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Antiviral therapy: Valacyclovir Treatment of Alzheimer’s Disease (VALAD) Trial: protocol for a randomised, double-blind,placebo-controlled, treatment trial

IntroductionAfter infection, herpes simplex virus-1 (HSV1) becomes latent in the trigeminal ganglion and can enter the brain via retrograde axonal transport. Recurrent reactivation of HSV1 may lead to neurodegeneration and Alzheimer’s disease (AD) pathology. HSV1 (oral herpes) and HSV2 (genital herp...

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Published in:BMJ open 2020-02, Vol.10 (2), p.e032112
Main Authors: Devanand, D P, Andrews, Howard, Kreisl, William C, Razlighi, Qolamreza, Gershon, Anne, Stern, Yaakov, Mintz, Akiva, Wisniewski, Thomas, Acosta, Edward, Pollina, Julianna, Katsikoumbas, Mariasofia, Bell, Karen L, Pelton, Gregory H, Deliyannides, Deborah, Prasad, K M, Huey, Edward D
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container_issue 2
container_start_page e032112
container_title BMJ open
container_volume 10
creator Devanand, D P
Andrews, Howard
Kreisl, William C
Razlighi, Qolamreza
Gershon, Anne
Stern, Yaakov
Mintz, Akiva
Wisniewski, Thomas
Acosta, Edward
Pollina, Julianna
Katsikoumbas, Mariasofia
Bell, Karen L
Pelton, Gregory H
Deliyannides, Deborah
Prasad, K M
Huey, Edward D
description IntroductionAfter infection, herpes simplex virus-1 (HSV1) becomes latent in the trigeminal ganglion and can enter the brain via retrograde axonal transport. Recurrent reactivation of HSV1 may lead to neurodegeneration and Alzheimer’s disease (AD) pathology. HSV1 (oral herpes) and HSV2 (genital herpes) can trigger amyloid beta-protein (Aβ) aggregation and HSV1 DNA is common in amyloid plaques. Anti-HSV drugs reduce Aβ and phosphorylated tau accumulation in cell-culture models. Cognitive impairment is greater in patients with HSV seropositive, and antiviral drugs show robust efficacy against peripheral HSV infection. Recent studies of electronic health records databases demonstrate that HSV infections increase dementia risk, and that antiviral medication treatment reduces this risk. The generic antiviral drug valacyclovir was superior to placebo in improving memory in a schizophrenia pilot trial but has not been tested in AD.Methods and analysisIn patients with mild AD who test positive for HSV1 or HSV2 serum antibodies, valacyclovir, repurposed as an anti-AD drug, will be compared with placebo (lactose pills) in 130 patients (65 valacyclovir and 65 placebo) in a randomised, double-blind, 78-week phase II proof-of-concept trial. Patients on valacyclovir, dose-titrated from 2 g to a targeted oral dose of 4 g daily, compared with placebo, are hypothesised to show smaller cognitive and functional decline, and, using 18F-Florbetapir positron emission tomography (PET) and 18F-MK-6240 PET imaging, to show less amyloid and tau accumulation, respectively. In the lumbar puncture subsample, cerebrospinal fluid acyclovir will be assayed to assess central nervous system valacyclovir penetration.Ethics and disseminationThe trial is being overseen by the New York State Psychiatric Institute Institutional Review Board (protocol 7537), the National Institute on Ageing, and the Data Safety Monitoring Board. Written informed consent is obtained for all subjects. Results will be disseminated via publication, clinicaltrials.gov, media and conferences.Trial registration numberClinicalTrials.gov identifier (NCT03282916) Pre-results.
