The Presence of Hemoglobin in Cervicovaginal Lavage Is Not Associated With Genital Schistosomiasis in Zambian Women From the BILHIV Study

Author:

Sturt Amy S1ORCID,Webb Emily L2ORCID,Phiri Comfort R3,Mapani Joyce4,Mudenda Maina4,Himschoot Lisa5,Kjetland Eyrun F67,Mweene Tobias3,Levecke Bruno8,van Dam Govert J9,Corstjens Paul L A M10,Ayles Helen311,Hayes Richard J2,Francis Suzanna C2,van Lieshout Lisette9,Cools Piet58,Hansingo Isaiah4,Bustinduy Amaya L11

Affiliation:

1. Department of Infectious Diseases, Veterans Affairs Health Care System , Palo Alto, California , USA

2. MRC International Statistics and Epidemiology Group, London School of Hygiene and Tropical Medicine , London , United Kingdom

3. Zambart , Lusaka , Zambia

4. Department of Obstetrics and Gynecology, Livingstone Central Hospital , Livingstone , Zambia

5. Department of Diagnostic Sciences, Faculty of Medicine and Health Sciences, Ghent University , Ghent , Belgium

6. Department of Infectious Diseases and Global Health, Norwegian Centre for Imported and Tropical Diseases, Oslo University Hospital , Oslo , Norway

7. Discipline of Public Health Medicine, College of Health Sciences, University of Kwa-Zulu Natal , Durban , South Africa

8. Department of Translational Physiology, Infectiology and Public Health, Ghent University , Merelbeke , Belgium

9. Department of Parasitology, Leiden University Medical Center , Leiden , The Netherlands

10. Department of Cell and Chemical Biology, Leiden University Medical Center , Leiden , The Netherlands

11. Department of Clinical Research, London School of Hygiene and Tropical Medicine , London , United Kingdom

Abstract

Abstract Background Female genital schistosomiasis (FGS) occurs when Schistosoma haematobium eggs are deposited in reproductive tissue. Female genital schistosomiasis in the cervical mucosa is associated with increased vascularity. If FGS is associated with the presence of hemoglobin in cervicovaginal lavage (CVL), the use of urinary reagent strips to detect hemoglobin in CVL could supplement FGS diagnosis. Methods Nonmenstruating, nonpregnant, sexually active women aged 18–31 participating in the HPTN 071 (PopART) Population-Cohort were invited in 2 Zambian communities. Genital self-swabs and a urine specimen were collected at a home visit, and CVL and hand-held colposcopy were performed at a midwife led clinic visit. Urinary reagent strips were used to identify hemoglobin in CVL. Eggs and circulating anodic antigen (CAA) were detected from urine. Visual-FGS was defined as the presence of sandy patches, rubbery papules, or abnormal blood vessels. Polymerase chain reaction (PCR)-FGS was defined as Schistosoma deoxyribonucleic acid detected by real-time PCR on CVL or cervical or vaginal swab. Results Of 209 women with home genital swabs and companion CVL specimens, 66% (138 of 209) had detectable CVL hemoglobin, 13.4% (28 of 209) had PCR-defined FGS, and 17.2% (36 of 209) had visual-FGS. Active Schistosoma infection, diagnosed by CAA or urine microscopy, was present in 21.0% (44 of 209) participants. Active Schistosoma infection (P = .4), PCR-FGS (P = 0.7), and visual-FGS (P = 0.3) were not associated with CVL hemoglobin presence. Results did not differ in subgroups with high infection burden (cycle threshold < 35 or 2–3 positive genital PCR). Conclusions Polymerase chain reaction-FGS, visual-FGS, and active Schistosoma infection were not associated with the presence of CVL hemoglobin. Further research is needed to establish accessible community-based FGS diagnostics.

Funder

Wellcome Trust

Research Foundation—Flanders

Bill & Melinda Gates Foundation Project

MRC

UK Medical Research Council

DFID Concordat agreement

EDCTP2 program

European Union

National Institute of Allergy and Infectious Diseases

U.S. President’s Emergency Plan for AIDS Relief

International Initiative for Impact Evaluation

Bill & Melinda Gates Foundation

NIAID, the National Institute on Drug Abuse

National Institutes of Health

South-Eastern Regional Health Authority

Norway

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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