Department of Dermatology, Mayo Clinic, Rochester, Minnesota.
Department of Pediatrics and Adolescent Medicine, Mayo Clinic, Rochester, Minnesota.
JAMA Dermatol. 2018 Mar 1;154(3):286-292. doi: 10.1001/jamadermatol.2017.5417.
Children with psoriasis are at increased risk for comorbidities. Many children with psoriasis are also overweight or obese; it is unknown whether the increased risk of comorbidities in these children is independent of obesity.
To determine the risk of elevated lipid levels (hyperlipidemia/hypertriglyceridemia), hypertension, metabolic syndrome, polycystic ovarian syndrome, diabetes, nonalcoholic liver disease, and elevated liver enzyme levels in children with and without psoriasis, after accounting for obesity.
DESIGN, SETTING, AND PARTICIPANTS: This was a retrospective cohort study of claims data from Optum Laboratories Data Warehouse (includes 150 million privately insured and Medicare enrollees). A cohort of 29 957 children with psoriasis (affected children) and an age-, sex-, and race-matched comparator cohort of 29 957 children without psoriasis were identified and divided into 4 groups: (1) nonobese, without psoriasis (reference cohort); (2) nonobese, with psoriasis; (3) obese, without psoriasis; and (4) obese, with psoriasis.
Risk of developing comorbidities (Cox proportional hazards regression).
The overall mean (SD) age of those included in the cohort was 12.0 (4.4) years, and 16 034 (53.5%) were girls. At baseline, more affected children were obese (862 [2.9%] vs 463 [1.5%]; P < .001 for all comparisons). Children with psoriasis were significantly more likely to develop each of the comorbidities than those without psoriasis (P < .01). Obesity was a strong risk factor for development of each comorbidity, even in those without psoriasis (hazard ratios [HRs] ranging from 2.26 to 18.11). The risk of comorbidities was 40% to 75% higher among nonobese children with vs without psoriasis: elevated lipid levels (HR, 1.42; 95% CI, 1.25-1.62), hypertension (HR, 1.64; 95% CI, 1.40-1.93), diabetes (HR, 1.58; 95% CI, 1.27-1.95), metabolic syndrome (HR, 1.62; 95% CI, 1.13-2.33), polycystic ovarian syndrome (HR, 1.49; 95% CI, 1.18-1.88), nonalcoholic liver disease (HR, 1.76; 95% CI, 1.16-2.65), and elevated liver enzyme levels (HR, 1.46; 95% CI, 1.27-1.67). Except for hypertension (P = .03), no significant interaction occurred between psoriasis and obesity on the risk of comorbidities.
Children with psoriasis are at greater risk of developing obesity, hyperlipidemia, hypertension, diabetes, metabolic syndrome, polycystic ovarian syndrome, nonalcoholic liver disease, and elevated liver function enzyme levels than children without psoriasis. While psoriasis is a small independent risk factor for the development of these comorbidities, obesity is a much stronger contributor to comorbidity development in children with psoriasis.
患有银屑病的儿童发生合并症的风险增加。许多患有银屑病的儿童也超重或肥胖;尚不清楚这些儿童合并症的风险是否独立于肥胖。
在考虑肥胖的情况下,确定患有和不患有银屑病的儿童中血脂水平升高(高脂血症/高甘油三酯血症)、高血压、代谢综合征、多囊卵巢综合征、糖尿病、非酒精性肝病和肝酶水平升高的风险。
设计、设置和参与者:这是一项来自 Optum 实验室数据仓库的索赔数据的回顾性队列研究(包括 1.5 亿名私人保险和医疗保险参保者)。确定了一个 29957 名患有银屑病的儿童队列(受影响的儿童)和一个年龄、性别和种族匹配的无银屑病的儿童对照组队列 29957 名,并将其分为 4 组:(1)非肥胖,无银屑病(参考队列);(2)非肥胖,有银屑病;(3)肥胖,无银屑病;和(4)肥胖,有银屑病。
发生合并症的风险(Cox 比例风险回归)。
队列中参与者的总体平均(SD)年龄为 12.0(4.4)岁,其中 16034 名(53.5%)为女孩。基线时,更多受影响的儿童肥胖(862[2.9%]比 463[1.5%];所有比较均 P < .001)。与无银屑病的儿童相比,患有银屑病的儿童更有可能患上每一种合并症(P < .01)。肥胖是发生每种合并症的强有力风险因素,即使在没有银屑病的儿童中也是如此(风险比 [HR] 范围为 2.26 至 18.11)。与无银屑病的非肥胖儿童相比,有银屑病的非肥胖儿童患合并症的风险高 40%至 75%:血脂水平升高(HR,1.42;95%CI,1.25-1.62)、高血压(HR,1.64;95%CI,1.40-1.93)、糖尿病(HR,1.58;95%CI,1.27-1.95)、代谢综合征(HR,1.62;95%CI,1.13-2.33)、多囊卵巢综合征(HR,1.49;95%CI,1.18-1.88)、非酒精性肝病(HR,1.76;95%CI,1.16-2.65)和肝酶水平升高(HR,1.46;95%CI,1.27-1.67)。除高血压(P = .03)外,银屑病和肥胖对合并症风险无显著交互作用。
患有银屑病的儿童发生肥胖、高脂血症、高血压、糖尿病、代谢综合征、多囊卵巢综合征、非酒精性肝病和肝功能酶水平升高的风险高于无银屑病的儿童。虽然银屑病是这些合并症发生的一个小的独立危险因素,但肥胖是导致患有银屑病的儿童发生合并症的一个更强的因素。