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Kidney disease in moderate‐to‐severe psoriasis: a critical appraisal
Author(s) -
JabbarLopez Z.K.,
Weatherhead S.C.,
Reynolds N.J.
Publication year - 2016
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/bjd.14302
Subject(s) - psoriasis , medicine , medical prescription , cohort , kidney disease , diagnosis code , population , medical record , cohort study , body surface area , renal function , dermatology , environmental health , pharmacology
Summary Aim Using a population‐based cohort, Wan et al . examined the risk of moderate‐to‐advanced (stage 3–5) chronic kidney disease ( CKD ) in patients with psoriasis. Setting and design A population‐based cohort was constructed using The Health Improvement Network ( THIN ) database. THIN is an electronic primary healthcare records database containing routinely collected medical diagnosis and drug prescribing data on > 9 million patients in the U.K. Data were collected prospectively on 143 883 adults (aged 18–90 years) with psoriasis. Of these, 7354 had severe psoriasis, as defined by prescription codes for systemic medication or treatment codes for phototherapy. Patients with psoriasis were matched with up to five nonpsoriasis age‐ and practice‐matched controls. Patients with a diagnosis of CKD before study entry were excluded. In addition, baseline data from the Incident Health Outcomes and Psoriasis Events ( iHOPE ) study, a cohort of 8731 primary care patients aged 25–64 years with psoriasis, was included. Psoriasis severity was categorized according to body surface area ( BSA ) involvement as estimated by general practitioners. A similar method using a patient‐reported BSA assessment tool was previously validated by the same group. Patients were matched by age and practice with 10 nonpsoriasis controls. Study exposure Psoriasis, identified on the basis of a recorded diagnostic code for psoriasis. Outcomes Incident CKD was defined as the presence of a recorded diagnostic code consistent with moderate‐to‐advanced (stage 3–5) CKD or laboratory parameters consistent with the diagnosis (estimated glomerular filtration rate < 60 mL min −1 1·73 m −2 ) during follow‐up. Prevalent CKD (as defined above) in the cross‐sectional data from the iHOPE study. Results The adjusted hazard ratios for incident CKD were 1·05 [95% confidence interval ( CI ) 1·02–1·07], 0·99 (95% CI 0·97–1·02) and 1·93 (95% CI 1·79–2·08) in the overall, mild and severe psoriasis groups, respectively. In the nested cross‐sectional study ( iHOPE ) the adjusted prevalence odds ratios for CKD were 0·89 (95% CI 0·72–1·10), 1·36 (95% CI 1·06–1·74) and 1·58 (95% CI 1·07–2·34) in the mild, moderate and severe psoriasis groups, respectively. Conclusions Moderate‐to‐severe psoriasis is associated with an increased risk of moderate‐to‐advanced CKD , independently of traditional risk factors.