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Evaluation of Fecal Inflammatory Biomarkers to Identify Bacterial Diarrhea Episodes: Systematic Review and Protocol for the Enterics for Global Health Shigella Surveillance Study.
Babb, Courtney; Badji, Henry; Bhuiyan, Md Taufiqur Rahman; Cornick, Jennifer; Qureshi, Sonia; Sonye, Catherine; Shapiama Lopez, Wagner V; Adnan, Mehreen; Atlas, Hannah E; Begum, Kehkashan; Brennhofer, Stephanie A; Ceesay, Bubacarr E; Ceesay, Abdoulie K; Cunliffe, Nigel A; Garcia Bardales, Paul F; Haque, Shahinur; Horne, Bri'Anna; Hossain, M Jahangir; Iqbal, Junaid; Islam, Md Taufiqul; Islam, Sadia; Khanam, Farhana; Kotloff, Karen L; Malemia, Thandizo; Manzanares Villanueva, Katia; Million, Gertrude Malola; Munthali, Vitumbiko; Ochieng, John Benjamin; Ogwel, Billy; Paredes Olortegui, Maribel; Omore, Richard; Pavlinac, Patricia B; Platts-Mills, James A; Sears, Khandra T; Secka, Ousman; Tennant, Sharon M; Peñataro Yori, Pablo; Yousafzai, Mohammad Tahir; Jere, Khuzwayo C; Kosek, Margaret N; Munga, Stephen; Ikumapayi, Usman N; Qadri, Firdausi; Qamar, Farah Naz; Rogawski McQuade, Elizabeth T.
Afiliación
  • Babb C; Department of Epidemiology, Emory University, Atlanta, Georgia, USA.
  • Badji H; Medical Research Council Unit The Gambia, London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
  • Bhuiyan MTR; Infectious Diseases Division, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Cornick J; Institute of Infection, Veterinary and Ecological Sciences, Department of Clinical Infection, Microbiology and Immunology, University of Liverpool, Liverpool, United Kingdom.
  • Qureshi S; Malawi Liverpool Wellcome Programme, Blantyre, Malawi.
  • Sonye C; Department of Pediatrics and Child Health, The Aga Khan University, Karachi, Pakistan.
  • Shapiama Lopez WV; Center for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
  • Adnan M; Asociación Benéfica PRISMA, Iquitos, Peru.
  • Atlas HE; Department of Pediatrics and Child Health, The Aga Khan University, Karachi, Pakistan.
  • Begum K; Department of Global Health, University of Washington, Seattle, Washington, USA.
  • Brennhofer SA; Department of Pediatrics and Child Health, The Aga Khan University, Karachi, Pakistan.
  • Ceesay BE; Division of Infectious Diseases and International Health, University of Virginia, Charlottesville, Virginia, USA.
  • Ceesay AK; Medical Research Council Unit The Gambia, London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
  • Cunliffe NA; Medical Research Council Unit The Gambia, London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
  • Garcia Bardales PF; Institute of Infection, Veterinary and Ecological Sciences, Department of Clinical Infection, Microbiology and Immunology, University of Liverpool, Liverpool, United Kingdom.
  • Haque S; Asociación Benéfica PRISMA, Iquitos, Peru.
  • Horne B; Infectious Diseases Division, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Hossain MJ; Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Iqbal J; Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Islam MT; Medical Research Council Unit The Gambia, London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
  • Islam S; Department of Pediatrics and Child Health, The Aga Khan University, Karachi, Pakistan.
  • Khanam F; Infectious Diseases Division, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Kotloff KL; Infectious Diseases Division, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Malemia T; Infectious Diseases Division, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Manzanares Villanueva K; Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Million GM; Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Munthali V; Malawi Liverpool Wellcome Programme, Blantyre, Malawi.
  • Ochieng JB; Asociación Benéfica PRISMA, Iquitos, Peru.
  • Ogwel B; Malawi Liverpool Wellcome Programme, Blantyre, Malawi.
  • Paredes Olortegui M; Malawi Liverpool Wellcome Programme, Blantyre, Malawi.
  • Omore R; Center for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
  • Pavlinac PB; Center for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
  • Platts-Mills JA; Asociación Benéfica PRISMA, Iquitos, Peru.
  • Sears KT; Center for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
  • Secka O; Department of Global Health, University of Washington, Seattle, Washington, USA.
  • Tennant SM; Division of Infectious Diseases and International Health, University of Virginia, Charlottesville, Virginia, USA.
  • Peñataro Yori P; Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Yousafzai MT; Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Jere KC; Medical Research Council Unit The Gambia, London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
  • Kosek MN; Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Munga S; Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Ikumapayi UN; Division of Infectious Diseases and International Health, University of Virginia, Charlottesville, Virginia, USA.
  • Qadri F; Department of Pediatrics and Child Health, The Aga Khan University, Karachi, Pakistan.
  • Qamar FN; Institute of Infection, Veterinary and Ecological Sciences, Department of Clinical Infection, Microbiology and Immunology, University of Liverpool, Liverpool, United Kingdom.
  • Rogawski McQuade ET; Malawi Liverpool Wellcome Programme, Blantyre, Malawi.
Open Forum Infect Dis ; 11(Suppl 1): S65-S75, 2024 Mar.
Article en En | MEDLINE | ID: mdl-38532957
ABSTRACT

Background:

The measurement of fecal inflammatory biomarkers among individuals presenting to care with diarrhea could improve the identification of bacterial diarrheal episodes that would benefit from antibiotic therapy. We reviewed prior literature in this area and describe our proposed methods to evaluate 4 biomarkers in the Enterics for Global Health (EFGH) Shigella surveillance study.

Methods:

We systematically reviewed studies since 1970 from PubMed and Embase that assessed the diagnostic characteristics of inflammatory biomarkers to identify bacterial diarrhea episodes. We extracted sensitivity and specificity and summarized the evidence by biomarker and diarrhea etiology. In EFGH, we propose using commercial enzyme-linked immunosorbent assays to test for myeloperoxidase, calprotectin, lipocalin-2, and hemoglobin in stored whole stool samples collected within 24 hours of enrollment from participants in the Bangladesh, Kenya, Malawi, Pakistan, Peru, and The Gambia sites. We will develop clinical prediction scores that incorporate the inflammatory biomarkers and evaluate their ability to identify Shigella and other bacterial etiologies of diarrhea as determined by quantitative polymerase chain reaction (qPCR).

Results:

Forty-nine studies that assessed fecal leukocytes (n = 39), red blood cells (n = 26), lactoferrin (n = 13), calprotectin (n = 8), and myeloperoxidase (n = 1) were included in the systematic review. Sensitivities were high for identifying Shigella, moderate for identifying any bacteria, and comparable across biomarkers. Specificities varied depending on the outcomes assessed. Prior studies were generally small, identified red and white blood cells by microscopy, and used insensitive gold standard diagnostics, such as conventional bacteriological culture for pathogen detection.

Conclusions:

Our evaluation of inflammatory biomarkers to distinguish diarrhea etiologies as determined by qPCR will provide an important addition to the prior literature, which was likely biased by the limited sensitivity of the gold standard diagnostics used. We will determine whether point-of-care biomarker tests could be a viable strategy to inform treatment decision making and increase appropriate targeting of antibiotic treatment to bacterial diarrhea episodes.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Open Forum Infect Dis Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Open Forum Infect Dis Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos