Impact of Donor Age on Graft Failure After Deceased Donor Liver Transplantation by Donor-Recipient Sex Combinations: An Analysis of the UNOS OPTN Database.

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Sangbin Han, Vatche A Agopian, Justin A Steggerda, Irene K Kim, Alison Sanford, Yi-Te Lee, Ji-Hye Kwon, Jin Soo Rhu, Gaab Soo Kim, Ju-Dong Yang
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引用次数: 0

Abstract

Background Sex disparity has been highlighted in personalized medicine for various human diseases including acute/chronic liver diseases. In the transplant community, greater graft failure risk in female-to-male liver transplantation (LT) has been repeatedly reported, and a recent study in living donor LT reported that the inferiority of female-to-male LT is shown only when donor age is ≤40 y. We aimed to analyze the United Network for Organ Sharing (UNOS) database to test if the poorer outcome of female-to-male LT changes by donor age of 40 y in deceased donor LT, as shown in living donor LT. Methods In this retrospective cohort study, 11,752 adult patients in the UNOS registry who underwent deceased donor LT between 2000-2023 were analyzed. Multivariable analysis was performed to adjust the effects from transplant years, graft ischemia time, disease severity, and others. The primary outcome was graft failure. Results Within the subgroup of recipients with ≤40 y donors, graft failure risk was significantly greater in female-to-male LT than others (vs. female-to-female, HR = 1.43 [1.16-1.76], p < 0.001; vs. male-to-female, HR = 1.46 [1.18-1.81], p < 0.001; vs. male-to-male, HR = 1.26 [1.16-1.49], p = 0.009). In contrast, within the subgroup of recipients with >40 y donors, the risk was comparable between female-to-male LT and other donor-recipient sex groups (vs. female-to-female, p = 0.907; vs. male-to-female, p = 0.781; vs. male-to-male, p = 0.937). We tested various cutoff donor ages and determined that 40 y is the best cutoff value to define the risk subgroup in female-to-male LT. Conclusions In the current study, we found that the sex disparity shown in living donor LT is also observed in deceased donor LT. That is, post-transplant graft failure risk was greater in female-to-male LT than other donor-recipient sex groups only when donor age was ≤40 y. In contrast, graft failure risk was comparable irrespective of donor-recipient sex combinations when donor age was >40 y.

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供者年龄对供者-受者性别组合已故供者肝移植后移植物衰竭的影响:UNOS OPTN数据库的分析
性别差异在包括急性/慢性肝病在内的各种人类疾病的个性化医疗中得到了突出体现。移植社区中,再次移植移植物衰竭更大风险的女性对男性肝移植(LT)已经被多次报道,在活体供肝移植和最近的一项研究报告称,女性对男性的自卑LT显示只有当供体年龄≤40 y。我们旨在分析器官共享联合网络(凯泽本人)数据库来测试如果贫穷的女性对男性LT变化结果供体年龄40 y在死者供体肝移植,方法在这项回顾性队列研究中,分析了2000-2023年间在UNOS登记的11752例接受了已故供体肝移植的成年患者。进行多变量分析以调整移植年份、移植物缺血时间、疾病严重程度等因素的影响。主要结局是移植物衰竭。结果在供体≤40 y的受体亚组中,女性对男性的移植失败风险显著高于其他组(女性对女性,HR = 1.43 [1.16-1.76], p < 0.001;男性对女性,HR = 1.46 [1.18-1.81], p < 0.001;男性对男性,HR = 1.26 [1.16-1.49], p = 0.009)。相比之下,在bbb40 y供者的受体亚组中,女性对男性和其他供者-受体性别组之间的风险相当(与女性对女性相比,p = 0.907;与男性对女性相比,p = 0.781;与男性对男性相比,p = 0.937)。我们对不同的供体年龄进行了测试,确定40岁是定义女转男肝移植风险亚组的最佳临界值。结论在本研究中,我们发现在活体供体肝移植中所显示的性别差异也出现在已故供体肝移植中。即,只有当供体年龄≤40岁时,女性转男性肝移植后移植失败的风险才高于其他供体-受体性别组。当供体年龄为10 ~ 40岁时,移植失败的风险与供体-受体性别组合无关。
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来源期刊
Journal of Personalized Medicine
Journal of Personalized Medicine Medicine-Medicine (miscellaneous)
CiteScore
4.10
自引率
0.00%
发文量
1878
审稿时长
11 weeks
期刊介绍: Journal of Personalized Medicine (JPM; ISSN 2075-4426) is an international, open access journal aimed at bringing all aspects of personalized medicine to one platform. JPM publishes cutting edge, innovative preclinical and translational scientific research and technologies related to personalized medicine (e.g., pharmacogenomics/proteomics, systems biology). JPM recognizes that personalized medicine—the assessment of genetic, environmental and host factors that cause variability of individuals—is a challenging, transdisciplinary topic that requires discussions from a range of experts. For a comprehensive perspective of personalized medicine, JPM aims to integrate expertise from the molecular and translational sciences, therapeutics and diagnostics, as well as discussions of regulatory, social, ethical and policy aspects. We provide a forum to bring together academic and clinical researchers, biotechnology, diagnostic and pharmaceutical companies, health professionals, regulatory and ethical experts, and government and regulatory authorities.
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