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Low prevalence of symptomatic thyroid diseases and thyroid cancers in HIV-infected patients
Thyroid diseases (TDs) have been widely associated with HIV infection. However, data about TDs prevalence and distribution are controversial, and few published studies are available. The aim of our study was to assess prevalence and risk factors of symptomatic thyroid disturbances, including thyroid...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6923431/ https://www.ncbi.nlm.nih.gov/pubmed/31857648 http://dx.doi.org/10.1038/s41598-019-56032-7 |
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author | Properzi, Martina della Giustina, Tommaso Mentasti, Sara Castelli, Francesco Chiesa, Annacarla Gregori, Natalia Quiros-Roldan, Eugenia |
author_facet | Properzi, Martina della Giustina, Tommaso Mentasti, Sara Castelli, Francesco Chiesa, Annacarla Gregori, Natalia Quiros-Roldan, Eugenia |
author_sort | Properzi, Martina |
collection | PubMed |
description | Thyroid diseases (TDs) have been widely associated with HIV infection. However, data about TDs prevalence and distribution are controversial, and few published studies are available. The aim of our study was to assess prevalence and risk factors of symptomatic thyroid disturbances, including thyroid cancers, in a large cohort of HIV-infected patients. A retrospective cohort study was performed at the Department of Infectious and Tropical Diseases of the University of Brescia, Italy, in the period 2005–2017. We identified all HIV-positive patients with a diagnosis of symptomatic TD in the electronic database of our Department (HIVeDB); we also operated a record-linkage between our data and the Health Protection Agency database (HPADB) of Brescia Province. Multivariate logistic regression analysis was used to determine risk factors associated with TDs onset; an incidence rate analysis was also performed. During the study period, 6343 HIV-infected patients have been followed at our Department; 123 received a diagnosis of symptomatic TD (1.94% of the entire cohort). In the TDs group, almost half of patients were females (n = 59, 48%), mean age was 47.15 years (SD: 11.56). At TD diagnosis, mean T CD4+ cell count was 491 cell/uL and most patients showed undetectable HIV-RNA (n = 117, 95.12%). Among them, 81 patients were found to have hypothyroidism (63 with Hashimoto’s thyroiditis), 21 hyperthyroidism (17 suffered from Graves’ disease), while 11 subjects were diagnosed with a primitive thyroid cancer. Papillary thyroid cancer was the most frequent histotype (n = 7, 63.63%), followed by medullary (n = 2, 18.18%) and follicular thyroid cancer (n = 1, 9.1%). Male gender was a protective factor for TDs development, especially for hypothyroidism (p < 0.001); age emerged as a variable associated with both hypothyroidism (p = 0.03) and thyroid cancer (p = 0.03), while CD4+ cell nadir <200 cell/mm(3) was associated with symptomatic hyperthyroidism (p = 0.005). To conclude, symptomatic thyroid dysfunctions rate in well-treated HIV-infected patients is low. Age and gender are crucial elements in the onset of thyroid abnormalities, together with T CD4+ cell nadir. Interestingly, medullary thyroid cancer seems to be much more frequent in HIV-infected patients compared to the general population. |
format | Online Article Text |
id | pubmed-6923431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69234312019-12-20 Low prevalence of symptomatic thyroid diseases and thyroid cancers in HIV-infected patients Properzi, Martina della Giustina, Tommaso Mentasti, Sara Castelli, Francesco Chiesa, Annacarla Gregori, Natalia Quiros-Roldan, Eugenia Sci Rep Article Thyroid diseases (TDs) have been widely associated with HIV infection. However, data about TDs prevalence and distribution are controversial, and few published studies are available. The aim of our study was to assess prevalence and risk factors of symptomatic thyroid disturbances, including thyroid cancers, in a large cohort of HIV-infected patients. A retrospective cohort study was performed at the Department of Infectious and Tropical Diseases of the University of Brescia, Italy, in the period 2005–2017. We identified all HIV-positive patients with a diagnosis of symptomatic TD in the electronic database of our Department (HIVeDB); we also operated a record-linkage between our data and the Health Protection Agency database (HPADB) of Brescia Province. Multivariate logistic regression analysis was used to determine risk factors associated with TDs onset; an incidence rate analysis was also performed. During the study period, 6343 HIV-infected patients have been followed at our Department; 123 received a diagnosis of symptomatic TD (1.94% of the entire cohort). In the TDs group, almost half of patients were females (n = 59, 48%), mean age was 47.15 years (SD: 11.56). At TD diagnosis, mean T CD4+ cell count was 491 cell/uL and most patients showed undetectable HIV-RNA (n = 117, 95.12%). Among them, 81 patients were found to have hypothyroidism (63 with Hashimoto’s thyroiditis), 21 hyperthyroidism (17 suffered from Graves’ disease), while 11 subjects were diagnosed with a primitive thyroid cancer. Papillary thyroid cancer was the most frequent histotype (n = 7, 63.63%), followed by medullary (n = 2, 18.18%) and follicular thyroid cancer (n = 1, 9.1%). Male gender was a protective factor for TDs development, especially for hypothyroidism (p < 0.001); age emerged as a variable associated with both hypothyroidism (p = 0.03) and thyroid cancer (p = 0.03), while CD4+ cell nadir <200 cell/mm(3) was associated with symptomatic hyperthyroidism (p = 0.005). To conclude, symptomatic thyroid dysfunctions rate in well-treated HIV-infected patients is low. Age and gender are crucial elements in the onset of thyroid abnormalities, together with T CD4+ cell nadir. Interestingly, medullary thyroid cancer seems to be much more frequent in HIV-infected patients compared to the general population. Nature Publishing Group UK 2019-12-19 /pmc/articles/PMC6923431/ /pubmed/31857648 http://dx.doi.org/10.1038/s41598-019-56032-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Properzi, Martina della Giustina, Tommaso Mentasti, Sara Castelli, Francesco Chiesa, Annacarla Gregori, Natalia Quiros-Roldan, Eugenia Low prevalence of symptomatic thyroid diseases and thyroid cancers in HIV-infected patients |
title | Low prevalence of symptomatic thyroid diseases and thyroid cancers in HIV-infected patients |
title_full | Low prevalence of symptomatic thyroid diseases and thyroid cancers in HIV-infected patients |
title_fullStr | Low prevalence of symptomatic thyroid diseases and thyroid cancers in HIV-infected patients |
title_full_unstemmed | Low prevalence of symptomatic thyroid diseases and thyroid cancers in HIV-infected patients |
title_short | Low prevalence of symptomatic thyroid diseases and thyroid cancers in HIV-infected patients |
title_sort | low prevalence of symptomatic thyroid diseases and thyroid cancers in hiv-infected patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6923431/ https://www.ncbi.nlm.nih.gov/pubmed/31857648 http://dx.doi.org/10.1038/s41598-019-56032-7 |
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