Lipid‐Lowering Therapy and Risk of Hemorrhagic Stroke: A Systematic Review and Meta‐Analysis of Randomized Controlled Trials

Author:

Bétrisey Sylvain12,Haller Moa Lina12ORCID,Efthimiou Orestis23ORCID,Speierer Alexandre12ORCID,Del Giovane Cinzia24,Moutzouri Elisavet125ORCID,Blum Manuel R.12ORCID,Aujesky Drahomir1ORCID,Rodondi Nicolas12ORCID,Gencer Baris26ORCID

Affiliation:

1. Department of General Internal Medicine, Inselspital Bern University Hospital, University of Bern Switzerland

2. Institute of Primary Health Care (BIHAM) University of Bern Switzerland

3. Institute of Social and Preventive Medicine (ISPM) University of Bern Switzerland

4. Department of Medical and Surgical Sciences for Children and Adults University Hospital of Modena and Reggio Emilia Modena MO Italy

5. Department of General Internal Medicine, Spital Emmental Burgdorf Switzerland

6. Department of Cardiology Geneva University Hospital (HUG), University of Geneva Geneva Switzerland

Abstract

Background There is debate over whether statins increase risk of hemorrhagic stroke, so we assessed current evidence, including data from new statin trials and trials of nonstatin low‐density lipoprotein‐cholesterol (LDL‐C)– and triglyceride‐lowering therapies. Methods and Results We performed a systematic review of large randomized clinical trials (≥1000 patients with ≥2 years follow‐up) of LDL‐C–lowering therapy (statin, ezetimibe, and PCSK‐9 [proprotein convertase subtilisin/kexin type 9] inhibitor) and triglyceride‐lowering therapy (omega‐3 supplements and fibrate) that reported hemorrhagic stroke as an outcome. We searched MEDLINE, Embase, and Cochrane Library up to July 2, 2021 and updated a meta‐analysis of cardiovascular statin trials published in 2012. Among our several subgroup analyses, we looked at difference depending on stroke status and also depending on age. We identified 37 trials for LDL‐C lowering (284 301 participants) and 11 for triglyceride lowering (120 984 participants). Overall, we found a higher risk of hemorrhagic stroke for LDL‐C lowering, risk ratio (RR) 1.16 (95% CI, 1.01–1.32, P =0.03). For statins (33 trials, 216 258 participants), RR=1.17 (95% CI, 1.01–1.36); for PCSK‐9 inhibitors (2 trials, 46 488 participants), RR=0.86 (95% CI, 0.43–1.74); and for ezetimibe (2 trials, 21 555 participants), RR=1.14 (95% CI, 0.64–2.03). In statin trials of patients with previous stroke/transient ischemic attack, RR was 1.46 (95% CI, 1.05–2.04), and in trials with mean age ≥65 years old, RR=1.34 (95% CI, 1.04–1.73) ( P int =0.14 and P int =0.23 respectively); for triglyceride lowering (11 trials, 120 984 participants), RR=1.05 (95% CI, 0.86–1.30). Conclusions We found evidence for a small increased risk of hemorrhagic stroke events with LDL‐C–lowering therapies but no clear evidence for triglyceride‐lowering therapies. Registration URL: https://www.crd.york.ac.uk/prospero ; Unique identifier: CRD42021275363.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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