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Estimating age-dependent per-encounter chlamydia trachomatis acquisition risk via a Markov-based state-transition model
BACKGROUND: Chlamydial infection is a common bacterial sexually transmitted infection worldwide, caused by C. trachomatis. The screening for C. trachomatis has been proven to be successful. However, such success is not fully realized through tailoring the recommended screening strategies for differe...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022339/ https://www.ncbi.nlm.nih.gov/pubmed/24872872 http://dx.doi.org/10.1186/2043-9113-4-7 |
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author | Teng, Yu Kong, Nan Tu, Wanzhu |
author_facet | Teng, Yu Kong, Nan Tu, Wanzhu |
author_sort | Teng, Yu |
collection | PubMed |
description | BACKGROUND: Chlamydial infection is a common bacterial sexually transmitted infection worldwide, caused by C. trachomatis. The screening for C. trachomatis has been proven to be successful. However, such success is not fully realized through tailoring the recommended screening strategies for different age groups. This is partly due to the knowledge gap in understanding how the infection is correlated with age. In this paper, we estimate age-dependent risks of acquiring C. trachomatis by adolescent women via unprotected heterosexual acts. METHODS: We develop a time-varying Markov state-transition model and compute the incidences of chlamydial infection at discrete age points by simulating the state-transition model with candidate per-encounter acquisition risks and sampled numbers of unit-time unprotected coital events at different age points. We solve an optimization problem to identify the age-dependent estimates that offer the closest matches to the observed infection incidences. We also investigate the impact of antimicrobial treatment effectiveness on the parameter estimates and the differences between the acquisition risks for the first-time infections and repeated infections. RESULTS: Our case study supports the beliefs that age is an inverse predictor of C. trachomatis transmission and that protective immunity developed after initial infection is only partial. CONCLUSIONS: Our modeling method offers a flexible and expandable platform for investigating STI transmission. |
format | Online Article Text |
id | pubmed-4022339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40223392014-05-28 Estimating age-dependent per-encounter chlamydia trachomatis acquisition risk via a Markov-based state-transition model Teng, Yu Kong, Nan Tu, Wanzhu J Clin Bioinforma Research BACKGROUND: Chlamydial infection is a common bacterial sexually transmitted infection worldwide, caused by C. trachomatis. The screening for C. trachomatis has been proven to be successful. However, such success is not fully realized through tailoring the recommended screening strategies for different age groups. This is partly due to the knowledge gap in understanding how the infection is correlated with age. In this paper, we estimate age-dependent risks of acquiring C. trachomatis by adolescent women via unprotected heterosexual acts. METHODS: We develop a time-varying Markov state-transition model and compute the incidences of chlamydial infection at discrete age points by simulating the state-transition model with candidate per-encounter acquisition risks and sampled numbers of unit-time unprotected coital events at different age points. We solve an optimization problem to identify the age-dependent estimates that offer the closest matches to the observed infection incidences. We also investigate the impact of antimicrobial treatment effectiveness on the parameter estimates and the differences between the acquisition risks for the first-time infections and repeated infections. RESULTS: Our case study supports the beliefs that age is an inverse predictor of C. trachomatis transmission and that protective immunity developed after initial infection is only partial. CONCLUSIONS: Our modeling method offers a flexible and expandable platform for investigating STI transmission. BioMed Central 2014-04-25 /pmc/articles/PMC4022339/ /pubmed/24872872 http://dx.doi.org/10.1186/2043-9113-4-7 Text en Copyright © 2014 Teng et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Research Teng, Yu Kong, Nan Tu, Wanzhu Estimating age-dependent per-encounter chlamydia trachomatis acquisition risk via a Markov-based state-transition model |
title | Estimating age-dependent per-encounter chlamydia trachomatis acquisition risk via a Markov-based state-transition model |
title_full | Estimating age-dependent per-encounter chlamydia trachomatis acquisition risk via a Markov-based state-transition model |
title_fullStr | Estimating age-dependent per-encounter chlamydia trachomatis acquisition risk via a Markov-based state-transition model |
title_full_unstemmed | Estimating age-dependent per-encounter chlamydia trachomatis acquisition risk via a Markov-based state-transition model |
title_short | Estimating age-dependent per-encounter chlamydia trachomatis acquisition risk via a Markov-based state-transition model |
title_sort | estimating age-dependent per-encounter chlamydia trachomatis acquisition risk via a markov-based state-transition model |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022339/ https://www.ncbi.nlm.nih.gov/pubmed/24872872 http://dx.doi.org/10.1186/2043-9113-4-7 |
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