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Related Concept Videos

Asthma-II: Pathophysiology and Classification01:26

Asthma-II: Pathophysiology and Classification

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Asthma is a prevalent chronic respiratory condition marked by inflammation and hyperresponsiveness of the airways. Its pathophysiology involves complex interactions among inflammatory pathways, immune responses, and neural mechanisms.
Additionally, environmental and genetic factors play crucial roles in determining an individual's susceptibility to asthma and the severity of their condition.
Critical processes in asthma pathophysiology include:
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Asthma: Pathogenesis and Management01:20

Asthma: Pathogenesis and Management

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Asthma is a chronic pulmonary condition involving inflammation of the airways, hyper-reactivity, and reversible obstruction of the airways. This condition can significantly impact a person's quality of life, making breathing difficult and leading to distressing symptoms.
Asthma is classified as allergic and non-allergic. Allergens such as dust mites, pollen, and pet dander trigger allergic asthma, while factors like cold air, intense emotions, or exercise can induce non-allergic asthma.
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Antiasthma Drugs: Leukotriene Modifiers01:19

Antiasthma Drugs: Leukotriene Modifiers

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Leukotriene modifiers, or cysteinyl leukotriene receptor antagonists, are medications used to manage chronic asthma. These agents target specific inflammatory mediators produced during arachidonic acid metabolism, an essential process in generating inflammation in the body.
Leukotriene modifiers work through two distinct mechanisms:
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Asthma-IV: Diagnostic and Management01:30

Asthma-IV: Diagnostic and Management

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The diagnosis and management of asthma are comprehensive, encompassing clinical assessments, lung function tests, and pharmacological interventions. Here's an overview:
Clinical Assessment for Asthma:
This is the first step in diagnosing and managing asthma. It includes:
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Antiasthma Drugs: Mast Cell Stabilizers and Anti-IgE Drugs01:25

Antiasthma Drugs: Mast Cell Stabilizers and Anti-IgE Drugs

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Asthma is a chronic respiratory condition for which new therapeutic avenues, including anti-inflammatory drugs like mast cell stabilizers and anti-IgE treatments, continue to be developed.
Mast cell stabilizers, such as cromolyn (also known as sodium cromoglycate) and nedocromil (Tilade), are effective drugs in asthma management. These stabilizers hinder histamine release by skillfully obstructing the activation of mast cells and other cellular entities. Notably, they navigate this task without...
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Antiasthma Drugs: β2-Adrenoceptor Agonists01:25

Antiasthma Drugs: β2-Adrenoceptor Agonists

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Bronchodilators are critical in managing asthma, a chronic respiratory condition characterized by airway constriction due to inflammation and hyper-reactivity. Specifically, bronchodilators ease this constriction by relaxing the bronchial muscles, facilitating easier breathing.
One class of bronchodilators includes β2-adrenoceptor agonists. These agents target the β2-adrenoceptors located on bronchial smooth muscle cells. By stimulating these receptors, β2-agonists induce...
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Related Experiment Video

Updated: Mar 7, 2026

Dry Powder and Nebulized Aerosol Inhalation of Pharmaceuticals Delivered to Mice Using a Nose-only Exposure System
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Phenotype-Driven Therapeutics in Severe Asthma.

Maria Theresa D Opina1, Wendy C Moore2

  • 1Department of Pulmonary, Critical Care, Allergy, and Immunologic Diseases, Wake Forest School of Medicine, Medical Center Blvd, Winston-Salem, NC, 27157, USA.

Current Allergy and Asthma Reports
|February 25, 2017
PubMed
Summary
This summary is machine-generated.

Severe asthma treatment is complex due to patient heterogeneity. This review explores severe asthma phenotypes and novel treatments to personalize care for better symptom control and fewer exacerbations.

Keywords:
Asthma exacerbationsBiologicsBiomarkersPersonalized medicinePhenotypesSevere asthma

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Area of Science:

  • Pulmonology
  • Allergy and Immunology
  • Clinical Medicine

Background:

  • Inhaled corticosteroids (ICS) and long-acting β-agonists (LABA) are standard severe asthma treatments.
  • Some patients remain refractory to high-dose ICS/LABA therapy.
  • Severe asthma exhibits significant heterogeneity, with distinct phenotypes influencing treatment response.

Purpose of the Study:

  • To review severe asthma phenotypes identified through unbiased clustering.
  • To discuss recent evidence on novel targeted therapies for severe asthma.
  • To guide personalized treatment strategies for severe asthma.

Main Methods:

  • Literature review of severe asthma phenotypes.
  • Analysis of recent randomized controlled trials (RCTs) on add-on therapies.
  • Discussion of unbiased clustering approaches for phenotype identification.

Main Results:

  • Severe asthma is heterogeneous with identifiable phenotypes.
  • Personalized treatment approaches targeting specific phenotypes show promise.
  • Novel add-on therapies are emerging for refractory severe asthma.

Conclusions:

  • A "one size fits all" approach is inadequate for severe asthma.
  • Understanding severe asthma phenotypes is crucial for effective treatment.
  • Personalizing therapy based on phenotype and emerging treatments improves outcomes.