Cognitive function, depressive symptoms and syphilis in HIV-positive and HIV-negative individuals

Author:

De Francesco Davide1ORCID,Winston Alan2,Underwood Jonathan2ORCID,Cresswell Fiona V34ORCID,Anderson Jane5,Post Frank A6,Williams Ian7,Mallon Patrick WG8,Sachikonye Memory9,Babalis Daphne10,Vera Jaime H311,Bagkeris Emmanouil1,Milinkovic Ana12,Sabin Caroline A1

Affiliation:

1. Institute for Global Health, UCL, London, UK

2. Division of Infectious Diseases, Imperial College London, London, UK

3. Brighton and Sussex University Hospitals NHS Trust, Brighton, UK

4. Department of Clinical Research, London School of Hygiene and Tropical Medicine, London, UK

5. Homerton University Hospital, London, UK

6. King’s College Hospital NHS Foundation Trust, London, UK

7. Mortimer Market Centre, UCL, London, UK

8. UCD School of Medicine, Dublin, Ireland

9. UK Community Advisory Board, London, UK

10. Imperial Clinical Trials Unit, Imperial College London, London, UK

11. Brighton and Sussex Medical School, University of Sussex, Brighton, UK

12. Chelsea and Westminster Healthcare NHS Foundation Trust, London, UK

Abstract

We evaluated associations between history of syphilis infection and both cognitive function and depressive symptoms in people living with HIV (PLHIV) and comparable HIV-negative controls. Syphilis serological tests, cognitive function and depression were assessed in PLHIV and controls participating in the Pharmacokinetic and Clinical Observations in People Over Fifty study. Cognitive test scores were converted to demographically adjusted T-scores (mean = 50, SD = 10) and then averaged to obtain a global T-score. Severity of depressive symptoms was assessed via the Patient Health Questionnaire-9. Associations of syphilis with global T-scores and depression were assessed using median regression. The 623 PLHIV and 246 HIV-negative controls were predominantly male (89.3% and 66.5%) with median age (interquartile range [IQR]) of 57 (53–63) and 58 (53–63) years, respectively. PLHIV had lower global cognitive T-scores (median [IQR] 48.7 [45.1, 52.1] versus 50.5 [47.0, 53.9], p < 0.001), more severe depressive symptoms (median [IQR] 4 [1, 10] versus 1 [0, 3], p < 0.001) and were more likely to report history of syphilis infection (22.0% versus 8.1%) than controls. There was no significant association between history of syphilis and global cognitive function in either PLHIV (p = 0.69) or controls (p = 0.10). Participants with a history of syphilis had more severe depressive symptoms (median [IQR] 4 [1, 9] versus 2 [0, 8], p = 0.03); however, the association became non-significant (p = 0.62) after adjusting for HIV status and potential confounders. Despite the higher prevalence of syphilis infection in PLHIV, there was no evidence of an association between history of syphilis infection and impaired cognitive function nor depressive symptoms after accounting for potential confounders.

Funder

BMS, Gilead Sciences, Janssen, Merck and ViiV Healthcare

Publisher

SAGE Publications

Subject

Infectious Diseases,Pharmacology (medical),Public Health, Environmental and Occupational Health,Dermatology

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