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Incidence of depression in patients with hepatitis C treated with direct-acting antivirals
OBJECTIVE: Depression has been associated with hepatitis C, as well as with its treatment with proinflammatory cytokines (i.e., interferon). The new direct-acting antiviral agents (DAAs) have minimal adverse effects and high potency, with a direct inhibitory effect on non-structural viral proteins....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação Brasileira de Psiquiatria
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986477/ https://www.ncbi.nlm.nih.gov/pubmed/31314868 http://dx.doi.org/10.1590/1516-4446-2018-0336 |
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author | Egmond, Elfi Mariño, Zoe Navines, Ricard Oriolo, Giovanni Pla, Anna Bartres, Concepció Lens, Sabela Forns, Xavier Martin-Santos, Rocio |
author_facet | Egmond, Elfi Mariño, Zoe Navines, Ricard Oriolo, Giovanni Pla, Anna Bartres, Concepció Lens, Sabela Forns, Xavier Martin-Santos, Rocio |
author_sort | Egmond, Elfi |
collection | PubMed |
description | OBJECTIVE: Depression has been associated with hepatitis C, as well as with its treatment with proinflammatory cytokines (i.e., interferon). The new direct-acting antiviral agents (DAAs) have minimal adverse effects and high potency, with a direct inhibitory effect on non-structural viral proteins. We studied the incidence and associated factors of depression in a real-life prospective cohort of chronic hepatitis C patients treated with the new DAAs. METHODS: The sample was recruited from a cohort of 91 patients with hepatitis C, of both sexes, with advanced level of fibrosis and no HIV coinfection, consecutively enrolled during a 6-month period for DAA treatment; those euthymic at baseline (n=54) were selected. All were evaluated through the depression module of the Patient Health Questionnaire (PHQ-9-DSM-IV), at three time points: baseline, 4 weeks, and end-of-treatment. RESULTS: The cumulative incidence (95%CI) of major depression and any depressive disorder during DAA treatment was 13% (6.4-24.4) and 46.3% (33.7-59.4), respectively. No differences were observed between those patients with and without cirrhosis or ribavirin treatment (p > 0.05). Risk factors for incident major depression during DAA treatment included family depression (relative risk 9.1 [1.62-51.1]), substance use disorder (11.0 [1.7-73.5]), and baseline PHQ-9 score (2.1 [1.1-3.1]). CONCLUSIONS: The findings of this study highlight the importance of screening for new depression among patients receiving new DAAs, and identify potential associated risk factors. |
format | Online Article Text |
id | pubmed-6986477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Associação Brasileira de Psiquiatria |
record_format | MEDLINE/PubMed |
spelling | pubmed-69864772020-01-29 Incidence of depression in patients with hepatitis C treated with direct-acting antivirals Egmond, Elfi Mariño, Zoe Navines, Ricard Oriolo, Giovanni Pla, Anna Bartres, Concepció Lens, Sabela Forns, Xavier Martin-Santos, Rocio Braz J Psychiatry Brief Communication OBJECTIVE: Depression has been associated with hepatitis C, as well as with its treatment with proinflammatory cytokines (i.e., interferon). The new direct-acting antiviral agents (DAAs) have minimal adverse effects and high potency, with a direct inhibitory effect on non-structural viral proteins. We studied the incidence and associated factors of depression in a real-life prospective cohort of chronic hepatitis C patients treated with the new DAAs. METHODS: The sample was recruited from a cohort of 91 patients with hepatitis C, of both sexes, with advanced level of fibrosis and no HIV coinfection, consecutively enrolled during a 6-month period for DAA treatment; those euthymic at baseline (n=54) were selected. All were evaluated through the depression module of the Patient Health Questionnaire (PHQ-9-DSM-IV), at three time points: baseline, 4 weeks, and end-of-treatment. RESULTS: The cumulative incidence (95%CI) of major depression and any depressive disorder during DAA treatment was 13% (6.4-24.4) and 46.3% (33.7-59.4), respectively. No differences were observed between those patients with and without cirrhosis or ribavirin treatment (p > 0.05). Risk factors for incident major depression during DAA treatment included family depression (relative risk 9.1 [1.62-51.1]), substance use disorder (11.0 [1.7-73.5]), and baseline PHQ-9 score (2.1 [1.1-3.1]). CONCLUSIONS: The findings of this study highlight the importance of screening for new depression among patients receiving new DAAs, and identify potential associated risk factors. Associação Brasileira de Psiquiatria 2019-07-15 /pmc/articles/PMC6986477/ /pubmed/31314868 http://dx.doi.org/10.1590/1516-4446-2018-0336 Text en http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Brief Communication Egmond, Elfi Mariño, Zoe Navines, Ricard Oriolo, Giovanni Pla, Anna Bartres, Concepció Lens, Sabela Forns, Xavier Martin-Santos, Rocio Incidence of depression in patients with hepatitis C treated with direct-acting antivirals |
title | Incidence of depression in patients with hepatitis C treated with direct-acting antivirals |
title_full | Incidence of depression in patients with hepatitis C treated with direct-acting antivirals |
title_fullStr | Incidence of depression in patients with hepatitis C treated with direct-acting antivirals |
title_full_unstemmed | Incidence of depression in patients with hepatitis C treated with direct-acting antivirals |
title_short | Incidence of depression in patients with hepatitis C treated with direct-acting antivirals |
title_sort | incidence of depression in patients with hepatitis c treated with direct-acting antivirals |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986477/ https://www.ncbi.nlm.nih.gov/pubmed/31314868 http://dx.doi.org/10.1590/1516-4446-2018-0336 |
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