Serum insulin-like growth factor I reference values for an automated chemiluminescence immunoassay system:: Results from a multicenter study

被引:311
作者
Brabant, G
von zur Mühlen, A
Wüster, C
Ranke, MB
Kratzsch, J
Kiess, W
Ketelslegers, JM
Wilhelmsen, L
Hulthén, L
Saller, B
Mattsson, A
Wilde, J
Schemer, R
Kann, P
机构
[1] Hannover Med Sch, Dept Gastroenterol Hepatol & Endocrionol, DE-30625 Hannover, Germany
[2] Univ Med Clin, Dept Internal Med Endocrinol & Metab 1, Heidelberg, Germany
[3] Univ Tubingen, Childrens Hosp, Pediat Endocrinol Sect, Tubingen, Germany
[4] Univ Leipzig, Childrens Hosp, Leipzig, Germany
[5] Univ Leipzig, Inst Lab Med, Leipzig, Germany
[6] Univ Catholique Louvain, Sch Med, Dept Internal Med, B-1200 Brussels, Belgium
[7] Univ Gothenburg, Gothenburg, Sweden
[8] Pharmacia Corp, Erlangen, Germany
[9] Pharmacia Corp, Stockholm, Sweden
[10] Nichols Inst Diagnost, Bad Vilbel, Germany
[11] Univ Marburg, Dept Endocrinol & Diabet, Marburg, Germany
关键词
IGF-I; chemiluminesce assay; reference range; growth hormone;
D O I
10.1159/000071871
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Analysis of insulin-like growth factor I in serum (S-IGF-I) is an integral component in the diagnosis of GH-related disorders and is going to be of interest in the diagnosis and follow-up of many disorders. The objective of the present study was to develop cross-sectional reference values for S-IGF-I measured by an automated chemiluminescence immunoassay (Nichols Advantage(R)). Methods: The study included samples from 3,961 healthy subjects (2,201 males, 1,760 females) aged 1 month to 88 years. Six laboratories were involved in this study and the samples were analyzed by one of seven automated immunoassay systems run in these laboratories. For data analysis, polynomial age and sex-specific models were fitted after transformation of S-IGF-I values. Results: The results show the well-known age dependency of S-IGF-I levels. At ages <20, higher S-IGF-I levels were seen in girls with an estimated mean peak of 410 mug/l at age 14 and an estimated mean peak of 382 mug/l at age 16 in boys. Thereafter, a rapid decrease was seen to approximately 25 years of age, followed by a slow age-dependent decrease. In adulthood, S-IGF-I in males were slightly, but significantly higher than in females. It could be shown that the mean values of some reference sample subgroups differed significantly from the total mean. However, the multicenter approach used in this study reduces the impact of systematic population, sample handling and laboratory differences on the calculated reference mean. Conclusion: The present study establishes age- and sex-specific reference values for a fully automated immunoassay system based on a large population of healthy subjects. The established reference values may be used for this immunoassay system in different laboratories provided that the systematic difference between systems is low. Copyright (C) 2003 S. Karger AG, Basel.
引用
收藏
页码:53 / 60
页数:8
相关论文
共 23 条
  • [1] E2 supplementation selectively relieves GH's autonegative feedback on GH-releasing peptide-2-stimulated GH secretion
    Anderson, SM
    Wideman, L
    Patrie, JT
    Weltman, A
    Bowers, CY
    Veldhuis, JD
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (12) : 5904 - 5911
  • [2] Armitage P., 2002, STAT METHODS MED RES
  • [3] Attanasio A, 1998, J CLIN ENDOCR METAB, V83, P379
  • [4] BANG P, 1995, EUR J ENDOCRINOL, V132, P338
  • [5] Insulin-like growth factor-I: a key regulator of human cancer risk?
    Burroughs, KD
    Dunn, SE
    Barrett, JC
    Taylor, JA
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (07) : 579 - 581
  • [6] Plasma insulin-like growth factor I and prostate cancer risk: A prospective study
    Chan, JM
    Stampfer, MJ
    Giovannucci, E
    Gann, PH
    Ma, J
    Wilkinson, P
    Hennekens, CH
    Pollak, M
    [J]. SCIENCE, 1998, 279 (5350) : 563 - 566
  • [7] Evaluation of total IGF-I assay methods using samples from Type I and Type II diabetic patients
    Chestnut, RE
    Quarmby, V
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 2002, 259 (1-2) : 11 - 24
  • [8] Guidelines for optimizing growth hormone replacement therapy in adults
    de Boer, H
    van der Veen, E
    [J]. HORMONE RESEARCH, 1997, 48 : 21 - 30
  • [9] Optimizing GH therapy in adults and children
    Drake, WM
    Howell, SJ
    Monson, JP
    Shalet, SM
    [J]. ENDOCRINE REVIEWS, 2001, 22 (04) : 425 - 450
  • [10] General strategies to set quality specifications for reliability performance characteristics
    Fraser, CG
    [J]. SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1999, 59 (07) : 487 - 490