doi_str_mv 10.1136/bmjopen-2019-032112
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Recurrent reactivation of HSV1 may lead to neurodegeneration and Alzheimer’s disease (AD) pathology. HSV1 (oral herpes) and HSV2 (genital herpes) can trigger amyloid beta-protein (Aβ) aggregation and HSV1 DNA is common in amyloid plaques. Anti-HSV drugs reduce Aβ and phosphorylated tau accumulation in cell-culture models. Cognitive impairment is greater in patients with HSV seropositive, and antiviral drugs show robust efficacy against peripheral HSV infection. Recent studies of electronic health records databases demonstrate that HSV infections increase dementia risk, and that antiviral medication treatment reduces this risk. The generic antiviral drug valacyclovir was superior to placebo in improving memory in a schizophrenia pilot trial but has not been tested in AD.Methods and analysisIn patients with mild AD who test positive for HSV1 or HSV2 serum antibodies, valacyclovir, repurposed as an anti-AD drug, will be compared with placebo (lactose pills) in 130 patients (65 valacyclovir and 65 placebo) in a randomised, double-blind, 78-week phase II proof-of-concept trial. Patients on valacyclovir, dose-titrated from 2 g to a targeted oral dose of 4 g daily, compared with placebo, are hypothesised to show smaller cognitive and functional decline, and, using 18F-Florbetapir positron emission tomography (PET) and 18F-MK-6240 PET imaging, to show less amyloid and tau accumulation, respectively. In the lumbar puncture subsample, cerebrospinal fluid acyclovir will be assayed to assess central nervous system valacyclovir penetration.Ethics and disseminationThe trial is being overseen by the New York State Psychiatric Institute Institutional Review Board (protocol 7537), the National Institute on Ageing, and the Data Safety Monitoring Board. Written informed consent is obtained for all subjects. Results will be disseminated via publication, clinicaltrials.gov, media and conferences.Trial registration numberClinicalTrials.gov identifier (NCT03282916) Pre-results.</description><identifier>ISSN: 2044-6055</identifier><identifier>EISSN: 2044-6055</identifier><identifier>DOI: 10.1136/bmjopen-2019-032112</identifier><identifier>PMID: 32034019</identifier><language>eng</language><publisher>England: BMJ Publishing Group LTD</publisher><subject>Alzheimer Disease - drug therapy ; Alzheimer Disease - virology ; Alzheimer's disease ; Amyloid beta-Peptides - metabolism ; Antiviral Agents - therapeutic use ; Antiviral drugs ; Brain ; Cardiovascular disease ; Cognition &amp; reasoning ; Cognitive ability ; Cognitive Dysfunction - virology ; Dementia ; Deoxyribonucleic acid ; DNA ; DNA polymerase ; Double-Blind Method ; Double-blind studies ; Drug dosages ; Female ; Herpes Simplex - complications ; Herpes Simplex - drug therapy ; Herpes viruses ; Herpesvirus 1, Human - drug effects ; Humans ; Infections ; Male ; Memory ; Middle Aged ; Neurology ; Older people ; Proteins ; Psychosis ; Randomized Controlled Trials as Topic ; Schizophrenia ; tau Proteins - metabolism ; Valacyclovir - therapeutic use ; Virus Replication - drug effects</subject><ispartof>BMJ open, 2020-02, Vol.10 (2), p.e032112</ispartof><rights>Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2020 Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. 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Recurrent reactivation of HSV1 may lead to neurodegeneration and Alzheimer’s disease (AD) pathology. HSV1 (oral herpes) and HSV2 (genital herpes) can trigger amyloid beta-protein (Aβ) aggregation and HSV1 DNA is common in amyloid plaques. Anti-HSV drugs reduce Aβ and phosphorylated tau accumulation in cell-culture models. Cognitive impairment is greater in patients with HSV seropositive, and antiviral drugs show robust efficacy against peripheral HSV infection. Recent studies of electronic health records databases demonstrate that HSV infections increase dementia risk, and that antiviral medication treatment reduces this risk. The generic antiviral drug valacyclovir was superior to placebo in improving memory in a schizophrenia pilot trial but has not been tested in AD.Methods and analysisIn patients with mild AD who test positive for HSV1 or HSV2 serum antibodies, valacyclovir, repurposed as an anti-AD drug, will be compared with placebo (lactose pills) in 130 patients (65 valacyclovir and 65 placebo) in a randomised, double-blind, 78-week phase II proof-of-concept trial. Patients on valacyclovir, dose-titrated from 2 g to a targeted oral dose of 4 g daily, compared with placebo, are hypothesised to show smaller cognitive and functional decline, and, using 18F-Florbetapir positron emission tomography (PET) and 18F-MK-6240 PET imaging, to show less amyloid and tau accumulation, respectively. In the lumbar puncture subsample, cerebrospinal fluid acyclovir will be assayed to assess central nervous system valacyclovir penetration.Ethics and disseminationThe trial is being overseen by the New York State Psychiatric Institute Institutional Review Board (protocol 7537), the National Institute on Ageing, and the Data Safety Monitoring Board. Written informed consent is obtained for all subjects. 