Skip to main content
. Author manuscript; available in PMC: 2019 Mar 1.
Published in final edited form as: Schizophr Res. 2017 Aug 19;193:161–167. doi: 10.1016/j.schres.2017.08.001

Table 1.

HSV-1 exposure and temporal trajectory of cognitive function in published studies.

First author / Reference Study sample (N) Cognitive tests Follow up duration Key results
Strandberg (Strandberg et al., 2003) Random sample of Helsinki residents with cardiovascular disease (383) MMSE, CDR 1 year Reduction in MMSE scores proportional to viral burden due to HSV-1, CMV and HSV-2
Aiello (Aiello et al., 2008) Community-dwelling elderly Latino sample (1204) MMSE, episodic memory (word list-learning test) 4 years Rate of cognitive decline significantly related to CMV titers, but not HSV-1 titers
Prasad (Prasad et al., 2012) First-episode antipsychotic-naive SZ patients (26); Healthy subjects (38) WCST 1 year Greater reduction in perseverative errors in HSV-1 seronegative SZ patients than in the HSV-1-seropositive patients. No significant associations with CMV, or in healthy subjects.
Barnes (Barnes et al., 2014) 3 cohorts of elderly community members (N=849) MMSE, tests of working memory, episodic memory, visuospatial function 5 years No significant temporal associations with HSV-1 status. CMV seropositivity associated with greater risk of Alzheimer disease and faster rate of cognitive decline in global cognition.
Nimgaonkar (Nimgaonkar et al., 2016) Representative community sample of elders MMSE, tests of complex attention, executive functions, memory, language, visuospatial function 5 years IgG titers of antibodies to CMV, HSV-2 and Tox associated with differing patterns of greater cognitive decline. No temporal associations with HSV-1.

MMSE: Mini-Mental State Examination; CDR: Clinical Dementia Rating scale; HSV-1: herpes simplex virus, type 1 (HSV-1); CMV: cytomegalovirus; HSV-2: herpes simplex virus, type 2 (HSV-2); Tox: Toxoplasma Gondii.