Colorized electron micrograph of the herpes simplex virus (HSV)

Antiviral Treatment Fails to Slow Early-Stage Alzheimer’s

The idea that herpes infections trigger or contribute to Alzheimer’s disease has been gaining favor among some scientists, raising hope that herpes treatments could slow progression of Alzheimer’s symptoms among patients.

But the first clinical trial to test that theory has found that a common antiviral for herpes simplex infections, valacyclovir, does not change the course of the disease for patients in the early stages of Alzheimer's.

Results from the trial, led by researchers at Columbia University Vagelos College of Physicians and Surgeons, were published Dec. 17 in the Journal of the American Medical Association.

Possible link between herpes viruses and Alzheimer’s disease

Approximately 60% to 70% of Americans are infected with herpes simplex viruses, which cause cold sores (usually HSV1) and genital herpes (HSV2). After signs of the initial infection subside, the viruses remain dormantwithin the nervous system and can periodically reactivate, causing symptoms to flare up.

Various studies have found connections between herpes infections and Alzheimer’s, including an autopsy study that found HSV1 DNA was often associated with amyloid plaques in the brains of people diagnosed with Alzheimer’s. Additional studies have found that people treated for herpes infections were less likely to be later diagnosed  with Alzheimer’s than HSV-positive people who received no antiviral treatment.

“Based on those previous studies, there was hope that valacyclovir could have an effect,” says the trial’s lead investigator, D.P. Devanand, professor of psychiatry and neurology and director of geriatric psychiatry.

“But no one had conducted a clinical trial to test the idea.”

Trial details

The trial included 120 adults, age 71 on average, all diagnosed with early Alzheimer’s disease or mild cognitive impairment with imaging or blood tests that indicated Alzheimer’s pathology. All participants had antibodies revealing past herpes infections (mostly HSV1, some HSV2).

The participants were randomly assigned to take daily pills containing either valacyclovir or a placebo. The researchers measured the patients’ memory functions and imaged the brain to look for amyloid and tau deposits associated with Alzheimer’s and other structural changes.

After 18 months, the researchers found that patients taking the placebo performed slightly better on cognitive tests than the valacyclovir group, but no other measures were significantly different.

“We were looking for a signal that the drug did better than the placebo, but there wasn’t any in this study,” Devanand says. “On the other measures, sometimes the placebo group did slightly better, sometimes the treatment group did slightly better.”

Grouping participants by age, sex, and apolipoprotein E e4 status did not affect the results.

“Our trial suggests antivirals that target herpes are not effective in treating early Alzheimer’s and cannot be recommended to treat such patients with evidence of prior HSV infection. We do not know if long-term antiviral medication treatment following herpes infection can prevent Alzheimer’s because prospective controlled trials have not been conducted.”

 

References

Additional information

This article originally appeared in the CUIMC Newsroom on July 29, 2025, after the results were presented the same day at the Alzheimer’s Association International Conference in Toronto, Canada.

The study, "Valacyclovir Treatment of Early Symptomatic Alzheimer Disease: The VALAD Randomized Clinical Trial," was published in JAMA on Dec. 17 with an accompanying editorial.

All authors: D. P. Devanand (Columbia), Thomas Wisniewski (New York University), Qolamreza Razlighi (Weill-Cornell Medical Center), Min Qian (Columbia), Renjie Wei (Columbia), Howard F. Andrews (Columbia), Edward P. Acosta (University of Alabama), Karen L. Bell (Columbia), Gregory H. Pelton (Columbia), Deborah Deliyannides (Columbia), Allison C. Perrin (University of Arizona), Elise Caccappolo (Columbia), Anne A. Gershon (Columbia), K. M. Prasad (University of Pittsburgh), William C. Kreisl (Columbia), Akiva Mintz (Columbia), and Edward D. Huey (Brown University).

The study was supported by grants from the National Institutes of Health (R01AG055422 and P30AG066512) and the Alzheimer's Association.

Among the Columbia authors: D. P. Devanand reported being a consultant to Acadia, Eisai, GSK, and Cybin; Karen Bell reported receiving grant support from Lilly, Amylx, and Biohaven; Anne Gershon reported having a contract with Merck; William Kreisl is now employed at Esai and was was a consultant to Cerveau and Enigma Biomedical Group while employed at Columbia; and Akiva Mintz reported receiving personal fees from Siemens and ICON and receiving grants from Alexion and Regeneron. See the paper for other disclosures.