IFTA 病灶密度:肾移植活组织切片纤维化的一种未被发现的高度预后测量方法。

IF 3.2 Q1 UROLOGY & NEPHROLOGY Kidney360 Pub Date : 2024-07-18 DOI:10.34067/KID.0000000000000514
Aleksandar Denic, Andrew D Rule, Walter D Park, Byron H Smith, Mateo Velasquez Meija, Aleksandra Kukla, Joseph P Grande, Mark D Stegall
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引用次数: 0

摘要

背景:肾间质纤维化/肾小管萎缩(IFTA)的收缩可能导致IFTA%不能充分反映肾小球丧失的严重程度。IFTA病灶密度较高是预测原生肾脏进展性慢性肾病的重要指标,而与IFTA%无关:我们研究了 2000-2013 年间接受肾移植的受者,他们接受了为期 5 年的肾活检监测和后续随访。我们从病理报告中获得了 Banff ci 评分(间质纤维化)。活组织切片数字化后,我们在单个三色染色切片上追踪皮质面积和每个明显的 IFTA 病灶。计算IFTA面积百分比和IFTA病灶密度(IFTA病灶数/皮质面积)。通过Cox模型评估了5年活检后,以Banff ci评分、形态学%IFTA和IFTA病灶密度为死亡剪除因素的移植物失败风险:结果:在5年的随访中,835名肾脏受者中有58例死亡剪除的异体移植物失败。失败移植物的活检组织具有较高的平均 Banff ci 评分(1.5 vs 0.7,pConclusions):IFTA病灶密度的形态学特征是目前用于肾脏纤维化分级的Banff分级方法中无法捕捉到的、经死亡筛查的同种异体移植物失败的有力预测因素。
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IFTA Foci Density: An Unrecognized Highly Prognostic Measurement of Fibrosis in Kidney Transplant Biopsies.

Background: Contraction of interstitial fibrosis/tubular atrophy (IFTA) may cause %IFTA to under-represent the severity of nephron loss. Higher density of IFTA foci is an important predictor of progressive chronic kidney disease in native kidneys independent of %IFTA.

Methods: We studied kidney transplant recipients transplanted between 2000-2013 who had a 5-year surveillance kidney biopsy and subsequent follow-up. Banff ci score (interstitial fibrosis) was obtained from the pathology reports. After digitizing the biopsies, we traced cortex area and each distinct IFTA focus on a single trichrome-stained section. Percent IFTA area and IFTA foci density (count of IFTA foci/cortex area) were calculated. Cox models assessed the risk of death-censored graft failure after the 5-year biopsy with Banff ci score, morphometric %IFTA, and IFTA foci density.

Results: There were 58 death-censored allograft failures among 835 kidney recipients during the 5 years of follow-up. Biopsies from grafts that failed had higher mean Banff ci score (1.5 vs 0.7, p<0.0001), %IFTA (22.2% vs 7.0%, p<0.0001), and IFTA foci density (1.3 vs. 0.4 per mm2, p<0.001). After adjusting for other Banff scores or clinical variables, Banff ci did not correlate with allograft failure, but both higher %IFTA (HR=1.56, p<0.0001) and higher IFTA foci density (HR=2.34, p<0.001) did. All but 4 allograft failures by 10 years had biopsies in the top quartile of either %IFTA or IFTA foci density at 5 years. A model using just these two morphometric measures without clinical characteristics resulted in a c-statistic of 0.891 with respect to allograft failure.

Conclusions: Morphometric characterization of IFTA foci density is a strong predictor of death censored allograft failure not captured in current Banff classification for grading of kidney fibrosis.

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Kidney360
Kidney360 UROLOGY & NEPHROLOGY-
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