Cerebrospinal Fluid Viral Load Across the Spectrum of Untreated Human Immunodeficiency Virus Type 1 (HIV-1) Infection: A Cross-Sectional Multicenter Study

Author:

Ulfhammer Gustaf12ORCID,Edén Arvid12,Antinori Andrea3,Brew Bruce J4,Calcagno Andrea5ORCID,Cinque Paola6,De Zan Valentina6,Hagberg Lars12,Lin Amy7,Nilsson Staffan8,Oprea Cristiana9,Pinnetti Carmela3,Spudich Serena10,Trunfio Mattia5,Winston Alan11,Price Richard W12,Gisslén Magnus12

Affiliation:

1. Department of Infectious Diseases, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden

2. Region Västra Götaland, Sahlgrenska University Hospital, Department of Infectious Diseases, Gothenburg, Sweden

3. National Institute of Infectious Diseases L. Spallanzani, Rome, Italy

4. Departments of Neurology and Immunology, Peter Duncan Neurosciences Unit St Vincent’s Centre for Applied Medical Research, St Vincent’s Hospital, University of New South Wales and University of Notre Dame, Australia

5. Unit of Infectious Diseases, Department of Medical Sciences, University of Torino, Torino, Italy

6. Scientific Institute San Raffaele, Milan, Italy

7. Stanford University School of Medicine, Department of Biomedical Data Science, Palo Alto, California, USA

8. Mathematical Sciences, Chalmers University of Technology, Gothenburg, Sweden

9. Carol Davila University of Medicine and Pharmacy, Victor Babes Clinical Hospital for Infectious and Tropical Diseases, Bucharest, Romania

10. Yale University, New Haven, Connecticut, USA

11. Imperial College, London, United Kingdomand

12. University of California at San Francisco, San Francisco, California, USA

Abstract

Abstract Background The aim of this large multicenter study was to determine variations in cerebrospinal fluid (CSF) HIV-RNA in different phases of untreated human immunodeficiency virus type 1 (HIV-1) infection and its associations with plasma HIV-RNA and other biomarkers. Methods Treatment naive adults with available CSF HIV-RNA quantification were included and divided into groups representing significant disease phases. Plasma HIV-RNA, CSF white blood cell count (WBC), neopterin, and albumin ratio were included when available. Results In total, 1018 patients were included. CSF HIV-RNA was in median (interquartile range [IQR]) 1.03 log10 (0.37–1.86) copies/mL lower than in plasma, and correlated with plasma HIV-RNA (r = 0.44, P < .01), neopterin concentration in CSF (r = 0.49, P < .01) and in serum (r = 0.29, P < .01), CSF WBC (r = 0.34, P < .01) and albumin ratio (r = 0.25, P < .01). CSF HIV-RNA paralleled plasma HIV-RNA in all groups except neuroasymptomatic patients with advanced immunodeficiency (CD4 < 200) and patients with HIV-associated dementia (HAD) or opportunistic central nervous system (CNS) infections. Patients with HAD had the highest CSF HIV-RNA (in median [IQR] 4.73 (3.84–5.35) log10 copies/mL). CSF > plasma discordance was found in 126 of 972 individuals (13%) and varied between groups, from 1% in primary HIV, 11% in neuroasymptomatic groups, up to 30% of patients with HAD. Conclusions Our study confirms previous smaller observations of variations in CSF HIV-RNA in different stages of HIV disease. Overall, CSF HIV-RNA was approximately 1 log10 copies/mL lower in CSF than in plasma, but CSF discordance was found in a substantial minority of subjects, most commonly in patients with HAD, indicating increasing CNS compartmentalization paralleling disease progression.

Funder

Swedish government and county councils

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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