Choi Young M, Famenini Shannon, Wu Jashin J
Resident Physician in Dermatology at the Los Angeles Medical Center in CA.
Physician at the University of California, Irvine.
Perm J. 2017;21:16-073. doi: 10.7812/TPP/16-073.
Inflammatory signaling may play an important role in the pathogenesis of pulmonary arterial hypertension (PAH).
To assess the incidence of PAH in patients with mild and severe psoriasis compared with their respective controls.
From January 2004 to November 2012, we performed a retrospective cohort study of patients with psoriasis in the Kaiser Permanente Southern California Health Plan. Patients with an International Classification of Diseases, Ninth Revision Clinical Modification diagnostic code for psoriasis (696.1) or psoriatic arthritis (696.0) without a prior diagnosis of primary PAH (416.0) or secondary PAH (416.8) were eligible for inclusion. Patients who had never received a diagnosis of psoriasis were frequency-matched by age, sex, and race to form the control cohorts.
Incidence of PAH in patients with psoriasis compared with matched controls.
There were 10,115 patients with mild psoriasis, 3821 with severe psoriasis, and 69,360 matched controls. On multivariable analysis, there was a significantly increased risk of PAH developing in the severe psoriasis cohort vs their controls (hazard ratio = 1.46, 95% confidence interval = 1.09-1.94).
The systemic inflammatory process underlying psoriasis may be a cause for an increased risk of PAH, but there are numerous secondary causes of PAH, some of which were not accounted for in our study. Further prospective, randomized controlled trials are necessary to establish psoriasis as a risk factor for PAH.
炎症信号通路可能在肺动脉高压(PAH)的发病机制中起重要作用。
评估轻度和重度银屑病患者与各自对照组相比PAH的发病率。
2004年1月至2012年11月,我们对南加州凯撒医疗集团永久健康计划中的银屑病患者进行了一项回顾性队列研究。符合纳入标准的患者需有国际疾病分类第九版临床修订版银屑病诊断代码(696.1)或银屑病关节炎诊断代码(696.0),且此前未诊断为原发性PAH(416.0)或继发性PAH(416.8)。从未被诊断为银屑病的患者按年龄、性别和种族进行频率匹配,以形成对照队列。
银屑病患者与匹配对照组中PAH的发病率。
有10115例轻度银屑病患者、3821例重度银屑病患者和69360例匹配对照组。多变量分析显示,与对照组相比,重度银屑病队列中发生PAH的风险显著增加(风险比=1.46,95%置信区间=1.09-1.94)。
银屑病潜在的全身炎症过程可能是PAH风险增加的一个原因,但PAH有许多继发原因,其中一些在我们的研究中未被考虑。需要进一步进行前瞻性随机对照试验,以确定银屑病是否为PAH的危险因素。