Tồn Trữ Tài Liệu Khảo Cứu Y Dược Khoa Của Người Việt
Bs Anh-Tuan Dinh-Xuan và các đồng nghiệp với nghiên cứu:
Severe pulmonary hypertension: walking through new paths to revisit an old field

A.T. Dinh-Xuan1, M. Humbert2 and R. Naeije3
1 Service de Physiologie-Explorations Fonctionnelles, Centre Hospitalier Universitaire Cochin, Assistance Publique-Hôpitaux de Paris, Université Paris V, Paris, France, 2 Service de Pneumologie, Hôpital Antoine Béclère, Clamart, France, and 3 Dépt des Soins Intensifs, Hôpital Universitaire Erasme, Brussels, Belgium
CORRESPONDENCE: A.T. Dinh-Xuan, Service de Physiologie-Explorations Fonctionnelles, Hôpital Cochin, 27, rue du faubourg Saint-Jacques, 75679, Paris cedex 14, France. Fax: 33 158412345. E-mail: anh-tuan.dinh-xuan@cch.ap-hop-paris.fr

Almost 10 yrs ago, a series of manuscripts on pulmonary hypertension appeared in the European Respiratory Journal 1–9. These in-depth reviews caused a great deal of interest in the readers as they covered various aspects of this unique condition, which causes hypertension in a region of the body in which the artery blood pressure should always remain low, as opposed to its systemic counterpart. Almost 10 yrs later, exciting new stories about the origin, mechanisms, identification and cure of this pulmonary disorder have slowly emerged that are certainly worth telling now.
One of the most dramatic breakthroughs was the recent discovery of the role played by bone morphogenetic protein receptor type II (BMPR-II) gene in the pathophysiology of familial pulmonary hypertension 10. This led to a revival of interest in the use of genetic studies to dissect mechanisms and pathways leading to pulmonary vascular disease 12. However, it soon became clear that the discovery of genes involved in disease would be of little help if the signalling pathways that are perturbed as a result of gene mutation could not be delineated. Following the same pattern, another recent breakthrough, which will certainly shed new light on understanding of pulmonary vascular physiology, was the discovery that the serotonin transporter (5-HTT) could play a pivotal role in the mechanisms leading to pulmonary vascular remodelling and severe pulmonary hypertension 13. The crosstalk between 5-HTT and BMPR-II signalling pathways is yet to be clearly defined 14. Nevertheless, it is probable that these factors are not alone as other crucial players like gelatinase 15 or endothelin 16 are also likely to be involved in this complex and intricate biological puzzle.
Although understanding the cause of severe pulmonary hypertension is crucial, it is certainly not the ultimate target. The main concern remains how to detect the disease in its early development and how to cure patients of this dreadful condition. Fortunately, progress has been made on all fronts of this unique battle, ranging from noninvasive evaluation of pulmonary arterial pressure 17 to medical treatment and surgical procedures.
In this issue of the European Respiratory Journal, a new series of 12 reviews, written by those who are at the forefront of biological and clinical research in pulmonary hypertension, will begin with an article by Humbert and Trembath 18. The present authors hope that this series will be more than simply a sequel to the first series of manuscripts published 10 yrs ago, and are confident that these short reviews will provide insights and generate new ideas for readers when revisiting familiar fields of knowledge through recently discovered paths. Hopefully, this can be as interesting as rereading a favourite old book; re-examining the once overlooked pages and their obscure messages that become all at once obvious in the spotlight of new discoveries.

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