Vitamin D deficiency may predispose patients to increased risk of kidney transplant rejection.

Semih Buyukdemirci, Ebru Gok Oguz, Sanem Guler Cimen, Hatice Sahin, Sertac Cimen, Mehmet Deniz Ayli
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引用次数: 1

Abstract

Background: Vitamin D deficiency occurs in more than 80% of kidney transplant recipients. Its immunomodulatory effects can predispose transplant recipients to rejection and chronic allograft nephropathy (CAN). This study determined the association between serum 25 (OH) vitamin D, biopsy-proven allograft rejection, and CAN rates.

Aim: To determine the relationship between serum 25 (OH) vitamin D level and biopsy-proven allograft rejection and CAN rate in renal transplant recipients.

Methods: Adult renal transplant recipients followed at the clinic between January 2013 and 2018 were included. Recipients requiring graft biopsy due to declined function, hematuria, and proteinuria were reviewed. The two groups were compared regarding collected data, including the biopsy results, immunologic parameters, vitamin D, parathyroid hormone (PTH), phosphorus, albumin levels, and graft function tests.

Results: Fifty-two recipients who underwent graft biopsy met the inclusion criteria. In all, 14 recipients had a vitamin D level > 15 ng/mL (group 1) vs ≤ 15 ng/mL (group 2) in 38. In total, 27 patients had biopsy-proven rejection, and 19 had CAN. There was only 1 recipient with biopsy-proven rejection in group 1, whereas there were 24 patients with rejection in group 2. The rejection rate was significantly higher in group 2 than in group 1 (P < 0.001). Four patients were diagnosed with CAN in group 1 vs fifteen in group 2. There was no significant difference in the CAN rate between the two groups. PTH was higher at the time of graft biopsy (P = 0.009, P = 0.022) in group 1 with a mean of 268 pg/mL. Donor-specific antibodies were detected in 14 (56.0%) of the recipients with rejection. Vitamin D level was 9.7 ± 3.4 ng/mL in the rejection group vs 14.7 ± 7.2 in the non-rejection group; this difference was statistically significant (P = 0.003). The albumin levels were significantly lower in patients with rejection than in those without rejection (P = 0.001). In univariate regression analysis of risk factors affecting rejection, sex, serum vitamin D, phosphorus and albumin were found to have an impact (P = 0.027, P = 0.007, P = 0.023, P = 0.008). In multivariate regression analysis, the same factors did not affect rejection.

Conclusion: The serum 25 (OH) vitamin D level in kidney transplant recipients remained low. Although low serum vitamin D level emerged as a risk factor for rejection in univariate analysis, this finding was not confirmed by multivariate analysis. Prospective studies are required to determine the effect of serum vitamin D levels on allograft rejection.

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维生素D缺乏可能增加患者肾移植排斥反应的风险。
背景:80%以上的肾移植受者缺乏维生素D。其免疫调节作用可使移植受者易发生排斥反应和慢性同种异体肾病(can)。本研究确定了血清25 (OH)维生素D、活检证实的同种异体移植排斥反应和CAN率之间的关系。目的:探讨肾移植受者血清25 (OH)维生素D水平与活检证实的同种异体移植排斥反应和CAN发生率的关系。方法:纳入2013年1月至2018年1月在诊所随访的成人肾移植受者。由于功能下降、血尿和蛋白尿而需要移植物活检的受者进行了回顾。比较两组收集的数据,包括活检结果、免疫参数、维生素D、甲状旁腺激素(PTH)、磷、白蛋白水平和移植物功能测试。结果:52例接受移植物活检的受者符合纳入标准。总共有14名接受者的维生素D水平> 15 ng/mL(第一组),而38名接受者的维生素D水平≤15 ng/mL(第二组)。总共有27名患者有活检证实的排斥反应,19名患者有CAN。在第一组中只有1例接受者活检证实有排斥反应,而在第二组中有24例患者有排斥反应。2组排斥反应率明显高于1组(P < 0.001)。1组诊断为CAN患者4例,2组诊断为15例。两组间CAN发生率无显著性差异。PTH在移植物活检时较高(P = 0.009, P = 0.022),组1平均为268 pg/mL。在14例(56.0%)排斥受体中检测到供体特异性抗体。排斥反应组维生素D水平为9.7±3.4 ng/mL,非排斥反应组为14.7±7.2 ng/mL;差异有统计学意义(P = 0.003)。排斥反应患者的白蛋白水平明显低于无排斥反应患者(P = 0.001)。单因素回归分析发现,性别、血清维生素D、磷和白蛋白对排斥反应有影响(P = 0.027, P = 0.007, P = 0.023, P = 0.008)。在多元回归分析中,相同的因素不影响排斥反应。结论:肾移植受者血清25 (OH)维生素D水平维持在较低水平。虽然低血清维生素D水平在单因素分析中被认为是排斥反应的危险因素,但这一发现并未被多因素分析证实。需要前瞻性研究来确定血清维生素D水平对同种异体移植排斥反应的影响。
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