Comparison of hypothesis- and data-driven asthma phenotypes in NHANES 2007-2012: the importance of comprehensive data availability.

Asthma Phenotypes Population-based study Unsupervised analysis

Journal

Clinical and translational allergy
ISSN: 2045-7022
Titre abrégé: Clin Transl Allergy
Pays: England
ID NLM: 101576043

Informations de publication

Date de publication:
2019
Historique:
received: 04 01 2019
accepted: 01 03 2019
entrez: 29 3 2019
pubmed: 29 3 2019
medline: 29 3 2019
Statut: epublish

Résumé

Half of the adults with current asthma among the US National Health and Nutrition Examination Survey (NHANES) participants could be classified in more than one hypothesis-driven phenotype. A data-driven approach applied to the same subjects may allow a more useful classification compared to the hypothesis-driven one. To compare previously defined hypothesis-driven with newly derived data-driven asthma phenotypes, identified by latent class analysis (LCA), in adults with current asthma from NHANES 2007-2012. Adults (≥ 18 years) with current asthma from the NHANES were included (n = 1059). LCA included variables commonly used to subdivide asthma. LCA models were derived independently according to age groups: < 40 and ≥ 40 years old. Two data-driven phenotypes were identified among adults with current asthma, for both age groups. The proportions of the hypothesis-driven phenotypes were similar among the two data-driven phenotypes (p > 0.05). Class A < 40 years ( Both data- and hypothesis-driven approaches using clinical and physiological variables commonly used to characterize asthma are suboptimal to identify asthma phenotypes among adults from the general population. Further studies based on more comprehensive disease features are required to identify asthma phenotypes in population-based studies.

Sections du résumé

BACKGROUND BACKGROUND
Half of the adults with current asthma among the US National Health and Nutrition Examination Survey (NHANES) participants could be classified in more than one hypothesis-driven phenotype. A data-driven approach applied to the same subjects may allow a more useful classification compared to the hypothesis-driven one.
AIM OBJECTIVE
To compare previously defined hypothesis-driven with newly derived data-driven asthma phenotypes, identified by latent class analysis (LCA), in adults with current asthma from NHANES 2007-2012.
METHODS METHODS
Adults (≥ 18 years) with current asthma from the NHANES were included (n = 1059). LCA included variables commonly used to subdivide asthma. LCA models were derived independently according to age groups: < 40 and ≥ 40 years old.
RESULTS RESULTS
Two data-driven phenotypes were identified among adults with current asthma, for both age groups. The proportions of the hypothesis-driven phenotypes were similar among the two data-driven phenotypes (p > 0.05). Class A < 40 years (
CONCLUSION CONCLUSIONS
Both data- and hypothesis-driven approaches using clinical and physiological variables commonly used to characterize asthma are suboptimal to identify asthma phenotypes among adults from the general population. Further studies based on more comprehensive disease features are required to identify asthma phenotypes in population-based studies.

Identifiants

pubmed: 30918624
doi: 10.1186/s13601-019-0258-7
pii: 258
pmc: PMC6419396
doi:

Types de publication

Journal Article

Langues

eng

Pagination

17

Déclaration de conflit d'intérêts

The authors declare that they have no competing interests.

