UpToDate
Official reprint from UpToDate®
www.uptodate.com ©2017 UpToDate®

肾衰竭患者的血清酶

Authors
Neil S Sanghani, MD
Ramesh Soundararajan, MD, FACP
Thomas A Golper, MD
Section Editor
Jeffrey S Berns, MD
Deputy Editor
Alice M Sheridan, MD
Translators
路万虹, 副主任医师

引言

终末期肾病(end-stage renal disease, ESRD)患者的血清酶通常异常。这部分是由于肾脏排泄功能丧失和频繁出现的多种合并症。由于很多疾病的诊断是基于发现这些酶水平升高,缺乏关于各种疾病状态下不同酶血清浓度的知识就会阻碍我们对ESRD患者进行准确的临床评估。

本文将总结在透析患者中血清酶的应用和酶浓度变化的意义。有关肾衰竭患者中血清心肌酶的讨论参见其他专题。 (参见“肾衰竭患者的血清心脏生物标志物”)

肝酶

最常用于帮助评估肝胆系统疾病诊断的血清酶包括转氨酶、碱性磷酸酶和γ谷氨酰转肽酶(gammaglutamyl transpeptidase, GGT)。

转氨酶 — 常规测量血清天冬氨酸转氨酶和丙氨酸转氨酶[AST(SGOT)和ALT(SGPT)]浓度来评估伴或不伴肾衰竭患者的肝功能。正常情况下,转氨酶在循环中的浓度较低,通常小于40U/L。 (参见“肝生化和肝功能试验异常患者的评估”,关于‘肝酶’一节)

长期透析患者和慢性肾衰竭患者的血清转氨酶浓度都主要处于正常范围的低限[1-4]。尽管确切原因尚不清楚,但潜在的原因可能与吡哆醇缺乏症(磷酸吡哆醛是合成ALT和AST所必需的辅酶)[5-7]和/或尿毒症环境中存在抑制性物质有关[1]。

         

Subscribers log in here

To continue reading this article, you must log in with your personal, hospital, or group practice subscription. For more information or to purchase a personal subscription, click below on the option that best describes you:
Literature review current through: 2017-06 . | This topic last updated: 2016-01-15.
The content on the UpToDate website is not intended nor recommended as a substitute for medical advice, diagnosis, or treatment. Always seek the advice of your own physician or other qualified health care professional regarding any medical questions or conditions. The use of this website is governed by the UpToDate Terms of Use ©2017 UpToDate, Inc.
References
Top
  1. Cohen GA, Goffinet JA, Donabedian RK, Conn HO. Observations on decreased serum glutamic oxalacetic transaminase (SGOT) activity in azotemic patients. Ann Intern Med 1976; 84:275.
  2. Nanji AA. Decreased activity of commonly measured serum enzymes: causes and clinical significance. Am J Med Technol 1983; 49:241.
  3. Guh JY, Lai YH, Yang CY, et al. Impact of decreased serum transaminase levels on the evaluation of viral hepatitis in hemodialysis patients. Nephron 1995; 69:459.
  4. Fabrizi F, Lunghi G, Finazzi S, et al. Decreased serum aminotransferase activity in patients with chronic renal failure: impact on the detection of viral hepatitis. Am J Kidney Dis 2001; 38:1009.
  5. Wolf PL, Williams D, Coplon N, Coulson AS. Low aspartate transaminase activity in serum of patients undergoing chronic hemodialysis. Clin Chem 1972; 18:567.
  6. Hamfelt A. The effect of pyridoxal phosphate on the aminotransferase assay in blood. Scand J Clin Lab Invest Suppl 1966; 18:Suppl 92:181.
  7. Rej R, Fasce CF Jr, Vanderlinde RE. Increased aspartate aminotransferase activity of serum after in vitro supplementation with pyridoxal phosphate. Clin Chem 1973; 19:92.
  8. Fabrizi F, Lunghi G, Andrulli S, et al. Influence of hepatitis C virus (HCV) viraemia upon serum aminotransferase activity in chronic dialysis patients. Nephrol Dial Transplant 1997; 12:1394.
  9. Hung KY, Lee KC, Yen CJ, et al. Revised cutoff values of serum aminotransferase in detecting viral hepatitis among CAPD patients: experience from Taiwan, an endemic area for hepatitis B. Nephrol Dial Transplant 1997; 12:180.
  10. Espinosa M, Martin-Malo A, Alvarez de Lara MA, et al. High ALT levels predict viremia in anti-HCV-positive HD patients if a modified normal range of ALT is applied. Clin Nephrol 2000; 54:151.
  11. Fine A, McIntosh WB. Elevation of serum gamma-glutamyl transpeptidase in end-stage chronic renal failure. Scott Med J 1975; 20:113.
  12. Royse VL, Jensen DM, Corwin HL. Pancreatic enzymes in chronic renal failure. Arch Intern Med 1987; 147:537.
  13. Bastani B, Mifflin TE, Lovell MA, et al. Serum amylases in chronic and end-stage renal failure: effects of mode of therapy, race, diabetes and peritonitis. Am J Nephrol 1987; 7:292.
  14. Vaziri ND, Chang D, Malekpour A, Radaht S. Pancreatic enzymes in patients with end-stage renal disease maintained on hemodialysis. Am J Gastroenterol 1988; 83:410.
  15. Lin XZ, Chen TW, Wang SS, et al. Pancreatic enzymes in uremic patients with or without dialysis. Clin Biochem 1988; 21:189.
  16. Caruana RJ, Altman R, Fowler B, et al. Correlates of amylase and lipase levels in chronic dialysis patients. Int J Artif Organs 1988; 11:454.
  17. Kimmel PL, Tenner S, Habwe VQ, et al. Trypsinogen and other pancreatic enzymes in patients with renal disease: a comparison of high-efficiency hemodialysis and continuous ambulatory peritoneal dialysis. Pancreas 1995; 10:325.
  18. Shibasaki T, Matsuda H, Ohno I, et al. Significance of serum lipase in patients undergoing hemodialysis. Am J Nephrol 1996; 16:309.
  19. Masoero G, Bruno M, Gallo L, et al. Increased serum pancreatic enzymes in uremia: relation with treatment modality and pancreatic involvement. Pancreas 1996; 13:350.
  20. Collen MJ, Ansher AF, Chapman AB, et al. Serum amylase in patients with renal insufficiency and renal failure. Am J Gastroenterol 1990; 85:1377.
  21. Jiang CF, Ng KW, Tan SW, et al. Serum level of amylase and lipase in various stages of chronic renal insufficiency. Zhonghua Yi Xue Za Zhi (Taipei) 2002; 65:49.
  22. Robitaille R, Lafrance JP, Leblanc M. Altered laboratory findings associated with end-stage renal disease. Semin Dial 2006; 19:373.
  23. Schoenicke G, Grabensee B, Plum J. Dialysis with icodextrin interferes with measurement of serum alpha-amylase activity. Nephrol Dial Transplant 2002; 17:1988.
  24. Anderstam B, García-López E, Heimbürger O, Lindholm B. Determination of alpha-amylase activity in serum and dialysate from patients using icodextrin-based peritoneal dialysis fluid. Perit Dial Int 2003; 23:146.
  25. Montalto G, Soresi M, Carroccio A, et al. Influence of haemodialysis on lipase activity. Eur J Clin Chem Clin Biochem 1997; 35:237.