Neurocysticercosis Prevalence and Characteristics in Communities of Sinda District in Zambia: A Cross-Sectional Study.

Taenia solium Cysticercosis Neurocysticercosis Point-of-care test Prevalence Zambia

Journal

Journal of epidemiology and global health
ISSN: 2210-6014
Titre abrégé: J Epidemiol Glob Health
Pays: Switzerland
ID NLM: 101592084

Informations de publication

Date de publication:
09 Jul 2024
Historique:
received: 19 04 2024
accepted: 24 06 2024
medline: 9 7 2024
pubmed: 9 7 2024
entrez: 9 7 2024
Statut: aheadofprint

Résumé

This study aimed at describing the epidemiology of (neuro)cysticercosis as well as its clinical and radiological characteristics in a Taenia solium endemic district of Zambia. This was part of a cross-sectional community-based study conducted in Sinda district to evaluate an antibody-detecting T. solium point-of-care (TS POC) test for taeniosis and (neuro)cysticercosis. All TS POC cysticercosis positive (CC+) participants and a subset of the TS POC cysticercosis negative (CC-) received a clinical evaluation and cerebral computed tomography (CT) examination for neurocysticercosis (NCC) diagnosis and staging. Of the 1249 participants with a valid TS POC test result, 177 (14%) were TS POC CC+ . Cysticercosis sero-prevalence was estimated to be 20.1% (95% confidence intervals [CI] 14.6-27.0%). In total, 233 participants received a CT examination (151 TS POC CC+ , 82 TS POC CC-). Typical NCC lesions were present in 35/151 (23%) TS POC CC+ , and in 10/82 (12%) TS POC CC- participants. NCC prevalence was 13.5% (95% CI 8.4-21.1%) in the study population and 38.0% (95% CI 5.2-87.4%) among people reporting epileptic seizures. Participants with NCC were more likely to experience epileptic seizures (OR = 3.98, 95% CI 1.34-11.78, p = 0.01) than those without NCC, although only 7/45 (16%) people with NCC ever experienced epileptic seizures. The number of lesions did not differ by TS POC CC status (median: 3 [IQR 1-6] versus 2.5 [IQR 1-5.3], p = 0.64). Eight (23%) of the 35 TS POC CC+ participants with NCC had active stage lesions; in contrast none of the TS POC CC- participants was diagnosed with active NCC. NCC is common in communities in the Eastern province of Zambia, but a large proportion of people remain asymptomatic.

Sections du résumé

BACKGROUND BACKGROUND
This study aimed at describing the epidemiology of (neuro)cysticercosis as well as its clinical and radiological characteristics in a Taenia solium endemic district of Zambia.
METHODS METHODS
This was part of a cross-sectional community-based study conducted in Sinda district to evaluate an antibody-detecting T. solium point-of-care (TS POC) test for taeniosis and (neuro)cysticercosis. All TS POC cysticercosis positive (CC+) participants and a subset of the TS POC cysticercosis negative (CC-) received a clinical evaluation and cerebral computed tomography (CT) examination for neurocysticercosis (NCC) diagnosis and staging.
RESULTS RESULTS
Of the 1249 participants with a valid TS POC test result, 177 (14%) were TS POC CC+ . Cysticercosis sero-prevalence was estimated to be 20.1% (95% confidence intervals [CI] 14.6-27.0%). In total, 233 participants received a CT examination (151 TS POC CC+ , 82 TS POC CC-). Typical NCC lesions were present in 35/151 (23%) TS POC CC+ , and in 10/82 (12%) TS POC CC- participants. NCC prevalence was 13.5% (95% CI 8.4-21.1%) in the study population and 38.0% (95% CI 5.2-87.4%) among people reporting epileptic seizures. Participants with NCC were more likely to experience epileptic seizures (OR = 3.98, 95% CI 1.34-11.78, p = 0.01) than those without NCC, although only 7/45 (16%) people with NCC ever experienced epileptic seizures. The number of lesions did not differ by TS POC CC status (median: 3 [IQR 1-6] versus 2.5 [IQR 1-5.3], p = 0.64). Eight (23%) of the 35 TS POC CC+ participants with NCC had active stage lesions; in contrast none of the TS POC CC- participants was diagnosed with active NCC.
CONCLUSION CONCLUSIONS
NCC is common in communities in the Eastern province of Zambia, but a large proportion of people remain asymptomatic.