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Andrews, Howard ; Kreisl, William C ; Razlighi, Qolamreza ; Gershon, Anne ; Stern, Yaakov ; Mintz, Akiva ; Wisniewski, Thomas ; Acosta, Edward ; Pollina, Julianna ; Katsikoumbas, Mariasofia ; Bell, Karen L ; Pelton, Gregory H ; Deliyannides, Deborah ; Prasad, K M ; Huey, Edward D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b538t-3c551dc218d725d89d4d84212e4fa5c149d2fcbd334c863a49d46c62424d57123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Alzheimer Disease - drug therapy</topic><topic>Alzheimer Disease - virology</topic><topic>Alzheimer's disease</topic><topic>Amyloid beta-Peptides - metabolism</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Antiviral drugs</topic><topic>Brain</topic><topic>Cardiovascular disease</topic><topic>Cognition &amp; reasoning</topic><topic>Cognitive ability</topic><topic>Cognitive Dysfunction - virology</topic><topic>Dementia</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA polymerase</topic><topic>Double-Blind Method</topic><topic>Double-blind studies</topic><topic>Drug dosages</topic><topic>Female</topic><topic>Herpes Simplex - complications</topic><topic>Herpes Simplex - drug therapy</topic><topic>Herpes viruses</topic><topic>Herpesvirus 1, Human - drug effects</topic><topic>Humans</topic><topic>Infections</topic><topic>Male</topic><topic>Memory</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Older people</topic><topic>Proteins</topic><topic>Psychosis</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Schizophrenia</topic><topic>tau Proteins - metabolism</topic><topic>Valacyclovir - therapeutic use</topic><topic>Virus Replication - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Devanand, D P</creatorcontrib><creatorcontrib>Andrews, Howard</creatorcontrib><creatorcontrib>Kreisl, William C</creatorcontrib><creatorcontrib>Razlighi, Qolamreza</creatorcontrib><creatorcontrib>Gershon, Anne</creatorcontrib><creatorcontrib>Stern, Yaakov</creatorcontrib><creatorcontrib>Mintz, Akiva</creatorcontrib><creatorcontrib>Wisniewski, Thomas</creatorcontrib><creatorcontrib>Acosta, Edward</creatorcontrib><creatorcontrib>Pollina, Julianna</creatorcontrib><creatorcontrib>Katsikoumbas, Mariasofia</creatorcontrib><creatorcontrib>Bell, Karen L</creatorcontrib><creatorcontrib>Pelton, Gregory H</creatorcontrib><creatorcontrib>Deliyannides, Deborah</creatorcontrib><creatorcontrib>Prasad, K M</creatorcontrib><creatorcontrib>Huey, Edward D</creatorcontrib><collection>BMJ Open Access Journals</collection><collection>BMJ Journals:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; 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Recurrent reactivation of HSV1 may lead to neurodegeneration and Alzheimer’s disease (AD) pathology. HSV1 (oral herpes) and HSV2 (genital herpes) can trigger amyloid beta-protein (Aβ) aggregation and HSV1 DNA is common in amyloid plaques. Anti-HSV drugs reduce Aβ and phosphorylated tau accumulation in cell-culture models. Cognitive impairment is greater in patients with HSV seropositive, and antiviral drugs show robust efficacy against peripheral HSV infection. Recent studies of electronic health records databases demonstrate that HSV infections increase dementia risk, and that antiviral medication treatment reduces this risk. The generic antiviral drug valacyclovir was superior to placebo in improving memory in a schizophrenia pilot trial but has not been tested in AD.Methods and analysisIn patients with mild AD who test positive for HSV1 or HSV2 serum antibodies, valacyclovir, repurposed as an anti-AD drug, will be compared with placebo (lactose pills) in 130 patients (65 valacyclovir and 65 placebo) in a randomised, double-blind, 78-week phase II proof-of-concept trial. Patients on valacyclovir, dose-titrated from 2 g to a targeted oral dose of 4 g daily, compared with placebo, are hypothesised to show smaller cognitive and functional decline, and, using 18F-Florbetapir positron emission tomography (PET) and 18F-MK-6240 PET imaging, to show less amyloid and tau accumulation, respectively. In the lumbar puncture subsample, cerebrospinal fluid acyclovir will be assayed to assess central nervous system valacyclovir penetration.Ethics and disseminationThe trial is being overseen by the New York State Psychiatric Institute Institutional Review Board (protocol 7537), the National Institute on Ageing, and the Data Safety Monitoring Board. Written informed consent is obtained for all subjects. Results will be disseminated via publication, clinicaltrials.gov, media and conferences.Trial registration numberClinicalTrials.gov identifier (NCT03282916) Pre-results.</abstract><cop>England</cop><pub>BMJ Publishing Group LTD</pub><pmid>32034019</pmid><doi>10.1136/bmjopen-2019-032112</doi><oa>free_for_read</oa></addata></record>
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ispartof BMJ open, 2020-02, Vol.10 (2), p.e032112
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2044-6055
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recordid cdi_doaj_primary_oai_doaj_org_article_203cfb36c06d4121a7b06baf3c06ea77
source BMJ Open Access Journals; Open Access: PubMed Central; Publicly Available Content (ProQuest); BMJ Journals
subjects Alzheimer Disease - drug therapy
Alzheimer Disease - virology
Alzheimer's disease
Amyloid beta-Peptides - metabolism
Antiviral Agents - therapeutic use
Antiviral drugs
Brain
Cardiovascular disease
Cognition & reasoning
Cognitive ability
Cognitive Dysfunction - virology
Dementia
Deoxyribonucleic acid
DNA
DNA polymerase
Double-Blind Method
Double-blind studies
Drug dosages
Female
Herpes Simplex - complications
Herpes Simplex - drug therapy
Herpes viruses
Herpesvirus 1, Human - drug effects
Humans
Infections
Male
Memory
Middle Aged
Neurology
Older people
Proteins
Psychosis
Randomized Controlled Trials as Topic
Schizophrenia
tau Proteins - metabolism
Valacyclovir - therapeutic use
Virus Replication - drug effects
title Antiviral therapy: Valacyclovir Treatment of Alzheimer’s Disease (VALAD) Trial: protocol for a randomised, double-blind,placebo-controlled, treatment trial
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