PMID- 23080504 OWN - NLM STAT- MEDLINE DCOM- 20130326 LR - 20181202 IS - 1096-9071 (Electronic) IS - 0146-6615 (Linking) VI - 84 IP - 12 DP - 2012 Dec TI - Response to valganciclovir in chronic fatigue syndrome patients with human herpesvirus 6 and Epstein-Barr virus IgG antibody titers. PG - 1967-74 LID - 10.1002/jmv.23411 [doi] AB - Valganciclovir has been reported to improve physical and cognitive symptoms in patients with chronic fatigue syndrome (CFS) with elevated human herpesvirus 6 (HHV-6) and Epstein-Barr virus (EBV) IgG antibody titers. This study investigated whether antibody titers against HHV-6 and EBV were associated with clinical response to valganciclovir in a subset of CFS patients. An uncontrolled, unblinded retrospective chart review was performed on 61 CFS patients treated with 900 mg valganciclovir daily (55 of whom took an induction dose of 1,800 mg daily for the first 3 weeks). Antibody titers were considered high if HHV-6 IgG >/= 1:320, EBV viral capsid antigen (VCA) IgG >/= 1:640, and EBV early antigen (EA) IgG >/= 1:160. Patients self-rated physical and cognitive functioning as a percentage of their functioning prior to illness. Patients were categorized as responders if they experienced at least 30% improvement in physical and/or cognitive functioning. Thirty-two patients (52%) were categorized as responders. Among these, 19 patients (59%) responded physically and 26 patients (81%) responded cognitively. Baseline antibody titers showed no significant association with response. After treatment, the average change in physical and cognitive functioning levels for all patients was +19% and +23%, respectively (P < 0.0001). Longer treatment was associated with improved response (P = 0.0002). No significant difference was found between responders and non-responders among other variables analyzed. Valganciclovir treatment, independent of the baseline antibody titers, was associated with self-rated improvement in physical and cognitive functioning for CFS patients who had positive HHV-6 and/or EBV serologies. Longer valganciclovir treatment correlated with an improved response. CI - Copyright (c) 2012 Wiley Periodicals, Inc. FAU - Watt, Tessa AU - Watt T AD - Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University Medical Center, Palo Alto, CA, USA. FAU - Oberfoell, Stephanie AU - Oberfoell S FAU - Balise, Raymond AU - Balise R FAU - Lunn, Mitchell R AU - Lunn MR FAU - Kar, Aroop K AU - Kar AK FAU - Merrihew, Lindsey AU - Merrihew L FAU - Bhangoo, Munveer S AU - Bhangoo MS FAU - Montoya, Jose G AU - Montoya JG LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - J Med Virol JT - Journal of medical virology JID - 7705876 RN - 0 (Antibodies, Viral) RN - 0 (Antigens, Viral) RN - 0 (Antiviral Agents) RN - 0 (Capsid Proteins) RN - 0 (Epstein-Barr viral capsid antigen) RN - 0 (Epstein-Barr virus early antigen) RN - GCU97FKN3R (Valganciclovir) RN - P9G3CKZ4P5 (Ganciclovir) SB - IM MH - Adult MH - Antibodies, Viral/*blood/immunology MH - Antigens, Viral/analysis/immunology MH - Antiviral Agents/administration & dosage/*therapeutic use MH - Capsid Proteins/analysis/immunology MH - Cognition/drug effects MH - Drug Administration Schedule MH - Drug Evaluation MH - Fatigue Syndrome, Chronic/*drug therapy/immunology/virology MH - Female MH - Ganciclovir/administration & dosage/*analogs & derivatives/therapeutic use MH - Herpesvirus 4, Human/*immunology MH - Herpesvirus 6, Human/*immunology MH - Humans MH - Male MH - Middle Aged MH - Retrospective Studies MH - Self Report MH - Treatment Outcome MH - Valganciclovir EDAT- 2012/10/20 06:00 MHDA- 2013/03/27 06:00 CRDT- 2012/10/20 06:00 PHST- 2012/10/20 06:00 [entrez] PHST- 2012/10/20 06:00 [pubmed] PHST- 2013/03/27 06:00 [medline] AID - 10.1002/jmv.23411 [doi] PST - ppublish SO - J Med Virol. 2012 Dec;84(12):1967-74. doi: 10.1002/jmv.23411.