health, Li Ka Shing Faculty of Medicine The University of Hong Kong, Hong Kong Special Administrative Region China

6. Research Department of Practice and Policy School of Pharmacy, University College London London United Kingdom

7. Department of Global Health and Population Harvard TH Chan School of Public Health Boston Massachusetts USA

8. Department of Epidemiology Harvard TH Chan School of Public Health Boston Massachusetts USA

Abstract

AbstractAimThe present study aimed to evaluate the effect of statin therapy for primary prevention of cardiovascular diseases (CVDs) when initiating therapy at different baseline low‐density lipoprotein cholesterol (LDL‐C) levels in patients with type 2 diabetes mellitus (T2DM).Materials and MethodsUsing territory‐wide public electronic medical records in Hong Kong, we emulated a sequence of trials on patients with T2DM with elevated LDL‐C levels in every calendar month from January 2008 to December 2014. Pooled logistic regression was applied to obtain the hazard ratios for the major CVDs (stroke, myocardial infarction, heart failure), all‐cause mortality and major adverse events (myopathies and liver dysfunction) of statin therapy.ResultsThe estimated hazard ratios (95% confidence intervals) of CVD incidence for statin initiation were 0.78 (0.72, 0.84) in patients with baseline LDL‐C of 1.8‐2.5 mmol/L (i.e., 70‐99 mg/dL) and 0.90 (0.88, 0.92) in patients with baseline LDL‐C ≥2.6 mmol/L (i.e., ≥100 mg/dL) in intention‐to‐treat analysis, which was 0.59 (0.51, 0.68) and 0.77 (0.74, 0.81) in per‐protocol analysis, respectively. No significant increased risks were observed for the major adverse events. The absolute 10‐year risk difference of overall CVD in per‐protocol analysis was −7.1% (−10.7%, −3.6%) and −3.9% (−5.1%, −2.7%) in patients with baseline LDL‐C 1.8‐2.5 and ≥2.6 mmol/L, respectively. The effectiveness and safety were consistently observed in patients aged >75 years initiating statin at both LDL‐C thresholds.ConclusionsCompared with the threshold of 2.6 mmol/L, initiating statin in patients with a lower baseline LDL‐C level at 1.8‐2.5 mmol/L can further reduce the risks of CVD and all‐cause mortality without significantly increasing the risk of major adverse events in patients with T2DM, including patients aged >75 years.

Funder

Health Bureau

Publisher

Wiley

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