是否有必要修改慢性肾病患者前列腺特异性抗原的正常水平?

Q4 Medicine
Anahita Ansari Djafari, B. Javanmard, AmirHossein Eslami, Esmat Ghanei, Zahra Davoudi, Seyyed Ali Hojjati, Mahboobeh Freidoon
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引用次数: 0

摘要

背景:肾功能减退的患者通常会表现出某些肿瘤标志物水平升高。前列腺特异性抗原(PSA)是由前列腺上皮细胞产生的一种糖蛋白抗原,属于组织钙化酶家族成员。研究目的本研究旨在探讨慢性肾脏病(CKD)患者体内游离和总 PSA 水平、肾小球滤过率(GFR)和体重指数(BMI)之间的潜在关系。研究方法这项横断面调查包括 152 名符合纳入标准的男性 CKD 患者。在患者初次就诊和登记后,测量了游离和总 PSA、血清肌酐和血清总蛋白的水平。随后,使用 Cockcroft 公式计算了所有患者的 GFR。统计分析使用 SPSS 软件进行。结果参与者的平均年龄为 58.5 ± 17.6 岁。此外,游离和总 PSA 的平均水平与 GFR、BMI 和血清肌酐清除率之间呈反比关系。结论:研究结果表明,游离和总 PSA 水平与 GFR 和 BMI 之间存在反比关系。因此,肾功能障碍会严重影响 PSA 水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Is It a Necessity to Revise Normal Level of Prostate-Specific Antigen in Patients with Chronic Kidney Disease?
Background: Typically, patients with decreased renal function exhibit elevated levels of certain tumor markers. Prostate-specific antigen (PSA), a glycoprotein antigen produced by the prostate gland's epithelial cells and a member of the tissue kallikrein family, is among them. Objectives: This study aimed to investigate the potential relationship between free and total PSA levels, glomerular filtration rate (GFR), and Body Mass Index (BMI) in patients with chronic kidney disease (CKD). Methods: This cross-sectional investigation included 152 male CKD patients who met the inclusion criteria. Following the initial patient visits and enrollment, levels of free and total PSA, serum creatinine, and serum total protein were measured. Subsequently, GFR was calculated for all patients using Cockcroft's formula. Statistical analysis was performed using SPSS software. Results: The mean age of the participants was 58.5 ± 17.6 years. Furthermore, there were inverse relationships observed between the mean levels of free and total PSA with GFR, BMI, and serum creatinine clearance. Conclusions: The study's findings reveal inverse relationships between free and total PSA levels and GFR and BMI. Therefore, renal dysfunction can significantly influence PSA levels.
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来源期刊
Nephro-urology Monthly
Nephro-urology Monthly Medicine-Urology
CiteScore
0.40
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0.00%
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26
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