Hidradenitis Suppurativa: Proposal of Classification in Two Endotypes with Two-Step Cluster Analysis

被引:26
作者
Gonzalez-Manso, Anxo [1 ]
Agut-Busquet, Eugenia [1 ,2 ]
Romani, Jorge [1 ,3 ]
Vilarrasa, Eva [1 ,2 ]
Bittencourt, Flavia [1 ,2 ]
Mensa, Anna [4 ]
Canto, Elisabeth [5 ]
Arostegui, Juan, I [4 ]
Vidal, Silvia [5 ]
机构
[1] Autonomous Univ Barcelona, Dept Med, Barcelona, Spain
[2] Hosp Santa Creu & Sant Pau, Dept Dermatol, Barcelona, Spain
[3] Consorci Sanitari Parc Tauli, Dept Dermatol, Parc Tauli 1, ES-08208 Sabadell, Spain
[4] Hosp Clin Barcelona, Dept Immunol, Barcelona, Spain
[5] Hosp Santa Creu & Sant Pau, Dept Immunol, Barcelona, Spain
关键词
Hidradenitis suppurativa; Endotypes; Phenotypes; PREVALENCE; PHENOTYPE; SKIN;
D O I
10.1159/000511045
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Introduction: Hidradenitis suppurativa (HS) is a chronic, inflammatory, recurrent disorder of the pilosebaceous unit. Currently, several attempts have been made to classify this disease according to its pathogenesis and clinical manifestations. We attempted at classifying 103 patients using two-step cluster analysis. Methods: The final model included body mass index, C-reactive protein (CRP), and serum concentrations of IL-1, IL-6, IL-17, and IL-10 as continuous variables, and sex, later/early onset, anterior/posterior lesion sites, presence/absence of sinus tracts, nodules and abscesses, positive/negative history of pilonidal sinus, and presence/absence of mutations in gamma-secretase subunits (APH1A, APH1B, MEFV, NCSTN, PSEN1, PSEN2, PSENEN, PSTPIP1) as qualitative variables. Results: The resultant model defined two groupings or clusters: cluster 1 (64.9% of patients) characterized by nonobese males, with nodular lesions in posterior sites, early-onset HS, higher IL-10, presence of gamma-secretase mutations, and history of pilonidal sinus; and cluster 2 (35.1% of patients) characterized by obese females or males, with lesions in anterior sites, more presence of sinus tracts and abscesses and less nodules, later-onset HS, and higher concentrations of IL-1, CRP, IL-17, and IL-6. Severity measures (Hurley, HS-PGA, and IHS4) and tobacco use were discarded because the analysis found them to be less relevant for clustering. Conclusion: Our resultant model confirms the clinical impression that HS is a disease spectrum with two pathogenic poles defining two clusters or endotypes. The probability of having severe disease was equally distributed in the two clusters. The variable with the highest predictive value for clustering was involvement of typical anterior sites (axillae, submammary) or atypical posterior sites (back, gluteal). Serum concentrations of interleukins, tobacco use, and sex had a lower predictive power for clustering.
引用
收藏
页码:365 / 371
页数:7
相关论文
共 34 条
[1]   Hidradenitis suppurativa of the nape: Description of an atypical phenotype related to severe early-onset disease in men [J].
Agut-Busquet, Eugenia ;
Romani, Jorge ;
Ribera, Miquel ;
Luelmo, Jesus .
JOURNAL OF DERMATOLOGY, 2019, 46 (02) :149-153
[2]   Genotype-phenotype correlation in inherited hidradenitis suppurativa: one step forward, one step back [J].
Alavi, A. ;
Piguet, V. .
BRITISH JOURNAL OF DERMATOLOGY, 2019, 181 (03) :443-444
[3]   Hidradenitis suppurativa: A comprehensive review [J].
Alikhan, Ali ;
Lynch, Peter J. ;
Eisen, Daniel B. .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2009, 60 (04) :539-561
[4]   Does obesity cause a distinct phenotype of hidradenitis suppurativa? [J].
Boer, J. .
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2018, 32 (05) :E195-E196
[5]   Identification of Three Hidradenitis Suppurativa Phenotypes: Latent Class Analysis of a Cross-Sectional Study [J].
Canoui-Poitrine, Florence ;
Le Thuaut, Aurelie ;
Revuz, Jean E. ;
Viallette, Cedric ;
Gabison, Germaine ;
Poli, Florence ;
Pouget, Florence ;
Wolkenstein, Pierre ;
Bastuji-Garin, Sylvie .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2013, 133 (06) :1506-1511
[6]   PAPA, PASH and PAPASH Syndromes: Pathophysiology, Presentation and Treatment [J].
Cugno, Massimo ;
Borghi, Alessandro ;
Marzano, Angelo V. .
AMERICAN JOURNAL OF CLINICAL DERMATOLOGY, 2017, 18 (04) :555-562
[7]   Preliminary findings suggesthidradenitis suppurativa may be due to defective follicular support [J].
Danby, F. W. ;
Jemec, G. B. E. ;
Marsch, W. Ch. ;
von Laffert, M. .
BRITISH JOURNAL OF DERMATOLOGY, 2013, 168 (05) :1034-1039
[8]   Gene expression of sphingolipid metabolism pathways is altered in hidradenitis suppurativa [J].
Dany, Mohammed ;
Elston, Dirk .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2017, 77 (02) :268-+
[9]   Hidradenitis suppurativa: a common and burdensome, yet under-recognised, inflammatory skin disease [J].
Dufour, Deirdre Nathalie ;
Emtestam, Lennart ;
Jemec, Gregor B. .
POSTGRADUATE MEDICAL JOURNAL, 2014, 90 (1062) :216-221
[10]   Inter-rater reliability of phenotypes and exploratory genotype-phenotype analysis in inherited hidradenitis suppurativa [J].
Frew, J. W. ;
Hawkes, J. E. ;
Sullivan-Whalen, M. ;
Gilleaudeau, P. ;
Krueger, J. G. .
BRITISH JOURNAL OF DERMATOLOGY, 2019, 181 (03) :566-571