» Articles » PMID: 22095547

Severe Asthma: Lessons Learned from the National Heart, Lung, and Blood Institute Severe Asthma Research Program

Abstract

The National Heart, Lung, and Blood Institute Severe Asthma Research Program (SARP) has characterized over the past 10 years 1,644 patients with asthma, including 583 individuals with severe asthma. SARP collaboration has led to a rapid recruitment of subjects and efficient sharing of samples among participating sites to conduct independent mechanistic investigations of severe asthma. Enrolled SARP subjects underwent detailed clinical, physiologic, genomic, and radiological evaluations. In addition, SARP investigators developed safe procedures for bronchoscopy in participants with asthma, including those with severe disease. SARP studies revealed that severe asthma is a heterogeneous disease with varying molecular, biochemical, and cellular inflammatory features and unique structure-function abnormalities. Priorities for future studies include recruitment of a larger number of subjects with severe asthma, including children, to allow further characterization of anatomic, physiologic, biochemical, and genetic factors related to severe disease in a longitudinal assessment to identify factors that modulate the natural history of severe asthma and provide mechanistic rationale for management strategies.

Citing Articles

Patient-centred outcomes in severe asthma: fatigue, sleep, physical activity and work.

Ten Have L, Meulmeester F, de Jong K, Ten Brinke A Eur Respir Rev. 2025; 34(175).

PMID: 40044187 PMC: 11880904. DOI: 10.1183/16000617.0122-2024.


Integrative Roles of Pro-Inflammatory Cytokines on Airway Smooth Muscle Structure and Function in Asthma.

Ford M, Reza M, Ruwanpathirana A, Sathish V, Britt Jr R Immunol Rev. 2025; 330(1):e70007.

PMID: 39991781 PMC: 11848829. DOI: 10.1111/imr.70007.


A Multifaceted Exploration of Status Asthmaticus: A Retrospective Analysis in a Romanian Hospital.

Trusculescu A, Ancusa V, Pescaru C, Wellmann N, Fira-Mladinescu C, Oancea C J Clin Med. 2024; 13(21).

PMID: 39518753 PMC: 11546779. DOI: 10.3390/jcm13216615.


Ciliary Function, Antigen Stasis and Asthma.

Marozkina N Int J Mol Sci. 2024; 25(18).

PMID: 39337527 PMC: 11432119. DOI: 10.3390/ijms251810043.


Respiratory symptoms, exacerbations and sleep disturbances are more common among participants with asthma and chronic airflow limitation: an epidemiological study in Estonia, Iceland and Sweden.

Mindus S, Gislason T, Benediktsdottir B, Jogi R, Moverare R, Malinovschi A BMJ Open Respir Res. 2024; 11(1).

PMID: 38373820 PMC: 10882325. DOI: 10.1136/bmjresp-2023-002063.


References
1.
Moore W, Bleecker E, Curran-Everett D, Erzurum S, Ameredes B, Bacharier L . Characterization of the severe asthma phenotype by the National Heart, Lung, and Blood Institute's Severe Asthma Research Program. J Allergy Clin Immunol. 2007; 119(2):405-13. PMC: 2837934. DOI: 10.1016/j.jaci.2006.11.639. View

2.
Wedes S, Khatri S, Zhang R, Wu W, Comhair S, Wenzel S . Noninvasive markers of airway inflammation in asthma. Clin Transl Sci. 2010; 2(2):112-7. PMC: 2838203. DOI: 10.1111/j.1752-8062.2009.00095.x. View

3.
Jarjour N, Peters S, Djukanovic R, Calhoun W . Investigative use of bronchoscopy in asthma. Am J Respir Crit Care Med. 1998; 157(3 Pt 1):692-7. DOI: 10.1164/ajrccm.157.3.9705020. View

4.
Busacker A, Newell Jr J, Keefe T, Hoffman E, Granroth J, Castro M . A multivariate analysis of risk factors for the air-trapping asthmatic phenotype as measured by quantitative CT analysis. Chest. 2008; 135(1):48-56. PMC: 2849984. DOI: 10.1378/chest.08-0049. View

5.
Levy B, Bonnans C, Silverman E, Palmer L, Marigowda G, Israel E . Diminished lipoxin biosynthesis in severe asthma. Am J Respir Crit Care Med. 2005; 172(7):824-30. PMC: 2718403. DOI: 10.1164/rccm.200410-1413OC. View