Evidence map›Paper›PMID 40287983›Full record

ArticleThe Journal of international medical research2025

Impact of preoperative complement-dependent cytotoxicity crossmatch on postoperative outcomes in kidney transplant recipients: A retrospective analysis.

Chonghe Xu, Siqi Xie, Meiyi Lu, Wei Xu, Mei Zhu

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Article in The Journal of international medical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Chonghe XuBeijing Friendship Hospital, Capital Medical University, Beijing, PR China.
Siqi XieDepartment of Clinical Laboratory, The Affiliated Chaohu Hospital of Anhui Medical University, ChaoHu, Anhui, PR China.
Meiyi LuDepartment of Clinical Laboratory, The Affiliated Chaohu Hospital of Anhui Medical University, ChaoHu, Anhui, PR China.
Wei XuDepartment of Blood Transfusion, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, PR China.
Mei ZhuDepartment of Clinical Laboratory, The Affiliated Chaohu Hospital of Anhui Medical University, ChaoHu, Anhui, PR China.ORCID 0000-0003-3130-3672

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ObjectivesThe aim of the present study was to compare the differences in clinical outcomes within 6 months postoperatively between a complement-dependent cytotoxicity <10% group of low-risk kidney transplant patients and a complement-dependent cytotoxicity ≥10% group of relatively high-risk patients.MethodsThe clinical data of 330 patients who underwent kidney transplantation were retrospectively analyzed. The patients were divided into three groups according to the results of complement-dependent cytotoxicity crossmatch: (a) group 1 (complement-dependent cytotoxicity ≥10%); (b) group 2a (5% ≤ complement-dependent cytotoxicity < 10%); and (c) group 2b (complement-dependent cytotoxicity <5%). The clinical outcomes were compared between the three groups.ResultsSignificant differences were noted in serum creatinine levels and estimated glomerular filtration rate between groups 2a and 2b on days (D) 1, 2, 3, and 7 (P < 0.005). From postoperative D1 to month (M) 6, a significant difference (P < 0.05) was noted in urea levels between the three groups. On D3, blood glucose levels were significantly lower in group 2b than in group 2a (P < 0.001); at M6, group 2b exhibited lower blood glucose levels than group 1 (P = 0.043). On D2, group 2b had a lower neutrophil percentage than group 1 (P < 0.05), which was significantly different from those of groups 1 and 2a on D3 (P < 0.05). The percentage and absolute number of lymphocytes in group 2b were significantly higher than those in group 1 (P < 0.01) on D1 and D2. The percentage and absolute number of lymphocytes were significantly higher in group 2b than in groups 1 and 2a on D3 and D7 (P < 0.05).ConclusionsComplement-dependent cytotoxicity <10%, particularly complement-dependent cytotoxicity <5%, was associated with superior attributes compared with complement-dependent cytotoxicity ≥10% in terms of most aspects of postoperative recovery and low incidence of adverse events. However, delayed graft function rate was highest in the complement-dependent cytotoxicity of 5%-10% group. The source of donor kidneys was the most important factor influencing delayed graft function, and a larger cohort with a longer follow-up period may be needed to verify the tendency.

Indexed as

Complement System ProteinsGraft RejectionHistocompatibility TestingKidney TransplantationAdultCreatinineFemaleGlomerular Filtration RateGraft SurvivalHumansMaleMiddle AgedPostoperative PeriodRetrospective StudiesTransplant RecipientsTreatment OutcomeComplement System ProteinsCreatinineclinical outcomescomplement-dependent cytotoxicity crossmatchdelayed graft functionKidney transplantationprognosis

Identifiers

PMID40287983
PMCPMC12053274

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.