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Good response to PAH-targeted drugs in a PVOD patient carrying Biallelic EIF2AK4 mutation

Pulmonary veno-occlusive disease (PVOD) is a rare and fatal cause of pulmonary arterial hypertension (PAH). Different from other types of PAH, PVOD patients have a dismal prognosis because of the progressive nature of pulmonary vascular involvement and fatal pulmonary edema induced by PAH-targeted d...

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Autores principales: Liang, Li, Su, Hua, Ma, Xiuqing, Zhang, Ruifeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167821/
https://www.ncbi.nlm.nih.gov/pubmed/30285736
http://dx.doi.org/10.1186/s12931-018-0900-2
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author Liang, Li
Su, Hua
Ma, Xiuqing
Zhang, Ruifeng
author_facet Liang, Li
Su, Hua
Ma, Xiuqing
Zhang, Ruifeng
author_sort Liang, Li
collection PubMed
description Pulmonary veno-occlusive disease (PVOD) is a rare and fatal cause of pulmonary arterial hypertension (PAH). Different from other types of PAH, PVOD patients have a dismal prognosis because of the progressive nature of pulmonary vascular involvement and fatal pulmonary edema induced by PAH-targeted drugs. Lung transplantation is the only choice for these patients. In a recent article published in the journal, Yang and his colleagues found pulmonary edema was not demonstrated in 2 of the 6 PVOD patients injected with prostacyclin analogues (a kind of PAH-targeted drug). Regretfully, none of these 6 patients underwent microscopic examination of lung tissues. Here, we reported a sporadic PVOD patient evidenced by pathology and EIF2AK4 biallelic mutation. The patient was followed over the course of 3 years in our center. During the 3 years, he was admitted into our hospital for many times for the acute exacerbation of pulmonary hypertension. However, after treatment with many kinds of PAH-targeted drugs, the pulmonary hypertension was in control and he feel better every time. The present patient displayed different treatment response comparing with previous reports. It suggests that PVOD is a heterogeneity population and different patients have different characteristics including clinical manifestation, genomics, treatment response et al. How to pick off this portion of patients timely is the core issue. Lots of important works are necessary to answer this question. However, we can see a glimmer of hope form this patient at least. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12931-018-0900-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-61678212018-10-09 Good response to PAH-targeted drugs in a PVOD patient carrying Biallelic EIF2AK4 mutation Liang, Li Su, Hua Ma, Xiuqing Zhang, Ruifeng Respir Res Letter to the Editor Pulmonary veno-occlusive disease (PVOD) is a rare and fatal cause of pulmonary arterial hypertension (PAH). Different from other types of PAH, PVOD patients have a dismal prognosis because of the progressive nature of pulmonary vascular involvement and fatal pulmonary edema induced by PAH-targeted drugs. Lung transplantation is the only choice for these patients. In a recent article published in the journal, Yang and his colleagues found pulmonary edema was not demonstrated in 2 of the 6 PVOD patients injected with prostacyclin analogues (a kind of PAH-targeted drug). Regretfully, none of these 6 patients underwent microscopic examination of lung tissues. Here, we reported a sporadic PVOD patient evidenced by pathology and EIF2AK4 biallelic mutation. The patient was followed over the course of 3 years in our center. During the 3 years, he was admitted into our hospital for many times for the acute exacerbation of pulmonary hypertension. However, after treatment with many kinds of PAH-targeted drugs, the pulmonary hypertension was in control and he feel better every time. The present patient displayed different treatment response comparing with previous reports. It suggests that PVOD is a heterogeneity population and different patients have different characteristics including clinical manifestation, genomics, treatment response et al. How to pick off this portion of patients timely is the core issue. Lots of important works are necessary to answer this question. However, we can see a glimmer of hope form this patient at least. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12931-018-0900-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-01 2018 /pmc/articles/PMC6167821/ /pubmed/30285736 http://dx.doi.org/10.1186/s12931-018-0900-2 Text en © The Author(s). 2018 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 Letter to the Editor
Liang, Li
Su, Hua
Ma, Xiuqing
Zhang, Ruifeng
Good response to PAH-targeted drugs in a PVOD patient carrying Biallelic EIF2AK4 mutation
title Good response to PAH-targeted drugs in a PVOD patient carrying Biallelic EIF2AK4 mutation
title_full Good response to PAH-targeted drugs in a PVOD patient carrying Biallelic EIF2AK4 mutation
title_fullStr Good response to PAH-targeted drugs in a PVOD patient carrying Biallelic EIF2AK4 mutation
title_full_unstemmed Good response to PAH-targeted drugs in a PVOD patient carrying Biallelic EIF2AK4 mutation
title_short Good response to PAH-targeted drugs in a PVOD patient carrying Biallelic EIF2AK4 mutation
title_sort good response to pah-targeted drugs in a pvod patient carrying biallelic eif2ak4 mutation
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167821/
https://www.ncbi.nlm.nih.gov/pubmed/30285736
http://dx.doi.org/10.1186/s12931-018-0900-2
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