# The effects of cholesterol-lowering drugs on neurocognitive function: systematic review and meta analysis

**Authors:** Kaiwei Li, Ying Li, Xia Jiang, Ye Zhu

PMC · DOI: 10.3389/fneur.2026.1696228 · Frontiers in Neurology · 2026-02-04

## TL;DR

This study finds that cholesterol-lowering drugs do not harm neurocognitive function or increase the risk of cognitive issues.

## Contribution

The study provides a comprehensive meta-analysis showing no adverse neurocognitive effects from cholesterol-lowering drugs.

## Key findings

- Cholesterol-lowering drugs do not increase the risk of neurocognitive events.
- No significant impact on cognitive domains like attention, memory, and executive function was observed.
- Statins, ezetimibe, and PCSK9 inhibitors all showed similar safety profiles regarding cognitive function.

## Abstract

To investigate if cholesterol-lowering drugs exert effects on neurocognitive function.

We searched Pubmed, Embase and Cochrane Libarary from inception to March 23rd, 2023, and searched clinicaltrials.gov on January 23rd, 2024. Randomized controlled trials that evaluated neurocognitive events and neurocognitive function after using cholesterol-lowering drugs including statins, cholesterol absorption inhibitors, proprotein convertase subtilisin/kexin 9 inhibitors were collected. The literature screening, data extraction and quality evaluation were carried out independently by two researchers, and the random effect model was used to pool the data.

A total of 42 studies with 150,405 subjects were included. Cholesterol-lowering drugs did not increase the risk of neurocognitive events (RR: 0.99, 95% CI: 0.88–1.12). Subgroup analysis by the type of drugs did not suggest that statins (RR: 0.94, 95% CI: 0.72–1.25), ezetimibe (RR: 1.11, 95% CI: 0.71–1.74) or proprotein convertase subtilisin/kexin 9 inhibitors (RR: 1.00, 95% CI: 0.87–1.14) increased the risk of neurocognitive events. By pooling the outcomes of the neurocognitive test scale, we found that cholesterol-lowering drugs did not change neurocognitive function in the five domains of attention, psychomotor speed, executive function, working memory and memory, as well as global effect.

Cholesterol-lowering drugs including statins, cholesterol absorption inhibitors and PCSK9 inhibitors have no adverse effects on neurocognitive function. The decrease of low-density lipoprotein cholesterol will not lead to the decline of neurocognitive function.

https://www.crd.york.ac.uk/PROSPERO/view/CRD42023404802, Identifier: CRD42023404802

## Linked entities

- **Chemicals:** ezetimibe (PubChem CID 150311)

## Full-text entities

- **Genes:** PCSK9 (proprotein convertase subtilisin/kexin type 9) [NCBI Gene 255738] {aka FH3, FHCL3, HCHOLA3, LDLCQ1, NARC-1, NARC1}, NPC1L1 (NPC1 like intracellular cholesterol transporter 1) [NCBI Gene 29881] {aka LDLCQ7, NPC11L1, SLC65A2}
- **Diseases:** aphasia (MESH:D001037), ACS (MESH:D000168), adverse drug reaction (MESH:D064420), familial hypercholesterolemia (MESH:D006938), attention disorders (MESH:D001289), acute myocardial infarction (MESH:D009203), impaired neurocognitive function (MESH:D019965), ASCVD (MESH:D050197), vascular dementia (MESH:D015140), vascular encephalopathy (MESH:D001927), hallucinations (MESH:D006212), FH (OMIM:143890), memory impairment (MESH:D008569), cognitive decline (MESH:D003072), amnesia (MESH:D000647), frontotemporal dementia (MESH:D057180), coronary artery disease (MESH:D003324), type 1 diabetes mellitus (MESH:D003922), dementia (MESH:D003704), hypercholesterolemia (MESH:D006937), type 2 diabetes mellitus (MESH:D003924), schizophrenia (MESH:D012559), Alzheimer's disease (MESH:D000544), decline of neurocognitive function (MESH:D060825), acute coronary syndrome (MESH:D054058), coronary heart disease (MESH:D003327), neurocognitive diseases (MESH:D004194), reading disorders (MESH:D004410), SLE (MESH:D008180), stroke (MESH:D020521), confusion (MESH:D003221), COPD (MESH:D029424), delirium (MESH:D003693)
- **Chemicals:** pravastatin (MESH:D017035), atorvastatin (MESH:D000069059), cholesterol absorption (-), Simvastatin (MESH:D019821), lipid (MESH:D008055), bococizumab (MESH:C000598888), Alirocumab (MESH:C571059), Ezetimibe (MESH:D000069438), Evolocumab (MESH:C577155), Cholesterol (MESH:D002784), lovastatin (MESH:D008148), phospholipids (MESH:D010743)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12913106/full.md

## Figures

19 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12913106/full.md

## References

73 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913106/full.md

---
Source: https://tomesphere.com/paper/PMC12913106