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原发性疾病的影响及关联

Primary disease effects and associations.

作者信息

Katznelson S, McClelland J, Cecka J M

出版信息

Clin Transpl. 1994:403-17.

PMID:7547572
Abstract
  1. Although graft survival for most primary disease processes are similar at one year, significant divergence occurs by 5 years. ALP, IGA, and PC had the highest 5-year graft survival rates (72.8%, 71.2%, and 68.5%, respectively) whereas HTN and NS, the lowest (51.8% and 46.0%, respectively). 2. When primary diseases are grouped by pathogenic, pathophysiologic, and clinical similarities, the group of diseases with systemic manifestations had the lowest 5-year graft survival (55%), and the group including cystic and inherited diseases had the highest 5-year graft survival (69%). Black recipients had a predominance of "systemic" primary diseases (57%). 3. Despite having overall lower graft survival than Whites (p < 0.00001), there was no significant difference between Black and White 3-year graft survival for recipients with PC, ALP, IGA, and SLE. 4. PC recipients enjoyed excellent long-term graft survival (69%). Black recipients with PC had a 5-year graft survival rate of 64.6%. Recipients with PC had decreased posttransplant dialysis need, decreased early rejection rate, and better HLA matching than most other recipients. 5. Recipients with SLE as their primary disease had among the highest fraction of grafts lost to rejection (45.4% of all grafts lost) and the highest pretransplant sensitization rate (59.6%). 6. Recipients with HTN as their primary disease had overall lower 5-year graft survival (58% versus 63% in Whites, 44% versus 47% in Blacks), a lower rate of early allograft function (10% versus 12%, p < 0.00001), and more posttransplant dialysis needs (28.8% of patients requiring dialysis vs 23.5%, p < 0.00001) than recipients without HTN. Blacks with HTN had the lowest long-term graft survival (44.4%) of any other single group. 7. IDDM patients who expressed DR3 and/or DR4 alleles had significantly higher graft survival than patients without these DR groups. Whites expressing DR3 and DR4 and DR3 or DR4 alleles had better overall HLA matching (p < 0.001) and graft survival (75.4% and 70.7% versus 58.5% and 65.1%, p < 0.00001) than Blacks with similar DR expression. 8. SPK recipients had better 5-year graft survival than KAT recipients (66.2% versus 54.6%, p < 0.000001). This effect is most likely due to the selection of "better" lower-risk patients for SPK grafts.
摘要
  1. 尽管大多数原发性疾病过程的移植物存活率在1年时相似,但到5年时会出现显著差异。碱性磷酸酶(ALP)、免疫球蛋白A(IGA)和胰肾联合移植(PC)的5年移植物存活率最高(分别为72.8%、71.2%和68.5%),而高血压(HTN)和肾病综合征(NS)的5年移植物存活率最低(分别为51.8%和46.0%)。2. 当原发性疾病按致病、病理生理和临床相似性分组时,有全身表现的疾病组5年移植物存活率最低(55%),包括囊性和遗传性疾病的组5年移植物存活率最高(69%)。黑人受者中“全身性”原发性疾病占主导(57%)。3. 尽管总体移植物存活率低于白人(p<0.00001),但对于接受PC、ALP、IGA和系统性红斑狼疮(SLE)的受者,黑人与白人的3年移植物存活率没有显著差异。4. 接受PC移植的受者享有出色的长期移植物存活率(69%)。患有PC的黑人受者5年移植物存活率为64.6%。与大多数其他受者相比,接受PC移植的受者移植后透析需求减少,早期排斥率降低,且HLA匹配更好。5. 以SLE为原发性疾病的受者中,因排斥反应而丢失的移植物比例最高(占所有丢失移植物的45.4%),移植前致敏率也最高(59.6%)。6. 以HTN为原发性疾病的受者总体5年移植物存活率较低(白人中为58%对63%,黑人中为44%对47%),早期移植肾功能恢复率较低(10%对12%,p<0.00001),移植后透析需求更多(28.8%的患者需要透析,而无HTN的受者为23.5%,p<0.00001)。患有HTN的黑人长期移植物存活率是所有其他单一组中最低的(44.4%)。7. 表达DR3和/或DR4等位基因的1型糖尿病(IDDM)患者的移植物存活率显著高于没有这些DR组的患者。表达DR3和DR4以及DR3或DR4等位基因的白人总体HLA匹配更好(p<0.001),移植物存活率也更高(75.4%和70.7%,而类似DR表达的黑人分别为58.5%和65.1%,p<0.00001)。8. 同时进行胰肾联合移植(SPK)的受者5年移植物存活率高于肾移植后胰腺移植(KAT)受者(66.2%对54.6%,p<0.000001)。这种效应很可能是由于为SPK移植选择了“更好的”低风险患者。

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