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单次排尿中肾上腺素和去甲肾上腺素检测对诊断嗜铬细胞瘤的效能。

Efficacy of single-voided urine metanephrine and normetanephrine assay for diagnosing pheochromocytoma.

作者信息

Ito Y, Obara T, Okamoto T, Kanbe M, Tanaka R, Iihara M, Okamoto J, Yamazaki K, Jibiki K

机构信息

Department of Endocrine Surgery, Tokyo Women's Medical College, Kawada-cho 8-1, Shinjuku-ku, Tokyo 162, Japan.

出版信息

World J Surg. 1998 Jul;22(7):684-8. doi: 10.1007/s002689900453.

Abstract

Urinary catecholamines (CAs) and their metabolites are usually measured during the process of diagnosing pheochromocytoma (pheo), but a 24-hour urine collection is not convenient for outpatients. Since 1987 we have utilized "spot" urine metanephrine (MN) and normetanephrine (NMN) assays for management of patients with pheo or adrenal incidentaloma. MN and NMN were measured by radioimmunoassay in 82 patients with surgically proved pheo and 15 patients with incidentaloma. In 10 patients with pheo, MN and NMN were measured with fractional every-3-hour urine samples, which were accumulated and then measured as a 24-hour urinary specimen. Fractions of 3-hour MN and NMN excretion were constant (MN 98.5 +/- 9.6%, NMN 97.6 +/- 10.8%; 24-hour MN and NMN 100%). The average levels of MN and NMN in patients with pheo were 6801 ng/mg creatinine (Cr) (range 93-88,248, median 1426) and 5627 ng/mg Cr (range 219-31,528, mean 3190), whereas the MN and NMN levels in patients with incidentaloma were 123 ng/mg Cr (range 36-246, mean 133) and 251 ng/mg Cr (range 84-472, mean 220), respectively. When we selected a cutoff value for MN + NMN of 1000 ng/mg Cr, the sensitivity was 97.6% and the specificity 100% for diagnosing pheo. When the standard was set as > 500 ng/mg Cr for either MN or NMN, both the sensitivity and specificity were 100%. The assay for MN and NMN is simple and effective, not only for screening but for diagnosing pheo and managing incidentaloma.

摘要

尿儿茶酚胺(CAs)及其代谢产物通常在嗜铬细胞瘤(pheo)的诊断过程中进行检测,但24小时尿液收集对于门诊患者来说并不方便。自1987年以来,我们一直使用“随机”尿间甲肾上腺素(MN)和去甲间甲肾上腺素(NMN)检测来管理嗜铬细胞瘤或肾上腺偶发瘤患者。对82例经手术证实的嗜铬细胞瘤患者和15例偶发瘤患者采用放射免疫分析法测定MN和NMN。对10例嗜铬细胞瘤患者,每隔3小时采集一次尿液样本进行MN和NMN检测,将这些样本累积起来后作为24小时尿液标本进行测定。3小时MN和NMN排泄分数是恒定的(MN为98.5±9.6%,NMN为97.6±10.8%;24小时MN和NMN为100%)。嗜铬细胞瘤患者MN和NMN的平均水平分别为6801 ng/mg肌酐(Cr)(范围93 - 88,248,中位数1426)和5627 ng/mg Cr(范围219 - 31,528,均值3190),而偶发瘤患者的MN和NMN水平分别为123 ng/mg Cr(范围36 - 246,均值133)和251 ng/mg Cr(范围84 - 472,均值220)。当我们将MN + NMN的临界值设定为1000 ng/mg Cr时,诊断嗜铬细胞瘤的敏感性为97.6%,特异性为100%。当标准设定为MN或NMN大于500 ng/mg Cr时,敏感性和特异性均为100%。MN和NMN检测简单有效,不仅可用于筛查,还可用于诊断嗜铬细胞瘤和管理偶发瘤。

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