Références

Am J Respir Crit Care Med. 2005 Apr 15;171(8):912-30
pubmed: 15817806
Eur Respir J. 2005 Aug;26(2):319-38
pubmed: 16055882
Lancet. 2006 Aug 26;368(9537):804-13
pubmed: 16935691
Am J Respir Crit Care Med. 2008 Feb 1;177(3):253-60
pubmed: 18006882
Am J Respir Crit Care Med. 2008 Aug 1;178(3):218-224
pubmed: 18480428
Thorax. 2008 Nov;63(11):974-80
pubmed: 18678704
Lancet. 2008 Sep 20;372(9643):1017-9
pubmed: 18805315
Chest. 2010 Jan;137(1):138-45
pubmed: 19741060
Am J Respir Crit Care Med. 2010 Feb 15;181(4):315-23
pubmed: 19892860
Eur Respir J. 2011 Aug;38(2):310-7
pubmed: 21233270
Genome Med. 2011 Jul 06;3(7):43
pubmed: 21745417
J Allergy Clin Immunol. 2012 Aug;130(2):397-402.e2
pubmed: 22633327
Eur Respir J. 2012 Dec;40(6):1324-43
pubmed: 22743675
Pediatr Pulmonol. 2013 Jul;48(7):683-92
pubmed: 23401430
Allergy. 2013;68(5):674-80
pubmed: 23590217
Am J Respir Crit Care Med. 2013 Dec 1;188(11):1303-12
pubmed: 24180417
Am J Respir Crit Care Med. 2014 Jan 15;189(2):129-38
pubmed: 24283801
J Allergy Clin Immunol. 2014 May;133(5):1280-8
pubmed: 24589344
Clin Transl Allergy. 2014 Aug 04;4:24
pubmed: 25136441
Chron Respir Dis. 2015 Feb;12(1):47-60
pubmed: 25540134
Respir Med. 2016 Jan;110:1-11
pubmed: 26525374
J Allergy Clin Immunol. 2017 Jun;139(6):1797-1807
pubmed: 27773852
Data Brief. 2016 Nov 09;9:926-930
pubmed: 27896298
Respir Res. 2017 Jan 23;18(1):24
pubmed: 28114991
J Allergy Clin Immunol. 2017 Feb;139(2):388-399
pubmed: 28183433
Allergy. 2017 Nov;72(11):1753-1760
pubmed: 28398635
Lancet. 2018 Jan 27;391(10118):350-400
pubmed: 28911920
J Allergy Clin Immunol Pract. 2018 May - Jun;6(3):955-961.e1
pubmed: 29133218
Allergy. 2018 Aug;73(8):1622-1631
pubmed: 29569295
Clin Transl Allergy. 2018 May 4;8:13
pubmed: 29755730
Allergy. 2018 Oct;73(10):1964-1978
pubmed: 29869791
Ann Allergy Asthma Immunol. 2018 Oct;121(4):414-420
pubmed: 30059792
J Appl Physiol (1985). 2018 Nov 1;125(5):1620-1626
pubmed: 30161011
J Allergy Clin Immunol Pract. 2019 Feb;7(2):556-567.e15
pubmed: 30170162
Allergy. 2019 Apr;74(4):698-708
pubmed: 30447164
Am J Respir Crit Care Med. 1999 Jan;159(1):179-87
pubmed: 9872837

Auteurs

Rita Amaral (R)

1CINTESIS - Center for Health Technology and Services Research, Faculty of Medicine, University of Porto, Edifício Nascente, Piso 2, Rua Dr. Plácido da Costa, s/n, 4200-450 Porto, Portugal.
Department of Cardiovascular and Respiratory Sciences, Porto Health School, Porto, Portugal.

Ana M Pereira (AM)

1CINTESIS - Center for Health Technology and Services Research, Faculty of Medicine, University of Porto, Edifício Nascente, Piso 2, Rua Dr. Plácido da Costa, s/n, 4200-450 Porto, Portugal.
Department of Allergy, Instituto & Hospital CUF, Porto, Portugal.

Tiago Jacinto (T)

1CINTESIS - Center for Health Technology and Services Research, Faculty of Medicine, University of Porto, Edifício Nascente, Piso 2, Rua Dr. Plácido da Costa, s/n, 4200-450 Porto, Portugal.
Department of Cardiovascular and Respiratory Sciences, Porto Health School, Porto, Portugal.

Andrei Malinovschi (A)

4Department of Medical Sciences, Clinical Physiology, Uppsala University, Uppsala, Sweden.

Christer Janson (C)

5Department of Medical Sciences, Respiratory Medicine and Allergology, Uppsala University, Uppsala, Sweden.

Kjell Alving (K)

6Department of Women's and Children's Health, Paediatric Research, Uppsala University, Uppsala, Sweden.

João A Fonseca (JA)

1CINTESIS - Center for Health Technology and Services Research, Faculty of Medicine, University of Porto, Edifício Nascente, Piso 2, Rua Dr. Plácido da Costa, s/n, 4200-450 Porto, Portugal.
Department of Allergy, Instituto & Hospital CUF, Porto, Portugal.
7MEDCIDS - Department of Community Medicine, Information, and Health Sciences, Faculty of Medicine, University of Porto, Porto, Portugal.

Classifications MeSH