A national survey integrating clinical, laboratory, and WASH data to determine the typology of trachoma in Nauru.


Journal

PLoS neglected tropical diseases
ISSN: 1935-2735
Titre abrégé: PLoS Negl Trop Dis
Pays: United States
ID NLM: 101291488

Informations de publication

Date de publication:
04 2022
Historique:
received: 03 09 2021
accepted: 24 02 2022
entrez: 19 4 2022
pubmed: 20 4 2022
medline: 22 4 2022
Statut: epublish

Résumé

The epidemiology of trachoma in several Pacific Islands differs from other endemic settings, in that there is a high prevalence of clinical signs of trachoma, particularly trachomatous inflammation-follicular (TF), but few cases of trichiasis and limited evidence of ocular chlamydial infection. This so-called "Pacific enigma" has led to uncertainty regarding the appropriate public health response. In 2019 alongside Nauru's national trachoma population survey, we performed bacteriological and serological assessments of children to better understand the typology of trachoma and to determine whether there is a need for trachoma interventions. We used two-stage cluster sampling, examining residents aged ≥1 year and collecting household-level water, sanitation, and hygiene (WASH) variables. Children aged 1-9 years provided conjunctival swabs and finger-prick dried blood spots to investigate the presence of Chlamydia trachomatis nucleic acid and anti-Pgp3 antibodies, respectively. In 818 participants aged 1-9 years, the age-adjusted TF prevalence was 21.8% (95% CI 15.2-26.2%); ocular C. trachomatis prevalence was 34.5% (95% CI 30.6-38.9), and anti-Pgp3 antibody prevalence was 32.1% (95% CI 28.4%-36.3%). The age- and gender-adjusted prevalence of trichiasis in ≥15-year-olds was 0.3% (95% CI 0.00-0.85), but no individual with trichiasis had trachomatous scarring (TS). Multivariable analysis showed an association between age and both TF (OR per year of age 1.3 [95% CI 1.2-1.4]) and anti-Pgp3 positivity (OR 1.2 [95% CI 1.2-1.3]). There were high rates of access to water and sanitation and no WASH variable was associated with the presence of TF. TF, nucleic acid, and age-specific antibody prevalence collectively indicate that high levels of C. trachomatis transmission among children present a high risk of ocular damage due to trachoma. The absence of trichiasis with trachomatous scarring suggest a relatively recent increase in transmission intensity.

Sections du résumé

BACKGROUND
The epidemiology of trachoma in several Pacific Islands differs from other endemic settings, in that there is a high prevalence of clinical signs of trachoma, particularly trachomatous inflammation-follicular (TF), but few cases of trichiasis and limited evidence of ocular chlamydial infection. This so-called "Pacific enigma" has led to uncertainty regarding the appropriate public health response. In 2019 alongside Nauru's national trachoma population survey, we performed bacteriological and serological assessments of children to better understand the typology of trachoma and to determine whether there is a need for trachoma interventions.
METHODS
We used two-stage cluster sampling, examining residents aged ≥1 year and collecting household-level water, sanitation, and hygiene (WASH) variables. Children aged 1-9 years provided conjunctival swabs and finger-prick dried blood spots to investigate the presence of Chlamydia trachomatis nucleic acid and anti-Pgp3 antibodies, respectively.
PRINCIPAL FINDINGS
In 818 participants aged 1-9 years, the age-adjusted TF prevalence was 21.8% (95% CI 15.2-26.2%); ocular C. trachomatis prevalence was 34.5% (95% CI 30.6-38.9), and anti-Pgp3 antibody prevalence was 32.1% (95% CI 28.4%-36.3%). The age- and gender-adjusted prevalence of trichiasis in ≥15-year-olds was 0.3% (95% CI 0.00-0.85), but no individual with trichiasis had trachomatous scarring (TS). Multivariable analysis showed an association between age and both TF (OR per year of age 1.3 [95% CI 1.2-1.4]) and anti-Pgp3 positivity (OR 1.2 [95% CI 1.2-1.3]). There were high rates of access to water and sanitation and no WASH variable was associated with the presence of TF.
CONCLUSIONS
TF, nucleic acid, and age-specific antibody prevalence collectively indicate that high levels of C. trachomatis transmission among children present a high risk of ocular damage due to trachoma. The absence of trichiasis with trachomatous scarring suggest a relatively recent increase in transmission intensity.

Identifiants

pubmed: 35439248
doi: 10.1371/journal.pntd.0010275
pii: PNTD-D-21-01312
pmc: PMC9017947
doi:

Substances chimiques

Nucleic Acids 0
Water 059QF0KO0R

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0010275

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

Déclaration de conflit d'intérêts

I have read the journal’s policy and the authors of this manuscript have the following competing interests: AB is employed by the International Trachoma Initiative at The Task Force for Global Health, which receives an operating budget and research funds from Pfizer Inc., the manufacturers of Zithromax (azithromycin). EMHE receives salary support from the International Trachoma Initiative.

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Auteurs

Kathleen D Lynch (KD)

UQ Centre for Clinical Research, University of Queensland, Brisbane, Australia.

Sue Chen Apadinuwe (SC)

Ministry of Health and Medical Services, Denig, Republic of Nauru.

Stephen B Lambert (SB)

UQ Centre for Clinical Research, University of Queensland, Brisbane, Australia.
National Centre for Immunisation Research and Surveillance, Westmead, New South Wales, Australia.

Tessa Hillgrove (T)

The Fred Hollows Foundation, Melbourne, Australia.

Mitchell Starr (M)

NSW State Reference Laboratory for HIV, St Vincent's Centre for Applied Medical Research, St Vincent's Hospital, Sydney, Australia.

Beth Catlett (B)

NSW State Reference Laboratory for HIV, St Vincent's Centre for Applied Medical Research, St Vincent's Hospital, Sydney, Australia.

Robert S Ware (RS)

Menzies Health Institute Queensland and School of Medicine, Griffith University, Brisbane, Australia.

Anasaini Cama (A)

The Fred Hollows Foundation, Melbourne, Australia.

Sara Webster (S)

The Fred Hollows Foundation, Melbourne, Australia.

Emma M Harding-Esch (EM)

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

Ana Bakhtiari (A)

International Trachoma Initiative, Task Force for Global Health, Decatur, Georgia, United States of America.

Robert Butcher (R)

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

Philip Cunningham (P)

NSW State Reference Laboratory for HIV, St Vincent's Centre for Applied Medical Research, St Vincent's Hospital, Sydney, Australia.

Diana Martin (D)

Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Sarah Gwyn (S)

Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Anthony W Solomon (AW)

Department of Control of Neglected Tropical Diseases, World Health Organization, Geneva, Switzerland.

Chandalene Garabwan (C)

Ministry of Health and Medical Services, Denig, Republic of Nauru.

John M Kaldor (JM)

The Kirby Institute, University of New South Wales, Sydney, Australia.

Susana Vaz Nery (S)

The Kirby Institute, University of New South Wales, Sydney, Australia.

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Classifications MeSH