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Vildagliptin-induced acute lung injury: a case report

BACKGROUND: Dipeptidyl peptidase-4 inhibitors are a class of oral hypoglycemic drugs and are used widely to treat type 2 diabetes mellitus in many countries. Adverse effects include nasopharyngitis, headache, elevated serum pancreatic enzymes, and gastrointestinal symptoms. In addition, a few cases...

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Autores principales: Ohara, Nobumasa, Kaneko, Masanori, Sato, Kazuhiro, Maruyama, Ryoko, Furukawa, Tomoyasu, Tanaka, Junta, Kaneko, Kenzo, Kamoi, Kyuzi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4983085/
https://www.ncbi.nlm.nih.gov/pubmed/27520566
http://dx.doi.org/10.1186/s13256-016-1006-4
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author Ohara, Nobumasa
Kaneko, Masanori
Sato, Kazuhiro
Maruyama, Ryoko
Furukawa, Tomoyasu
Tanaka, Junta
Kaneko, Kenzo
Kamoi, Kyuzi
author_facet Ohara, Nobumasa
Kaneko, Masanori
Sato, Kazuhiro
Maruyama, Ryoko
Furukawa, Tomoyasu
Tanaka, Junta
Kaneko, Kenzo
Kamoi, Kyuzi
author_sort Ohara, Nobumasa
collection PubMed
description BACKGROUND: Dipeptidyl peptidase-4 inhibitors are a class of oral hypoglycemic drugs and are used widely to treat type 2 diabetes mellitus in many countries. Adverse effects include nasopharyngitis, headache, elevated serum pancreatic enzymes, and gastrointestinal symptoms. In addition, a few cases of interstitial pneumonia associated with their use have been reported in the Japanese literature. Here we describe a patient who developed drug-induced acute lung injury shortly after the administration of the dipeptidyl peptidase-4 inhibitor vildagliptin. CASE PRESENTATION: A 38-year-old Japanese woman with diabetes mellitus developed acute respiratory failure 1 day after administration of vildagliptin. Chest computed tomography revealed nonsegmental ground-glass opacities in her lungs. There was no evidence of bacterial pneumonia or any other cause of her respiratory manifestations. After discontinuation of vildagliptin, she recovered fully from her respiratory disorder. She received insulin therapy for her diabetes mellitus, and her subsequent clinical course has been uneventful. CONCLUSIONS: The period of drug exposure in previously reported cases of patients with drug-induced interstitial pneumonia caused by dipeptidyl peptidase-4 inhibitor varied from several days to over 6 months. In the present case, our patient developed interstitial pneumonia only 1 day after the administration of vildagliptin. The precise mechanism of her vildagliptin-induced lung injury remains uncertain, but physicians should consider that dipeptidyl peptidase-4 inhibitor-induced lung injury, although rare, may appear acutely, even within days after administration of this drug.
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spelling pubmed-49830852016-08-14 Vildagliptin-induced acute lung injury: a case report Ohara, Nobumasa Kaneko, Masanori Sato, Kazuhiro Maruyama, Ryoko Furukawa, Tomoyasu Tanaka, Junta Kaneko, Kenzo Kamoi, Kyuzi J Med Case Rep Case Report BACKGROUND: Dipeptidyl peptidase-4 inhibitors are a class of oral hypoglycemic drugs and are used widely to treat type 2 diabetes mellitus in many countries. Adverse effects include nasopharyngitis, headache, elevated serum pancreatic enzymes, and gastrointestinal symptoms. In addition, a few cases of interstitial pneumonia associated with their use have been reported in the Japanese literature. Here we describe a patient who developed drug-induced acute lung injury shortly after the administration of the dipeptidyl peptidase-4 inhibitor vildagliptin. CASE PRESENTATION: A 38-year-old Japanese woman with diabetes mellitus developed acute respiratory failure 1 day after administration of vildagliptin. Chest computed tomography revealed nonsegmental ground-glass opacities in her lungs. There was no evidence of bacterial pneumonia or any other cause of her respiratory manifestations. After discontinuation of vildagliptin, she recovered fully from her respiratory disorder. She received insulin therapy for her diabetes mellitus, and her subsequent clinical course has been uneventful. CONCLUSIONS: The period of drug exposure in previously reported cases of patients with drug-induced interstitial pneumonia caused by dipeptidyl peptidase-4 inhibitor varied from several days to over 6 months. In the present case, our patient developed interstitial pneumonia only 1 day after the administration of vildagliptin. The precise mechanism of her vildagliptin-induced lung injury remains uncertain, but physicians should consider that dipeptidyl peptidase-4 inhibitor-induced lung injury, although rare, may appear acutely, even within days after administration of this drug. BioMed Central 2016-08-12 /pmc/articles/PMC4983085/ /pubmed/27520566 http://dx.doi.org/10.1186/s13256-016-1006-4 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Ohara, Nobumasa
Kaneko, Masanori
Sato, Kazuhiro
Maruyama, Ryoko
Furukawa, Tomoyasu
Tanaka, Junta
Kaneko, Kenzo
Kamoi, Kyuzi
Vildagliptin-induced acute lung injury: a case report
title Vildagliptin-induced acute lung injury: a case report
title_full Vildagliptin-induced acute lung injury: a case report
title_fullStr Vildagliptin-induced acute lung injury: a case report
title_full_unstemmed Vildagliptin-induced acute lung injury: a case report
title_short Vildagliptin-induced acute lung injury: a case report
title_sort vildagliptin-induced acute lung injury: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4983085/
https://www.ncbi.nlm.nih.gov/pubmed/27520566
http://dx.doi.org/10.1186/s13256-016-1006-4
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