Cholesterol lowering drugs not linked to dementia

Publicly released:
Australia; VIC; WA; TAS

The use of statins to lower cholesterol in adults over 65 years is not linked with the development of dementia, or mild cognitive impairment, according to Australian research. In 2012 the US Food and Drug Administration released a warning about cases of apparent short-term cognitive impairment with statin use, but research on this link has shown mixed results. The researchers used data from the Australian ASPREE trial which was designed to look at the use of Aspirin in the elderly, as participants had a cognitive screening test when they were enrolled in the study. Looking at those taking statins at the start of the study compared to those who were not, they found no difference in the risk of dementia, probable Alzheimer's or cognitive decline over the 4.7 years of the study.  

Media release

From: American College of Cardiology

Statin Therapy Not Associated With Cognitive Decline, Dementia in Older Adults, Study Says
Observational study adds to growing evidence on statins, but randomized trials are still needed

WASHINGTON (June 21, 2021) — The use of statin therapy in adults 65 years old or older is not associated with incident dementia, mild cognitive impairment (MCI) or decline in individual cognition domains, according to a study published in the Journal of the American College of Cardiology (JACC).

Cognitive decline and dementia are major health concerns in older individuals, affecting about 10% of people over 60 years old. Statins are used to reduce low-density lipoprotein cholesterol, or bad cholesterol, thus they are a fundamental treatment for prevention of primary and secondary cardiovascular disease (CVD) events. The Food and Drug Administration released a warning in 2012 about cases of apparent short-term cognitive impairment with statin use, while acknowledging that the cardiovascular benefits outweigh their risks. However, systematic reviews have shown insufficient evidence on the impact of statins and research has shown mixed results, with some showing a neurocognitive benefit of statins and others reporting a null effect. According to the researchers of this study, since statins are widely used among older adults and expected to increase in use, determining the effects of statin therapy on cognition in older individuals is vital to help clinicians weigh their benefits against associated risks.

“With statins being increasingly prescribed to older adults, their potential long-term effects on cognitive decline and dementia risk have attracted growing interest,” said Zhen Zhou, PhD, Menzies Institute for Medical Research at the University of Tasmania in Australia and lead author of the study. “The present study adds to previous research by suggesting that statin use at baseline was not associated with subsequent dementia incidence and long-term cognitive decline in older adults.”

Researchers of this study analyzed data from the ASPirin in Reducing Events in the Elderly (ASPREE) trial. ASPREE was a large prospective, randomized placebo-controlled trial of daily low-dose aspirin, which included 19,114 participants 65 years old or older with no prior CVD event, dementia or major physical disability, between 2010 and 2014 from Australia and the U.S. One of the key selection criteria of ASPREE was that participants had to have a score of ≥78 for the Modified Mini-Mental State Examination test, a screening test for cognitive abilities, at enrollment.

Researchers excluded participants with missing values for cognitive test scores and/or covariates at baseline, resulting in 18,846 participants. They were grouped by their baseline statin use versus non-statin use, with 5,898 (31.3%) of participants taking statins. The study aimed to measure outcomes including incident dementia and its subclassifications (probable Alzheimer’s disease [AD], mixed presentations); MCI and its subclassifications (MCI consistent with AD, MCI-other); changes in domain-specific cognition including global cognition, memory, language and executive function, and psychomotor speed; and in the composite of these domains.

After a median of 4.7 years of follow-up, researchers found 566 incident cases of dementia (including probable AD and mixed presentations). Compared with no statin use, statin use was not associated with risk of all-cause dementia, probable AD or mixed presentations of dementia. There were 380 incident cases of MCI found (including MCI consistent with AD and MCI-other). Compared to no statin use, statin use was not associated with risk of MCI, MCI consistent with AD or other MCI. There was no statistically significant difference in the change of composite cognition and any individual cognitive domains between statin users versus non-statin users. Also, no significant differences were found in any of the outcomes of interest between users of hydrophilic and lipophilic statins. However, researchers did find interaction effects between baseline cognitive ability and statin therapy for all dementia outcomes.

