Department of Nephrology and Transplantation, Hôpital Necker, APHP. Université de Paris Cité, France.
Department of Nephrology, CHU Poitiers, Vienne, France. Centre de référence « Amylose AL et autres maladies à dépôts d'immunoglobuline monoclonales».
Nephrol Dial Transplant. 2023 Dec 20;39(1):64-73. doi: 10.1093/ndt/gfad144.
Because of increased access to kidney transplantation in elderly subjects, the prevalence of monoclonal gammopathies of unknown significance (MGUS) in kidney transplantation (KT) is growing. However, little is known about the consequences of MGUS on long-term outcomes.
We identified 70 recipients with MGUS present at transplantation (KTMG) and 114 patients with MGUS occurring after KT (DNMG), among 3059 patients who underwent a KT in two French kidney transplantation centers. We compared outcomes of KTMG with those of matched controls.
Baseline characteristics were similar except for an older age in KTMG compared with the DNMG group (62 vs 57 years, P = .03). Transient MGUS occurred more frequently in DNMG patients (45% vs 24%, P = .007). When compared with matched controls without MGUS, KTMG patients showed higher frequency and earlier post-transplant solid cancers (15% vs 5%, P = .04) and a trend for more bacterial infections (63% vs 48%, P = .08), without difference regarding patient and graft survival, rejection episodes or hematological complications. KTMG patients with an abnormal kappa/lambda ratio and/or severe hypogammaglobulinemia at the time of KT experienced shorter overall survival.
MGUS detection at the time of KT is neither associated with a higher occurrence of graft rejection, nor adversely affects graft or overall survival. MGUS should not contraindicate KT. However, MGUS at the time of KT may be associated with higher risk of early neoplastic and infectious complications and warrants prolonged surveillance. Measurement of serum free light chain should be performed before transplant to refine the risk evaluation of KTMG patients and propose personalized follow-up and immunosuppression.
由于老年人接受肾移植的机会增加,肾移植(KT)中不明意义的单克隆丙种球蛋白血症(MGUS)的患病率正在上升。然而,对于 MGUS 对长期结果的影响知之甚少。
我们在两个法国肾脏移植中心的 3059 名接受 KT 的患者中,确定了 70 名移植时存在 MGUS(KTMG)的受者和 114 名 KT 后发生 MGUS(DNMG)的患者。我们比较了 KTMG 与匹配对照者的结局。
除 KTMG 组年龄大于 DNMG 组(62 岁比 57 岁,P = 0.03)外,基线特征相似。DNMG 患者更常发生短暂性 MGUS(45%比 24%,P = 0.007)。与无 MGUS 的匹配对照者相比,KTMG 患者发生实体癌的频率更高,发生时间更早(15%比 5%,P = 0.04),细菌感染的趋势更高(63%比 48%,P = 0.08),但患者和移植物存活率、排斥反应发作或血液学并发症无差异。在 KT 时存在异常κ/λ比值和/或严重低丙种球蛋白血症的 KTMG 患者总生存时间更短。
在 KT 时检测到 MGUS 既不会增加移植物排斥的发生,也不会对移植物或总生存产生不利影响。MGUS 不应成为 KT 的禁忌证。然而,KT 时的 MGUS 可能与早期肿瘤和感染并发症的风险增加相关,需要进行长期监测。在移植前应进行血清游离轻链检测,以完善 KTMG 患者的风险评估,并提出个性化随访和免疫抑制方案。