Dutta Anand, Saha Chandan, Johnson Cynthia S, Chalasani Naga
Division of Gastroenterology and Hepatology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Hepatology. 2009 Dec;50(6):1957-62. doi: 10.1002/hep.23200.
We conducted a study to characterize the variability in the upper limit of normal (ULN) for alanine aminotransferase (ALT) across different laboratories (labs) in Indiana and to understand factors leading to such variability. A survey was mailed to all eligible labs (n = 108) in Indiana, and the response rate was 62%. The survey queried for ALT ULN, the type of chemical analyzer used, five College of American Pathologists (CAP) sample results, and methods used to establish the reference interval. There was a wide variability in the ALT ULN for both men and women. Eighty-five percent of labs used chemical analyzers belonging to one of the four brands. For all five CAP samples, there was a statistically significant difference in ALT values measured by different analyzers (P < 0.0001), but these differences were not clinically significant. The majority of labs used the manufacturers' recommendations for establishing their ALT ULN rather than in-house healthy volunteer testing (only 17%). When healthy volunteers were tested, the process for testing was haphazard in terms of the number of individuals tested, frequency of testing, and criteria for choosing the reference population. After controlling for chemical analyzer type, there was no significant relationship between ALT ULN values and the method used for its establishment.
Wide variability in ALT ULN across different labs is more likely due to variable reference intervals of different chemical analyzers. It may be possible to minimize variability in ALT ULN by (1) each lab solely following the manufacturers' recommendations and (2) manufacturers of different analyzers following consistent and rigorous methodology in establishing the reference range. Alternatively, studies should be undertaken to identify outcome-based reference intervals for ALT.
我们开展了一项研究,以描述印第安纳州不同实验室中丙氨酸氨基转移酶(ALT)正常上限(ULN)的变异性,并了解导致这种变异性的因素。我们向印第安纳州所有符合条件的实验室(n = 108)邮寄了调查问卷,回复率为62%。该调查问卷询问了ALT ULN、所使用的化学分析仪类型、五个美国病理学家学会(CAP)样本的结果以及用于建立参考区间的方法。男性和女性的ALT ULN均存在很大变异性。85%的实验室使用了四个品牌之一的化学分析仪。对于所有五个CAP样本,不同分析仪测得的ALT值存在统计学显著差异(P < 0.0001),但这些差异无临床意义。大多数实验室使用制造商的建议来确定其ALT ULN,而非通过内部健康志愿者检测(仅17%)。在对健康志愿者进行检测时,检测过程在检测个体数量、检测频率和选择参考人群的标准方面都很随意。在控制化学分析仪类型后,ALT ULN值与其建立方法之间无显著关系。
不同实验室间ALT ULN的广泛变异性更可能是由于不同化学分析仪的参考区间不同。通过(1)每个实验室仅遵循制造商的建议以及(2)不同分析仪的制造商在建立参考范围时遵循一致且严格的方法,有可能使ALT ULN的变异性最小化。或者,应开展研究以确定基于结果的ALT参考区间。