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©The Author(s) 2015.
World J Nephrol. Jul 6, 2015; 4(3): 324-329
Published online Jul 6, 2015. doi: 10.5527/wjn.v4.i3.324
Published online Jul 6, 2015. doi: 10.5527/wjn.v4.i3.324
Author | Numerosity | Average follow-up | Major findings | Ref. |
Gerhardt et al (1999) | 375 | 5 yr | Hyperuricemia (> 8.0 mg/dL in men and > 6.2 mg/dL in women), associated with reduced graft survival | [12] |
Armstrong et al (2005) | 90 | 2.2 yr | UA independent predictor of follow-up eGFR, but not of eGFR change over time | [13] |
Akgul et al (2007) | 133 | 3 yr | No association found between serum UA and the development of chronic allograft nephropathy | [14] |
Saglam et al (2008) | 34 | Not reported | Serum UA associated to development of cyclosporine A nephropathy (biopsy proven) | [15] |
Akalin et al (2008) | 307 | 4.3 yr | Hyperuricemia 6 mo after transplantation significantly associated with new cardiovascular events and graft dysfunction | [16] |
Bandukwala et al (2009) | 405 | 2 yr | Hyperuricemia associated with cardiovascular events, and, inversely with eGFR | [17] |
Meyer-Kriesche et al (2009) | 1645 | 3 yr | UA levels one month after transplantation not associated with follow-up eGFR, after adjustment for baseline renal function | [20] |
Karbowska et al (2009) | 78 | Not reported | Hyperuricemia associated with markers of endothelial dysfunction and inflammation | [19] |
Min et al (2009) | 368 | 58 ± 23 mo | Early-onset moderate-to-severe hyperuricaemia (serum UA ≥ 8.0 mg/dL) was found to be a significant risk factor for chronic allograft nephropathy (P = 0.035) and a poorer graft survival (P = 0.026) by multivariate analysis, whereas mild hyperuricaemia was not | [18] |
Haririan et al (2010) | 212 | 68 ± 27 mo | Serum UA during the first 6 mo postransplant, is an independent predictor of graft survival | [21] |
Kim et al (2010) | 356 | 102.6 ± 27.2 mo | Patients with eGFR> 60 mL/min per 1.73 m2. Hyperuricemia associated with decreased eGFR | [10] |
Boratyńska et al (2010) | 100 | 34 ± 12 mo | Serum UA not associated to graft survival during 30 mo of follow-up | [22] |
Chung et al (2011) | 351 | 10 yr | Hyperuricemia increased risk of cardiovascular complication; graft survival at 5 and 10 yr lower in hyperuricemic vs normouricemic patients (89% vs 96% and 81% vs 93% respectively, P = 0.02) | [23] |
Kim et al (2011) | 556 | Not reported | Serum UA levels affect graft function, even after adjustment for baseline eGFR | [24] |
Wang et al (2011) | 524 | 10 yr | Retrospective study: UA significantly lower in patients with longer graft survival | [25] |
Park et al (2013) | 428 | 120 ± 58 mo | Serum UA associated with allograft loss, but rate of eGFR decline more potent predictor | [26] |
Choi et al (2013) | 378 | 10 yr | Graft survival (living donor renal transplantation) 88.6% in normouricemic vs 78.8% in hyperuricemic patients | [27] |
Dahle et al (2014) | 2200 | 7.4 yr | Highest serum UA quintile independently associated with increased HR (2.87, 95%CI: 1.55-5.32) of cardiovascular and all-cause (1.55, 95%CI: 1.09-2.25) mortality | [28] |
Hart et al (2014) | 149 | 5 yr | Post-hoc study of the ABCAN trial. Serum UA independently associated with increased odds of composite outcome of doubling of interstitium or ESRD from Interstitial Fibrosis/Tubular Atrophy, after adjusting for eGFR | [29] |
Weng et al (2014) | 880 | 43.3 ± 26.3 mo | Hyperuricemia associated with poorer graft survival (60.5% vs 75.8%, P = 0.007), no difference in all-cause mortality | [30] |
Boratyńska et al (2014) | 637 | 10 yr | Retrospective study. Hyperuricemia associated with chronic allograft dysfunction | [31] |
Weng et al (2014) | 124 | 14.3 mo | Patients undergoing biopsies for acute allograft dysfunction. Hyperuricemia associated with a greater cumulative incidence at one year of doubling serum creatinine or graft loss (29.8% vs 14.9%, P = 0.02) compared to normouricemia | [32] |
- Citation: Bellomo G. Asymptomatic hyperuricemia following renal transplantation. World J Nephrol 2015; 4(3): 324-329
- URL: https://www.wjgnet.com/2220-6124/full/v4/i3/324.htm
- DOI: https://dx.doi.org/10.5527/wjn.v4.i3.324