Pediatric psoriasis: Should we be concerned with comorbidity? Cross-sectional study

被引:14
作者
Kelati, Awatef [1 ]
Baybay, Hanane [1 ]
Najdi, Adil [2 ]
Zinoune, Safae [1 ]
Mernissi, Fatima Z. [1 ]
机构
[1] Univ Hosp Hassan II, Dept Dermatol, 202 Hay Mohamadi, Fes, Morocco
[2] Univ Med & Pharm Tangier, Dept Epidemiol & Publ Hlth, Tangier, Morocco
关键词
childhood; comorbidity; cross-sectional study; psoriasis; BODY-MASS INDEX; METABOLIC SYNDROME; CHILDHOOD PSORIASIS; CHILDREN; ASSOCIATION; EPIDEMIOLOGY; POPULATION; PREVALENCE; OVERWEIGHT; EPILEPSY;
D O I
10.1111/ped.13309
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BackgroundSimilarly to psoriasis in adults, recent research has linked psoriasis to several comorbidities in children. The aim of this study was therefore to describe comorbidities associated with pediatric psoriasis, to investigate their relationship with psoriasis characteristics and severity, and to perform a review of the literature. MethodsA cross-sectional study was performed on a sample of Moroccan children with psoriasis, in 2014-2016. ResultsA total of 64 pediatric psoriasis patients had metabolic comorbidities in association with psoriasis; 20 children had non-metabolic comorbidities; and 76 children had no comorbidity. The metabolic comorbidities were as follows: abdominal obesity, 40% (n = 64); overweight, 12.5% (n = 20); metabolic syndrome, 3.7% (n = 6); and dyslipidemia, 3.1% (n = 5); the non-metabolic comorbidities were atopy, 4.3% (n = 7); epilepsy, 3.1% (n = 5); celiac disease, 1.8% (n = 3); vitiligo, 1.8% (n = 3); alopecia ariata, 0.6% (n = 1); and valvular cardiopathy, 0.6% (n = 1). No cases of diabetes mellitus, obesity, or high blood pressure were recorded. Significant factors associated with metabolic comorbidity were extended psoriasis vulgaris >10% (P = 0.01; OR, 2.19), severe psoriasis especially pustular and erythroderma (P = 0.018; OR, 2), nail involvement (P = 0.016; OR, 1.5), face involvement (P = 0.01; OR, 1,59), resistance to topical treatment (P = 0.003; OR, 2.5) and alteration of quality of life (P = 0.02; OR, 1,7). There was no significant risk factor associated with non-metabolic comorbidity. ConclusionsGiven the frequent association of pediatric psoriasis with many disorders, these comorbidities should be investigated and identified so that they can be taken into account in the management of psoriasis in order to avoid treatment failure. Regular follow up should be carried out in patients at risk of metabolic comorbidity.
引用
收藏
页码:923 / 928
页数:6
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