Identifiants

pubmed: 38980629
doi: 10.1007/s44197-024-00271-z
pii: 10.1007/s44197-024-00271-z
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : European and Developing Countries Clinical Trials Partnership
ID : DRIA2014-308
Organisme : German Federal Ministry of Education and Research
ID : 01KA1617

Informations de copyright

© 2024. The Author(s).

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Auteurs

Gideon Zulu (G)

Ministry of Health, Lusaka, Zambia. gideonzulu@yahoo.com.
Department of Clinical Studies, School of Veterinary Medicine, University of Zambia, Lusaka, Zambia. gideonzulu@yahoo.com.

Dominik Stelzle (D)

Department of Neurology, School of Medicine and Health, Technical University of Munich, Munich, Germany.
Centre for Global Health, School of Medicine and Health, Technical University of Munich, Munich, Germany.

Sarah Gabriël (S)

Department of Translational Physiology, Infectiology and Public Health, Faculty of Veterinary Medicine, Ghent University, Ghent, Belgium.

Chiara Trevisan (C)

Department of Translational Physiology, Infectiology and Public Health, Faculty of Veterinary Medicine, Ghent University, Ghent, Belgium.
Department of Public Health, Institute of Tropical Medicine, Antwerp, Belgium.

Inge Van Damme (I)

Department of Translational Physiology, Infectiology and Public Health, Faculty of Veterinary Medicine, Ghent University, Ghent, Belgium.

Chishimba Mubanga (C)

Department of Clinical Studies, School of Veterinary Medicine, University of Zambia, Lusaka, Zambia.

Veronika Schmidt (V)

Department of Neurology, School of Medicine and Health, Technical University of Munich, Munich, Germany.
Centre for Global Health, School of Medicine and Health, Technical University of Munich, Munich, Germany.

Bernard J Ngowi (BJ)

National Institute for Medical Research, Muhimbili Medical Research Centre, Dar es Salaam, Tanzania.
University of Dar es Salaam, Mbeya College of Health and Allied Sciences, Mbeya, Tanzania.

Tamara M Welte (TM)

Department of Neurology, School of Medicine and Health, Technical University of Munich, Munich, Germany.
Centre for Global Health, School of Medicine and Health, Technical University of Munich, Munich, Germany.
Department of Neurology, Epilepsy Center, University Hospital Erlangen, Erlangen, Germany.

Pascal Magnussen (P)

Department of Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Charlotte Ruether (C)

Department of Radiology, Faculty of Medicine, Technical University of Munich, Munich, Germany.

Agnes Fleury (A)

Instituto de Investigaciones Biomédicas-UNAM/Instituto Nacional de Neurología y Neurocirugía/Facultad de Medicina-UNAM, Mexico City, Mexico.

Pierre Dorny (P)

Department of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Emmanuel Bottieau (E)

Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Isaac K Phiri (IK)

Department of Clinical Studies, School of Veterinary Medicine, University of Zambia, Lusaka, Zambia.

Kabemba E Mwape (KE)

Department of Clinical Studies, School of Veterinary Medicine, University of Zambia, Lusaka, Zambia.

Andrea S Winkler (AS)

Department of Neurology, School of Medicine and Health, Technical University of Munich, Munich, Germany.
Centre for Global Health, School of Medicine and Health, Technical University of Munich, Munich, Germany.
Department of Community Medicine and Global Health, Institute of Health and Society, Faculty of Medicine, University of Oslo, Oslo, Norway.
Department of Global Health and Social Medicine, Harvard Medical School, Boston, MA, USA.

Classifications MeSH