According to the researchers, this study has several limitations, including observational study bias, lack of data on the length of prior use of statins and the dose of statins was not recorded in the ASPREE trial, so their effects could not be fully explored. Researchers conclude the study must be interpreted with caution and will require confirmation by randomized clinical trials designed to explore the neurocognitive effects of statins in older populations.

In an accompanying editorial comment, Christie M. Ballantyne, MD, professor at Baylor College of Medicine in Houston, said the study does have limitations that the authors address, but agreed the findings suggest statins do not contribute to cognitive decline.

“Overall, the analysis was well done, and its main strengths are a large cohort with a battery of standardized tests that allowed the investigators to track both cognition and incidence of dementia and its subtypes over time,” Ballantyne said. “Lingering questions such as the one raised by this analysis regarding potential adverse effects of statins in individuals with mildly impaired cognition can only be answered in randomized controlled trials in the appropriate age group and population and with appropriate testing and adequate follow-up. In the meantime, practicing clinicians can have confidence and share with their patients that short-term lipid lowering therapy in older individuals, including with statins, is unlikely to have a major impact on cognition.”

The American College of Cardiology envisions a world where innovation and knowledge optimize cardiovascular care and outcomes. As the professional home for the entire cardiovascular care team, the mission of the College and its 54,000 members is to transform cardiovascular care and to improve heart health. The ACC bestows credentials upon cardiovascular professionals who meet stringent qualifications and leads in the formation of health policy, standards and guidelines. The College also provides professional medical education, disseminates cardiovascular research through its world-renowned JACC Journals, operates national registries to measure and improve care, and offers cardiovascular accreditation to hospitals and institutions. For more, visit acc.org.

The Journal of the American College of Cardiology ranks among the top cardiovascular journals in the world for its scientific impact. JACC is the flagship for a family of journals—JACC: Cardiovascular Interventions, JACC: Cardiovascular Imaging, JACC: Heart Failure, JACC: Clinical Electrophysiology, JACC: Basic to Translational Science, JACC: Case Reports, JACC: CardioOncology and JACC: Asia—that prides themselves in publishing the top peer-reviewed research on all aspects of cardiovascular disease. Learn more at JACC.org.

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Organisation/s: Menzies Institute for Medical Research, Monash University, Curtin University
Funder: The ASPREE trial was supported by a grant (U01AG029824) from the National Institute on Aging and the National Cancer Institute at the National Institutes of Health, by grants (334047 and 1127060) from the National Health and Medical Research Council of Australia, and by Monash University and the Victorian Cancer Agency. Dr. Tonkin has received research support or honoraria from Merck, Pfizer, and Amgen; has received support from Bayer for materials in the ASPREE trial; and has received National Health and Medical Research Council (NHMRC) grant support for the STAREE trial. Dr. Zoungas has received NHMRC and Australian Heart Foundation research funding as the principal investigator of the STAREE trial; and has received payment to the institution (Monash University) from Eli Lilly Australia, Boehringer-Ingelheim, Merck Sharp & Dohme Australia, AstraZeneca, Novo Nordisk, Sanofi, and Servier for consultancy work outside the submitted work. Dr. Nelson has received honoraria from Sanofi and Amgen; has received support from Bayer for materials in ASPREE; and has received NHMRC grant support for STAREE. Dr. Reid is funded through a NHMRC Principal Research Fellowship. Dr. Shah serves as a noncompensated member of the board of directors of the Alzheimer’s Association, Illinois Chapter; receives research support to his institution, Rush University Medical Center, for his role as a site principal investigator or site subinvestigator for industry-initiated clinical trials and research studies of AD sponsored by Amylyx Pharmaceuticals, Eli Lilly, Genentech, Lundbeck, Merck, Navidea Biopharmaceuticals, Novartis Pharmaceuticals, Roche Holdings, and Takeda Development Center Americas; and is a member of the steering committee of the PREVENTABLE clinical trial.
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