Chronic kidney disease in patients with psoriatic arthritis: a cohort study

被引:0
|
作者
Kharouf, Fadi [1 ,2 ]
Gao, Shangyi [1 ]
Al-Matar, Shahad [1 ,2 ]
Cook, Richard J. [3 ]
Chandran, Vinod [1 ,2 ,4 ,5 ]
Gladman, Dafna D. [1 ,2 ,5 ]
机构
[1] Univ Hlth Network, Schroeder Arthrit Inst, Krembil Res Inst, Ctr Prognosis Studies Rheumat Dis,Krembil Gladman, Toronto, ON, Canada
[2] Univ Toronto, Dept Med, Div Rheumatol, Toronto, ON, Canada
[3] Univ Waterloo, Dept Stat & Actuarial Sci, Waterloo, ON, Canada
[4] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[5] Univ Toronto, Inst Med Sci, Toronto, ON, Canada
来源
RMD OPEN | 2024年 / 10卷 / 04期
关键词
Psoriatic Arthritis; Methotrexate; Anti-Inflammatory Agents; Non-Steroidal; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; STAGE RENAL-DISEASE; CLINICAL-TRIALS; POPULATION; METHOTREXATE; RISK; CKD; CLASSIFICATION; COMORBIDITY; NSAIDS;
D O I
10.1136/rmdopen-2024-004636
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives Chronic kidney disease (CKD) is a comorbidity in psoriatic arthritis (PsA). We aimed to define the prevalence of CKD in patients with PsA, describe their long-term renal outcomes and identify risk factors for CKD development. Methods We included patients with PsA followed by our prospective observational cohort. We defined CKD as an estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m(2) for at least 3 months. We characterised long-term renal outcomes of CKD cases identified following clinic entry. We used time-dependent Cox regression models to identify factors associated with CKD development. Results Of 1336 patients included in the study, 123 (9.2%) had CKD. Of these, 25 (20.3%) were observed to have CKD at clinic entry and 98 (79.7%) developed CKD during follow-up at a median (IQR) of 8.2 (2.8-14.0) years from baseline. Doubling of baseline creatinine was observed in 18 of 98 (18.3%) new patients with CKD. 49 (50%) patients developed a sustained >= 40% reduction in baseline eGFR. Two patients developed eGFR <15 mL/min/1.73 m(2). In the multivariate Cox regression model adjusted for age at study entry, sex and baseline eGFR, factors independently associated with the development of CKD included diabetes mellitus (HR 2.58, p<0.001), kidney stones (HR 2.14, p=0.01), radiographic damaged joint count (HR 1.02, p=0.02), uric acid (HR 1.21, p<0.001; 50-unit increase), daily use of non-steroidal anti-inflammatory drugs (NSAIDs) (HR 1.77, p=0.02) and methotrexate use (HR 0.51, p=0.01). Conclusion CKD is not infrequent in PsA. Its development is associated with related comorbidities, joint damage and NSAID use. Methotrexate seems to be protective.
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页数:7
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