Literature DB >> 26290279

New pharmacotherapy options for pulmonary arterial hypertension.

Swanny Perrin1,2, Marie-Camille Chaumais1,2,3, Caroline O'Connell2,4,5, David Amar2,4,5, Laurent Savale2,4,5, Xavier Jaïs2,4,5, David Montani2,4,5, Marc Humbert2,4,5, Gérald Simonneau2,4,5, Olivier Sitbon2,4,5.   

Abstract

INTRODUCTION: Epoprostenol was the first targeted therapy available for the treatment of pulmonary arterial hypertension (PAH). Since then great advances in our knowledge of the disease have been made and the spectrum of therapeutic options for PAH has expanded. After an overview of current available treatments, this article describes the new pharmacotherapy options and their place in the management of PAH. AREAS COVERED: This paper is based on a literature search and the review of studies published on PAH pharmacotherapy using the MEDLINE database. EXPERT OPINION: The last decade has been particularly important in PAH management with the emergence of six new molecules, the development of novel routes of administration and improvement of pharmacokinetics. Moreover, pediatric formulations have been developed. However, further research is required to inform clinicians regarding optimal choices of combination therapies (progressive add-on therapy or upfront combination therapy, selection of associated molecules regarding the patient's profile...), to continue to improve the quality of life of patients with new drugs and to reach the ultimate goal of curing the disease.

Entities:  

Keywords:  endothelin pathway; nitric oxide pathway; prostacyclin pathway; pulmonary arterial hypertension; updated treatment recommendations

Mesh:

Substances:

Year:  2015        PMID: 26290279     DOI: 10.1517/14656566.2015.1074177

Source DB:  PubMed          Journal:  Expert Opin Pharmacother        ISSN: 1465-6566            Impact factor:   3.889


  8 in total

1.  Iloprost attenuates hyperoxia-mediated impairment of lung development in newborn mice.

Authors:  Nelida Olave; Charitharth Vivek Lal; Brian Halloran; Vineet Bhandari; Namasivayam Ambalavanan
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2018-06-28       Impact factor: 5.464

Review 2.  Origin and production of inflammatory perivascular macrophages in pulmonary hypertension.

Authors:  Jonathan Florentin; Partha Dutta
Journal:  Cytokine       Date:  2017-08-30       Impact factor: 3.861

Review 3.  Discerning functional hierarchies of microRNAs in pulmonary hypertension.

Authors:  Vinny Negi; Stephen Y Chan
Journal:  JCI Insight       Date:  2017-03-09

4.  Inflammatory Macrophage Expansion in Pulmonary Hypertension Depends upon Mobilization of Blood-Borne Monocytes.

Authors:  Jonathan Florentin; Emilie Coppin; Sathish Babu Vasamsetti; Jingsi Zhao; Yi-Yin Tai; Ying Tang; Yingze Zhang; Annie Watson; John Sembrat; Mauricio Rojas; Sara O Vargas; Stephen Y Chan; Partha Dutta
Journal:  J Immunol       Date:  2018-04-09       Impact factor: 5.422

Review 5.  BMP type II receptor as a therapeutic target in pulmonary arterial hypertension.

Authors:  Mar Orriols; Maria Catalina Gomez-Puerto; Peter Ten Dijke
Journal:  Cell Mol Life Sci       Date:  2017-04-26       Impact factor: 9.261

6.  Role of miR-223-3p in pulmonary arterial hypertension via targeting ITGB3 in the ECM pathway.

Authors:  Aijun Liu; Yifan Liu; Bin Li; Ming Yang; Yang Liu; Junwu Su
Journal:  Cell Prolif       Date:  2018-12-03       Impact factor: 6.831

7.  Global Proteomics Deciphered Novel-Function of Osthole Against Pulmonary Arterial Hypertension.

Authors:  Li Yao; Yuxia Yang; Guanhong He; Chunqing Ou; Lan Wang; Kaixuan Liu
Journal:  Sci Rep       Date:  2018-04-03       Impact factor: 4.379

8.  Conditioned medium from M2b macrophages modulates the proliferation, migration, and apoptosis of pulmonary artery smooth muscle cells by deregulating the PI3K/Akt/FoxO3a pathway.

Authors:  Suiqing Huang; Yuan Yue; Kangni Feng; Xiaolin Huang; Huayang Li; Jian Hou; Song Yang; Shaojie Huang; Mengya Liang; Guangxian Chen; Zhongkai Wu
Journal:  PeerJ       Date:  2020-05-05       Impact factor: 2.984

  8 in total

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