Park Seokwoo, Kang Eunjeong, Park Sehoon, Kim Yong Chul, Han Seung Seok, Ha Jongwon, Kim Dong Ki, Kim Sejoong, Park Su-Kil, Han Duck Jong, Lim Chun Soo, Kim Yon Su, Lee Jung Pyo, Kim Young Hoon
Departments of Biomedical Sciences.
Internal Medicine, and.
J Am Soc Nephrol. 2017 Jun;28(6):1886-1897. doi: 10.1681/ASN.2016070793. Epub 2016 Dec 28.
Metabolic acidosis (MA), indicated by low serum total CO (TCO) concentration, is a risk factor for mortality and progressive renal dysfunction in CKD. However, the long-term effects of MA on kidney transplant recipients (KTRs) are unclear. We conducted a multicenter retrospective cohort study of 2318 adult KTRs, from January 1, 1997 to March 31, 2015, to evaluate the prevalence of MA and the relationships between TCO concentration and clinical outcomes. The prevalence of low TCO concentration (<22 mmol/L) began to increase in KTRs with eGFR<60 ml/min per 1.73 m and ranged from approximately 30% to 70% in KTRs with eGFR<30 ml/min per 1.73 m Multivariable Cox proportional hazards models revealed that low TCO concentration 3 months after transplant associated with increased risk of graft loss (hazard ratio [HR], 1.74%; 95% confidence interval [95% CI], 1.26 to 2.42) and death-censored graft failure (DCGF) (HR, 1.66; 95% CI, 1.14 to 2.42). Cox regression models using time-varying TCO concentration additionally demonstrated significant associations between low TCO concentration and graft loss (HR, 3.48; 95% CI, 2.47 to 4.90), mortality (HR, 3.16; 95% CI, 1.77 to 5.62), and DCGF (HR, 3.17; 95% CI, 2.12 to 4.73). Marginal structural Cox models adjusted for time-varying eGFR further verified significant hazards of low TCO concentration for graft loss, mortality, and DCGF. In conclusion, MA was frequent in KTRs despite relatively preserved renal function and may be a significant risk factor for graft failure and patient mortality, even after adjusting for eGFR.
代谢性酸中毒(MA)以血清总二氧化碳(TCO)浓度降低为指标,是慢性肾脏病(CKD)患者死亡和进行性肾功能不全的危险因素。然而,MA对肾移植受者(KTRs)的长期影响尚不清楚。我们对1997年1月1日至2015年3月31日期间的2318例成年KTRs进行了一项多中心回顾性队列研究,以评估MA的患病率以及TCO浓度与临床结局之间的关系。在估算肾小球滤过率(eGFR)<60 ml/(min·1.73 m²)的KTRs中,低TCO浓度(<22 mmol/L)的患病率开始上升,在eGFR<30 ml/(min·1.73 m²)的KTRs中,这一患病率约为30%至70%。多变量Cox比例风险模型显示,移植后3个月时低TCO浓度与移植肾丢失风险增加相关(风险比[HR]为1.74;95%置信区间[95%CI]为1.26至2.42),以及与死亡删失的移植肾失功(DCGF)相关(HR为1.66;95%CI为1.14至2.42)。使用随时间变化的TCO浓度的Cox回归模型进一步表明,低TCO浓度与移植肾丢失(HR为3.48;95%CI为2.47至4.90)、死亡率(HR为3.16;95%CI为1.77至5.62)和DCGF(HR为3.17;95%CI为2.12至4.73)之间存在显著关联。针对随时间变化的eGFR进行调整的边际结构Cox模型进一步证实了低TCO浓度对移植肾丢失、死亡率和DCGF具有显著风险。总之,尽管肾功能相对保留,但MA在KTRs中很常见,并且即使在调整eGFR后,MA也可能是移植肾失功和患者死亡的重要危险因素。