Ampath Chats

Making Sense of the Laboratory Diagnosis of Asthma

Ampath Chats
Making Sense of the Laboratory Diagnosis of Asthma
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PATHCHAT Edition No. 89
Published: May 2024
Please contact your local Ampath pathologist for more information.

Authors:

  • Dr. Sylvia van den Berg
  • Dr. Carla van Heerden

Key Messages

Laboratory Evaluation of Asthma Includes:

  • Routine laboratory tests and Type 2 (T2) inflammation biomarkers.
  • Full blood count (FBC) with differential count: Helps confirm or exclude eosinophilia.
  • Sputum eosinophils: Persistently high levels despite high-dose corticosteroids are linked to more severe disease.
  • Total serum IgE: Determines eligibility for anti-IgE therapy.
  • Specific IgE: Identifies triggering allergens.
  • Fractional exhaled nitric oxide (FeNO): A non-invasive test used for diagnosis and monitoring.

📌 Asthma classification based on biomarkers enables precision treatment.

Introduction to Asthma

Asthma as a Global Health Concern

  • Affects over 260 million people worldwide.
  • Causes more than 450,000 deaths annually, most of which are preventable.
  • Most common chronic disease in children.

Pathophysiology of Asthma

  • Characterized by chronic airway inflammation, hyper-responsiveness, and variable airflow limitation.
  • Triggered by viruses, allergens, irritants, and exercise.
  • Symptoms include:
    • Wheezing.
    • Shortness of breath.
    • Chest tightness.
    • Coughing.
  • Episodes are reversible with bronchodilators or corticosteroids.

Personalized Treatment Approach

  • Asthma is now recognized as a heterogeneous disease with different molecular mechanisms.
  • Classifying asthma based on endotypes enables a targeted approach to treatment.

📌 Asthma treatment is shifting from a "one-size-fits-all" approach to precision medicine based on biomarkers.

What is Severe Asthma?

Definition of Severe Asthma

  • Affects 5–10% of asthmatics.
  • Requires high-dose inhaled corticosteroids (ICS) plus a second controller (e.g., LABA or systemic corticosteroids).
  • Remains uncontrolled despite optimal therapy.
  • Exacerbating factors must be corrected before diagnosing severe asthma.

📌 Severe asthma requires intensive monitoring and specialized treatment, including biologic therapies.

Endotypes and Phenotypes of Asthma

Asthma Classification Based on Molecular Pathways

  • Asthma was previously classified by phenotype (observable clinical traits).
  • Now categorized into endotypes based on underlying molecular mechanisms.

1. T2-High Asthma

  • Most common form of asthma.
  • Involves Th2 lymphocytes, IL-4, IL-5, and IL-13 cytokines.
  • Driven by eosinophilic inflammation.

Atopic Asthma

  • Early onset, well-defined, steroid-sensitive.
  • Associated with allergic sensitization.
  • Key biomarkers:
    • Elevated eosinophils (blood/sputum).
    • High FeNO.
    • Elevated total and specific IgE.

Late-Onset Eosinophilic Asthma

  • Adult-onset, often severe, associated with nasal polyps.
  • Key biomarkers:
    • Elevated eosinophils and FeNO.

Aspirin-Exacerbated Respiratory Disease (AERD)

  • Adult-onset, triggered by NSAIDs.
  • Key biomarker:
    • Urinary leukotriene E4 (LTE4).

2. Non-T2 (T2-Low) Asthma

  • Less understood, may involve Th1/Th17 inflammation.
  • Poor response to inhaled corticosteroids.

Neutrophilic Asthma

  • Adult-onset, associated with smoking and obesity.
  • Key biomarker:
    • Induced sputum neutrophil count >50%.

📌 Identifying the asthma endotype is crucial for selecting the most effective treatment strategy.

Biomarkers of Asthma

Blood and Sputum Eosinophils

  • Strongly associated with Type 2 inflammation.
  • Eosinophil count >0.3 × 10⁹/L predicts exacerbation risk.
  • Sputum eosinophils >2% indicate airway inflammation.

Fractional Exhaled Nitric Oxide (FeNO)

  • Non-invasive marker of airway inflammation.
  • Higher in T2-high asthma.
  • Diagnostic cut-offs:
    • <25 ppb (adults) or <20 ppb (children) → Low likelihood of T2 asthma.
    • ≥50 ppb (adults) or ≥35 ppb (children) → Suggests eosinophilic inflammation.

Total and Specific IgE

  • High total IgE correlates with asthma severity.
  • Specific IgE identifies allergen triggers.

📌 Using multiple biomarkers improves diagnostic accuracy and guides personalized treatment.

Using Biomarkers to Guide Asthma Management

Stepwise Approach to Asthma Treatment Based on Biomarkers

Step 1: Determine T2 Status

  • T2-high asthma is defined by:
    • High FeNO.
    • Elevated blood eosinophils.
    • Allergic sensitization (specific IgE or skin prick test).

Step 2: Select Appropriate Treatment

  • T2-high asthma:
    • ICS therapy.
    • Biologics (omalizumab, dupilumab, mepolizumab) if severe.
  • T2-low asthma:
    • Consider alternative treatments (e.g., macrolides, bronchodilators).

📌 Personalized asthma treatment improves symptom control and reduces exacerbations.

Asthma Monitoring with FeNO Testing

FeNO Testing Now Available at Selected Ampath Facilities

  • Easy, non-invasive point-of-care test.
  • Monitors airway inflammation and corticosteroid response.
  • Factors that affect FeNO results:
    • Age, gender, smoking, food intake, infections, allergic rhinitis, asthma medications.

📌 FeNO testing provides a convenient tool for diagnosing and managing asthma in clinical practice.

Key Takeaways for Clinicians

Asthma diagnosis and management should be guided by biomarkers.
T2-high asthma responds well to corticosteroids and biologics, while T2-low asthma requires alternative approaches.
Blood eosinophils, FeNO, and IgE testing help classify asthma endotypes.
FeNO testing is a valuable non-invasive tool for monitoring airway inflammation.
Personalized treatment improves patient outcomes and reduces asthma-related hospitalizations.

📌 Precision medicine is transforming asthma care by allowing targeted therapy based on molecular mechanisms.