期刊
CLINICAL CHEMISTRY
卷 52, 期 6, 页码 1138-1143出版社
AMER ASSOC CLINICAL CHEMISTRY
DOI: 10.1373/clinchem.2005.064899
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Background: The reference intervals for hemoglobin A(1c) (Hb A(1c)) in pregnant women without diabetes are not well defined, and few examples of reference intervals established by networks of different laboratories are available. Methods: Five Italian Diabetic Care Units were involved in the study. Data were collected from 445 pregnant women without diabetes, selected on the basis of glucose challenge test results, and from 384 nonpregnant control women. The Hb A, measurements were performed with HPLC systems aligned to the Diabetes Control and Complications Trial, Plasma glucose measurements were also performed locally. Both Hb A,c and glucose measurements were harmonized by running appropriate external quality assessment schemes. The reference intervals were calculated in terms of nonparametric 2.5th to 97.5th percentiles with 0.90 confidence intervals. Results: The Hb A(1c) measurements were reproducible (CV = 2.0%) and accurate [mean (SE) difference from the target values, -0.10 (0.06)%]. Glucose measurements were also reproducible (mean CV = 3.2%) and accurate [difference from the target values, -0.01 (0.04) mmol/L]. To calculate common reference intervals, we merged the data collected in the different centers. The Hb A(1c) reference intervals were 4.0%-5.5% for pregnant nondiabetic women and 4.8%-6.2% for nonpregnant controls. Conclusions: Healthy pregnant women have lower Hb A, concentrations than nonpregnant women. The reference intervals for Hb A(1c) in pregnant women should therefore be lower than those currently in use. (c) 2006 American Association for Clinical Chemistry.
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