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Cholesterol-fighting drugs lower risk of Alzheimers disease
The incidence of Alzheimers was reduced for beneficiaries frequently prescribed statins (high users), compared to low users, researchers find
Common anti-cholesterol drugs show promise for reducing the risk of Alzheimers disease, a USC-led study of Medicare data reveals.
The new study shows that, based on a sample of 399,979 Medicare beneficiaries, men and women who took statins two years or more lowered their risk of Alzheimers in the period spanning 2009 to 2013.
The incidence of Alzheimers disease was reduced for beneficiaries frequently prescribed statins (high users), compared to low users, USC and University of Arizona researchers found. Among women who were high users, the incidence rate was 15 percent lower. Among men, the rate was 12 percent lower.
Researchers noted that black men were the only group that did not show a statistically significant reduction in risk, likely due to sample size.
We may not need to wait for a cure to make a difference for patients currently at risk of the disease. Existing drugs, alone or in combination, may affect Alzheimers risk, said lead and corresponding author Julie Zissimopoulos, associate director of the USC Leonard D. Schaeffer Center for Health Policy and Economics and assistant professor at USC Price School of Public Policy.
Prior studies have shown a link between cholesterol and the hallmark of Alzheimers disease: the beta-amyloid plaques that interfere with memory and other brain functions.
We looked to statins as a candidate because they are widely used and have resulted in the reduction of cholesterol, she said.
The findings were published on Dec. 12 in JAMA Neurology.
Urgent need for treatment
Although much is known about Alzheimers, scientists have been unsuccessful so far in developing effective treatments to prevent and slow the memory-erasing disease that affects more than 5 million Americans. Hopes were high for the Eli Lilly-designed experimental drug solanezumab that aimed to attack the amyloid plaques. The drug failed for patients with mild dementia in a recent large clinical trial.
Beta-amyloid continues to be a therapeutic target; however, once a patient is symptomatic and has the plaques, it may be too late, Zissimopoulos said. Some researchers believe successful treatment may involve a cocktail of several medications aimed at multiple targets.
Age-related diseases are among the intractable problems that USC researchers in multiple disciplines are seeking to unravel. Efforts to understand Alzheimers and dementia and to find preventive interventions and precise treatments are much more pressing as the baby boomer generation ages.
In a previous study, Zissimopoulos found that if medical advances could delay the diseases onset by a year, more than 2 million Americans would be spared from developing Alzheimers. This also would result in a $220 billion savings in health and caregiving costs by 2050.
Zissimopoulos cautioned that a silver tsunami of aging baby boomers will increase the number of Alzheimers patients 70 and older to 9.1 million by 2050. Annual health care costs will surge to $1.5 trillion.
High users vs. low users
Other studies have compared statin users to non-statin users with a range of health statuses. However, Zissimopoulos said the USC-led team focused only on statin users.
The research team divided the patients into two groups: high-use beneficiaries those who took statins for two years or more between 2006 and 2008 and low-use beneficiaries who took them less frequently or who started taking statins after 2008. Both sets of beneficiaries were in similar health and had no diagnosis of Alzheimers disease. The researchers studied records dating from 2009 to 2013 to track the onset of Alzheimers.
The estimated 400,000 Medicare beneficiaries who became the focus of the study were 65 and older as of January 2006 and were continuously enrolled in Medicare fee-for-service and Part D prescription drug coverage. The study sought results on four of the most commonly prescribed statins: simvastatin, atorvastatin, pravastatin and rosuvastatin.
The researchers also found a reduction in risk for certain demographic groups who were frequently prescribed statins for two years or more.
The greatest drop in incidence of Alzheimers disease 29 percent was among Hispanic men. Among white men, high users of statins had an 11-percent lower risk of incidence of the disease. A similar reduction in risk 12-percent was found among Hispanic women.
The risk of Alzheimers disease was also lower for white women who were high users (15 percent lower than women who took statins less frequently).
Reduced risks
Simvastatin was linked to a reduced risk of Alzheimers for white women, Hispanic women and black women, as well as for white men and Hispanic men. Atrovastatin was associated with a reduced risk of Alzheimers for white women, Hispanic women, black women and Hispanic men.
Pravastatin and rosuvastatin results showed a statistically significant reduction of Alzheimers risk for only white women.
Some scientists believe that certain statins such as atorvastatin and simvastatin, known as lipophilics, would be most effective as an Alzheimers preventive treatment because they cross the blood-brain barrier, a protective layer of cells that restricts the types of substances that can pass to the brain.
We generally found that theyre all associated with reduced risk, Zissimopoulos said.
The researchers plan to study combinations of other existing drugs to measure their effects on the risk of Alzheimers.
Anti-diabetic drugs have been linked to lower incidence of Alzheimers disease, as have some anti-hypertensives, said study co-author Geoffrey Joyce, director of health policy for the USC Schaeffer Center and an associate professor at the USC School of Pharmacy. But there is mixed evidence across the cardiovascular drug classes.
The study was supported with a grant from the National Institute on Aging of the National Institutes of Health and the USC Zumberge Research Fund.
Study co-authors were Douglas Barthold of the USC Schaeffer Center and Roberta Diaz Brinton, formerly of the USC School of Pharmacy and now with the University of Arizona.