Liu Yuguan, Weisberg Lawrence S, Langman Craig B, Logan Amanda, Hunter Krystal, Prasad Deepali, Avila Jose, Venkatchalam Thaliga, Berns Jeffrey S, Handelman Garry J, Sirover William D
University of Massachusetts, Lowell 3 Solomont Way, Lowell, MA 01854, United States.
Cooper Medical School of Rowan University 401 Haddon Avenue, Camden, NJ 08103, United States.
Clin Biochem. 2016 Oct;49(15):1133-1139. doi: 10.1016/j.clinbiochem.2016.05.025. Epub 2016 Jun 3.
Ascorbic acid (AA) supplementation may increase hemoglobin levels and decrease erythropoiesis-stimulating agent dose requirement in patients with end stage renal disease (ESRD). While plasma AA levels >100μM may be supratherapeutic, levels of at least 30μM may be needed to improve wound healing and levels may need to reach 70μM to optimize erythropoiesis. Of concern, oxalate (Ox), an AA metabolite, can accumulate in ESRD. Historically, if plasma Ox levels remain ≥30μM, oxalosis was of concern. Contemporary hemodialysis (HD) efficiencies may decrease the risk of oxalosis by maintaining pre-HD Ox levels <30μM. This study focuses on the plasma Ox levels in HD patients.
A prospective, observational study of 197 HD patients with pre-HD AA levels and pre-HD and post-HD Ox levels.
Mean plasma Ox levels decreased 71% during the intradialytic period (22.3±11.1μM to 6.4±3.2μM, P<0.001). In regression analysis, pre-HD plasma AA levels ≤100μM were not associated with a pre-HD plasma Ox level≥30μM, even if ferritin levels were increased. Pre-HD plasma Ox levels ≥20 or ≥30μM were not associated with lower cumulative 4-year survival.
Pre-HD plasma AA levels up to 100μM in HD patients do not appear to be associated with an increased risk of developing secondary oxalosis, as the corresponding pre-HD plasma Ox level appears to be maintained at tolerable levels.
补充抗坏血酸(AA)可能会提高终末期肾病(ESRD)患者的血红蛋白水平,并降低促红细胞生成素的剂量需求。虽然血浆AA水平>100μM可能超治疗量,但可能需要至少30μM的水平来促进伤口愈合,且可能需要达到70μM才能优化红细胞生成。值得关注的是,AA的代谢产物草酸盐(Ox)可在ESRD患者体内蓄积。从历史上看,如果血浆Ox水平≥30μM,就会担心发生草酸盐中毒。当代血液透析(HD)效率通过将透析前Ox水平维持在<30μM,可能会降低草酸盐中毒风险。本研究聚焦于HD患者的血浆Ox水平。
一项对197例HD患者进行的前瞻性观察研究,测定其透析前AA水平以及透析前和透析后Ox水平。
透析期间血浆Ox平均水平下降了71%(从22.3±11.1μM降至6.4±3.2μM,P<0.001)。回归分析显示,即使铁蛋白水平升高,透析前血浆AA水平≤100μM与透析前血浆Ox水平≥30μM无关。透析前血浆Ox水平≥20或≥30μM与4年累积生存率降低无关。
HD患者透析前血浆AA水平高达100μM似乎与继发性草酸盐中毒风险增加无关,因为相应的透析前血浆Ox水平似乎维持在可耐受水平。