Estimation and application of biological variation of urinary δ-aminolevulinic acid and porphobilinogen in healthy individuals and in patients with acute intermittent porphyria

被引:53
作者
Aarsand, AK [1 ]
Petersen, PH
Sandberg, S
机构
[1] Haukeland Univ Hosp, Norwegian Porphyria Ctr, NAPOS, Biochim Clin Lab, NO-5021 Bergen, Norway
[2] Univ Bergen, Norwegian Qual Improvement Primary Care Labs, NOK LUS, Sect Gen Practice, Bergen, Norway
关键词
D O I
10.1373/clinchem.2005.060772
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Diagnosis of an attack of acute intermittent porphyria (AIP) is based on the demonstration of increased concentrations of porphobilinogen (PBG) and delta-aminolevulinic acid (ALA) in urine, but many All? patients also have high baseline concentrations in remission. The aim of this study was to estimate the biological variations of ALA, PBG, and porphyrins in healthy individuals and AIP patients to improve interpretation of test results. Methods: Fifteen healthy individuals and 15 AIP patients were included, and biological variations were calculated based on urine samples collected weekly for 10 consecutive weeks. For the All? patients, long-term variations were also estimated based on 7 samples collected through a 2-year period. Results: The porphyrin variances were inhomogeneously distributed; biological variations of porphyrins were therefore not calculated. The within-subject biological variations of ALA and PBG were 16%-20% in the short-term settings and for PBG, 25% in the long-term setting, giving reference change values of similar to 50% and 70%, respectively. The probability of detecting a 100% real change in PBG was 97% in the short-term setting and 80% in the long-term setting. Conclusions: In an All? patient, a 2-fold increase in PBG, independent of the baseline concentration, will be detected with a probability > 80% and is most likely related to the patient's disease and not caused only by analytical and biological variation. When PBG is used in the assessment of AIP-related symptoms, both the PBG concentration in remission and the length of time since the previous sample must be considered. (c) 2006 American Association for Clinical Chemistry.
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收藏
页码:650 / 656
页数:7
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