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Review

Mild asthma is not mild: risk factors and predictive biomarkers for severe acute exacerbations and progression in mild asthma

, , , & ORCID Icon
Pages 1261-1271 | Received 28 Oct 2023, Accepted 01 Feb 2024, Published online: 06 Feb 2024
 

ABSTRACT

Introduction

Asthma is a common chronic respiratory disease characterized by chronic airway inflammation, airway hyperresponsiveness, reversible airflow limitation, and airway remodeling. Mild asthma is the most common type of asthma, but it is the most neglected. Sometimes mild asthma can lead to acute severe exacerbations or even death.

Areas covered

This article reviews the epidemiology, risk factors, and possible predictors of acute severe exacerbations and disease progression in mild asthma to improve the understanding of mild asthma and its severe acute exacerbations and progression.

Expert opinion

There is a necessity to improve asthma patient categorization and redefine mild asthma’s concept to heighten patient and physician attention. Identifying mild asthma patients that are highly vulnerable to severe acute exacerbations and researching the mechanisms are future prioritizations.

Article highlights

  • Mild asthma may not be truly ‘mild,’ as this label could result in neglectful treatment and management of patients with mild asthma.

  • Some patients with mild asthma are at risk for poor control, acute exacerbations, reduced lung function and even death.

  • Multiple risk factors and biomarkers have the potential to recognize individuals with asthma who may have unfavorable outcomes.

  • Future research should focus on improved categorization of asthma, more effective management of emergency medication usage, and redefining the classification of ‘mild asthma.’

Abbreviations

ACQ=

Asthma control score

ALPL=

Alkaline phosphatase, liver/bone/kidney

AX=

Area of reactance

BAS=

Basophils

CPA3=

Carboxypeptidase A3

CTLA-4=

Cytotoxic T-lymphocyte-associated protein 4

CLC=

Charcot-Leyden crystal galectin

CMV=

Cytomegalovirus

CXCR2=

Chemokine (C‐X‐C motif) receptor 2

DNASEIL3=

Deoxyribonuclease I‐like3

EOS=

Eosinophils

FEV1=

Forced expiratory volume in the first second

FEF 25–75%=

Forced expiratory flow rate between 25% and 75%

GAWS=

Genome-wide association studies

HHV=

Human herpesvirus

H2S=

Hydrogen sulfide

ICS=

Inhaled corticosteroids

IL1B=

Interleukin 1 beta

IOS=

Impulse oscillometry

LBP=

Lipopolysaccharide binding protein

MBNW=

Multiple nitrogen washout

NEU=

Neutrophils

NFA=

Near-fatal asthma

PAL=

Persistent airflow limitation

PFTs=

Pulmonary function tests

R5=

The resistance at 5 Hz

R20=

The resistance at 20 Hz

RV=

Rhinovirus

SABA=

Short-acting beta-agonists

sCD=

Soluble cluster of differentiation

SNP=

Single nucleotide polymorphism

sST2=

Soluble growth stimulation expressed gene 2

TGFB1=

Transforming growth factor beta 1

X5=

Respiratory system impedance at 5 Hz

Declaration of interest

The authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.

Reviewer disclosures

A peer reviewer on this manuscript has received an honorarium from Expert Review of Respiratory Medicine for their review work. Peer reviewers on this manuscript have no other relevant financial relationships or otherwise to disclose.

Additional information

Funding

This work was supported by the National key Research and Development Program of China (No. 2021YFC2500702), the National Natural Science Foundation of China (No. 82270104), and the Health Commission of Hubei Province scientific research project (No. WJ2023Z010).