Within-subject biological variation in disease:: collated data and clinical consequences

被引:162
作者
Ricos, Carmen
Iglesias, Natalia
Garcia-Lario, Jose-Vicente
Simon, Margarita
Cava, Fernando
Hernandez, Amparo
Perich, Carmen
Minchinela, Joanna
Alvarez, Virtudes
Domenech, Maria-Vicenta
Jimenez, Carlos-Victor
Biosca, Carmen
Tena, Raquel
机构
[1] Univ Hosp, Clin Lab, Barcelona, Spain
[2] Hosp Motril, Serv Analisis Clin, Granada, Spain
[3] Lab Fdn Hosp Alcorcon, Madrid, Spain
[4] Lab Clin Hosp, Barcelona, Spain
[5] Lab Clin Bon Pastor, Barcelona, Spain
[6] Lab Clin Barcelones Nord, Barcelona, Spain
[7] Lab Clin Manso, Barcelona, Spain
[8] Hosp Germans Trias & Pujol, Serv Aanalisi Clin, Badalona, Spain
关键词
D O I
10.1258/000456307780945633
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
Quantitative data on the components of biological variation (BV) are used for several purposes, including calculating the reference change value (RCV) required for the assessment of the significance of changes in serial results in an individual. Pathology may modify the set point in diseased patients and, more importantly, the variation around that set-point. Our aim was to collate all published BV data in situations other than health. We report the within-subject coefficient of variation (CV,) for 66 quantities in 34 disease states. We compared the results with the CV, determined in healthy individuals and examined whether the data derived in specific diseases could be useful for clinical applications. For the majority of quantities studied, CV, values are of the same order in disease and health: thus the use of RCV derived from healthy subjects for monitoring patients would be reasonable. However, for a small number of quantities considered to be disease specific markers, the CV, differed from those in health. This could mean that RCV derived from healthy CV, may be inappropriate for monitoring patients in certain diseases. Hence, disease-specific RCVs may be clinically useful.
引用
收藏
页码:343 / 352
页数:10
相关论文
共 45 条
  • [1] Estimation and application of biological variation of urinary δ-aminolevulinic acid and porphobilinogen in healthy individuals and in patients with acute intermittent porphyria
    Aarsand, AK
    Petersen, PH
    Sandberg, S
    [J]. CLINICAL CHEMISTRY, 2006, 52 (04) : 650 - 656
  • [2] Components of biological variation of biochemical markers of bone turnover in Paget's bone disease
    Alvarez, L
    Ricós, C
    Peris, P
    Guañabens, N
    Monegal, A
    Pons, F
    Ballesta, AM
    [J]. BONE, 2000, 26 (06) : 571 - 576
  • [3] Are equally spaced specimen collections necessary to assess biological variation?: Evidence from renal transplant recipients
    Biosca, C
    Ricós, C
    Jiménez, CV
    Lauzurica, R
    Galimany, R
    [J]. CLINICA CHIMICA ACTA, 2000, 301 (1-2) : 79 - 85
  • [4] Biological variation at long-term renal post-transplantation
    Biosca, C
    Ricós, C
    Lauzurica, R
    Petersen, PH
    [J]. CLINICA CHIMICA ACTA, 2006, 368 (1-2) : 188 - 191
  • [5] Biosca C, 2001, CLIN CHEM, V47, P2146
  • [6] BROWNING MCK, 1988, CLIN CHEM, V34, P696
  • [7] BRUGUES JM, 1993, THESIS U BARCELONA
  • [8] High intraindividual variation of B-type natriuretic peptide (BNP) and amino-terminal proBNP in patients with stable chronic heart failure
    Bruins, S
    Fokkema, MR
    Römer, JWP
    DeJongste, MJL
    Van der Dijs, FPL
    Van den Ouewland, JMW
    Muskiet, FAJ
    [J]. CLINICAL CHEMISTRY, 2004, 50 (11) : 2052 - 2058
  • [9] ESCRICHE C, 1999, BIOL CLIN USEFULNESS, V1
  • [10] Fraser C.G, 2001, Biological variation: from principles to practice