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Pediatric psoriasis: Should we be concerned with comorbidity? Cross-sectional study
Awatef Kelati1, Hanane Baybay1, Adil Najdi2
1Department of Dermatology, University Hospital Hassan II, Fez, Morocco.
Insights
Pediatric psoriasis is frequently linked to metabolic comorbidities like abdominal obesity and overweight. Early identification and management of these associated conditions are crucial for effective treatment and improved quality of life in children with psoriasis.
Area of Science:
- Pediatric Dermatology
- Metabolic Health
- Chronic Disease Comorbidity
Background:
- Recent research indicates a link between pediatric psoriasis and various comorbidities, similar to adult psoriasis.
- Understanding these associations is vital for comprehensive patient care.
- This study aims to describe comorbidities in children with psoriasis and their relationship to disease characteristics.
Purpose of the Study:
- To describe comorbidities associated with pediatric psoriasis.
- To investigate the relationship between comorbidities and psoriasis characteristics/severity.
- To conduct a literature review on pediatric psoriasis comorbidities.
Main Methods:
- A cross-sectional study was conducted.
- The study included Moroccan children diagnosed with psoriasis.
- Data was collected between 2014 and 2016.
Main Results:
- 64 children had metabolic comorbidities (abdominal obesity, overweight, metabolic syndrome, dyslipidemia).
- 7 children had non-metabolic comorbidities (atopy, epilepsy, celiac disease, vitiligo, alopecia ariata, valvular cardiopathy).
- Extended psoriasis vulgaris (>10% BSA), severe forms (pustular, erythroderma), nail/face involvement, resistance to treatment, and altered quality of life were significantly associated with metabolic comorbidity.
Conclusions:
- Pediatric psoriasis is frequently associated with numerous comorbidities.
- Investigating and identifying these comorbidities is essential for effective psoriasis management and preventing treatment failure.
- Regular follow-up is recommended for pediatric psoriasis patients at risk of metabolic comorbidity.
Background:
Similarly 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.
Methods:
A cross-sectional study was performed on a sample of Moroccan children with psoriasis, in 2014-2016.
Results:
A 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.
Conclusions:
Given 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.
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