Ingrasciotta Ylenia, Sultana Janet, Giorgianni Francesco, Fontana Andrea, Santangelo Antonio, Tari Daniele Ugo, Santoro Domenico, Arcoraci Vincenzo, Perrotta Margherita, Ibanez Luisa, Trifirò Gianluca
Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Unit of Biostatistics, IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo (FG), Italy.
PLoS One. 2015 Apr 16;10(4):e0122899. doi: 10.1371/journal.pone.0122899. eCollection 2015.
Non-steroidal anti-inflammatory agents (NSAIDs) are known to be associated with renal damage. No clear evidence exists regarding differential risk of chronic kidney disease (CKD), specifically, across various NSAIDs.
The aim of this population-based case-control study was to evaluate the association between use of individual NSAIDs and risk of CKD in a general population of Southern Italy.
A nested case-control study was carried out using the general practice Arianna database, identifying incident CKD patients as cases and matched controls from 2006 to 2011. The date of first CKD diagnosis was defined as the index date (ID). Conditional logistic regressions were performed to estimate the risk of CKD associated with NSAIDs by class and individual drugs as compared to non-use during different time windows (within one year, six or three months prior to ID), with the latter being defined as current users. Among current users, the effect of cumulative exposure to these drugs was evaluated.
Overall, 1,989 CKD cases and 7,906 matched controls were identified. A statistically significant increase in the risk of CKD was found for current users of oxicams (adjusted OR: 1.68; 95% CI: 1.15-2.44) and concerning individual compounds, for ketorolac (adj. OR: 2.54; 95% CI: 1.45-4.44), meloxicam (adj. OR: 1.98; 95% CI: 1.01-3.87) and piroxicam (adj. OR: 1.95; 95% CI: 1.19-3.21).
The risk of CKD varies across individual NSAIDs. Increased risk has been found for ketorolac, which may precipitate subclinical CKD through acute renal damage, and long-term exposure to oxicams, especially meloxicam and piroxicam.
已知非甾体抗炎药(NSAIDs)与肾损伤有关。关于慢性肾脏病(CKD)的差异风险,特别是在各种NSAIDs之间,尚无明确证据。
这项基于人群的病例对照研究的目的是评估意大利南部普通人群中使用个体NSAIDs与CKD风险之间的关联。
利用阿丽亚娜全科医疗数据库开展一项巢式病例对照研究,将2006年至2011年期间确诊的CKD患者作为病例,并匹配对照。首次CKD诊断日期定义为索引日期(ID)。进行条件逻辑回归,以估计与未使用NSAIDs相比,在不同时间窗(ID前一年内、六个月或三个月)使用NSAIDs按类别和个体药物导致CKD的风险,后者定义为当前使用者。在当前使用者中,评估了这些药物累积暴露的影响。
总体而言,共识别出1989例CKD病例和7906例匹配对照。发现昔康类当前使用者的CKD风险有统计学意义的增加(调整后的比值比:1.68;95%置信区间:1.15 - 2.44),就个体化合物而言,酮咯酸(调整后的比值比:2.54;95%置信区间:1.45 - 4.44)、美洛昔康(调整后的比值比:1.98;95%置信区间:1.01 - 3.87)和吡罗昔康(调整后的比值比:1.95;95%置信区间:1.19 - 3.21)的风险增加。
CKD风险在个体NSAIDs之间存在差异。已发现酮咯酸风险增加,其可能通过急性肾损伤促使亚临床CKD发生,以及长期暴露于昔康类,尤其是美洛昔康和吡罗昔康。