[在诊断嗜铬细胞瘤时测定偏胰高血糖素水平的各种方法的有效性比较]。

Sh Sh Shikhmagomedov, D V Rebrova, L M Krasnov, E A Fedorov, I K Chinchuk, R A Chernikov, V F Rusakov, I V Slepstov, E A Zgoda
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引用次数: 0

摘要

背景:嗜铬细胞瘤(PHEO嗜铬细胞瘤(PHEO)是一种来自肾上腺髓质绒毛组织的肿瘤,能够过度分泌儿茶酚胺。肿瘤分泌的激素增多会导致儿茶酚胺危机,对所有器官和系统产生病理影响。在嗜铬细胞瘤的初步诊断中,确定儿茶酚胺的代谢产物--间甲肾上腺素的水平非常重要。目前,在临床实践中,有多种方法可用于确定这种代谢物的水平:血浆或尿液中、总量或仅游离形式、分馏分析或非分馏分析。目的:比较各种方法确定嗜铬细胞瘤诊断中的甲肾上腺素水平的有效性:对2007年11月至2022年12月期间在皮拉戈夫-圣彼得堡国立大学高级医疗技术诊所接受肾上腺肿瘤初次手术的患者样本进行了一项回顾性单中心队列研究,这些患者在手术治疗前通过了血液或尿液中偏胰高血脂素水平的分析。结果显示,1088 名肾上腺肿瘤患者接受了手术治疗:对1088名接受手术治疗的肾上腺肿瘤患者进行了检查,其中348人经组织学证实患有嗜铬细胞瘤。比较了四种甲肾上腺素检测方法:游离分馏血浆甲肾上腺素(232 例患者)、未分馏每日尿液甲肾上腺素(431 例患者)、分馏每日尿液总甲肾上腺素(427 例患者)和分馏游离每日尿液甲肾上腺素(178 例患者)。对游离分馏血浆甲肾上腺素的分析灵敏度最高(95.4%)。与其他方法不同的是,在嗜铬细胞瘤较小(3 厘米或以下)的患者组中,该分析方法的灵敏度并没有降低。对每日尿液中未分馏的偏胰岛素进行分析的特异性最高(97.8%),而灵敏度在所有检测项目中最低(67.6%)。对分馏的日尿中总偏胰岛素的研究显示出良好的灵敏度和特异性,只是略逊于最佳指标,而对游离的日尿中偏胰岛素的分析则显示出出乎意料的低效率。血液中的甲肾上腺素水平与肿瘤大小呈正相关:根据所获得的数据,可以认为嗜铬细胞瘤初诊的首选检测方法是测定分馏游离血浆中的甲肾上腺素和分馏每日尿液中的总甲肾上腺素,这与相关的临床建议一致。研究发现,肿瘤的大小与上述任何一种方法测定的偏胰岛素水平升高的严重程度相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Comparison of the effectiveness of various methods for determining the level of metanephrines in the diagnosis of pheochromocytomas].

Background: Pheochromocytoma (PHEO) is a tumor from the chromaffin tissue of the adrenal medulla, capable of hyperproduction of catecholamines. The increased production of hormones by the tumor leads to catecholamine crises, which have a pathological effect on all organs and systems. In the primary diagnosis of pheochromocytomas, it is important to determine the level of the metabolite of catecholamines - metanephrines. Currently, in clinical practice, various methods are used to determine the level of this metabolite: in blood plasma or in urine, total or only free form, fractionated analysis or unfractionated.

Aim: Comparison of the effectiveness of various methods for determining the level of metanephrines for the diagnosis of pheochromocytomas.

Materials and methods: A retrospective single-center cohort study was conducted on a sample of patients who were initially operated on for adrenal neoplasm at the Pirogov St. Petersburg State University High Medical Technology Clinic from November 2007 to December 2022 and who passed analysis to determine the level of blood or urine metanephrins before surgical treatment. The results of tests for metanephrine and tumor size were evaluated.

Results: 1088 patients with adrenal neoplasms who underwent surgical treatment were examined, of which 348 had histologically confirmed the presence of pheochromocytoma. Four types of metanephrine assays were compared: free fractionated plasma metanephrines (232 patients), unfractionated daily urine metanephrines (431 patients), fractionated total daily urine metanephrines (427 patients) and fractionated free daily urine metanephrines (178 patients). The greatest sensitivity was demonstrated by the analysis of free fractionated plasma methanephrines (95.4%). Unlike others, the sensitivity of this analysis did not decrease in the group of patients with small pheochromocytomas (3 cm or less). The greatest specificity was demonstrated by the analysis of unfractionated metanephrines in daily urine (97.8%), with the lowest sensitivity among all tests (67.6%). The study of fractionated total daily urine metanephrins showed good results of sensitivity and specificity, only slightly inferior to the best indicators, and the analysis of free daily urine metanephrins demonstrated unexpectedly low efficiency. There is a positive correlation between the level of metanephrine in the blood and the size of the tumor.

Conclusion: Based on the data obtained, the preferred assays for the primary diagnosis of pheochromocytoma can be considered the determination of fractionated free plasma metanephrines and fractionated total daily urine metanephrines, which is consistent with relevant clinical recommendations. It was found that the size of the tumor correlates with the severity of an increase in the level of metanephrins determined by any of the described methods.

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