Schrader H M, Jovanovic-Peterson L, Bevier W C, Peterson C M
Sansum Medical Research Foundation, Santa Barbara, CA 93105, USA.
Am J Perinatol. 1995 Jul;12(4):247-51. doi: 10.1055/s-2007-994465.
The purpose of this study was to modify the traditional gestational diabetes screening process in order to provide a test that might more reliably detect those women at risk of delivering a macrosomic infant despite a negative test for gestational diabetes mellitus (GDM). Pregnant women (n = 160) were screened for GDM at 24 to 28 weeks' gestation using the traditional 50 g glucose challenge test (GCT). In addition, glycosylated hemoglobin, glycosylated serum protein, and glycosylated plasma protein (GPP) were analyzed from blood drawn at this same time. If the patient's challenge test was positive (140 mg/dL or higher), a 100 g oral glucose tolerance test (OGTT) was performed. Twenty-three women had a positive GCT (14.4%) and five (3.13%) were excluded from further study because they received treatment for gestational diabetes based on a positive OGTT. None of the GCT-negative or the GCT-positive-OGTT-negative patients received treatment. Gestational age at delivery, infant gender, and birthweight were retrieved from birth records. Although several correlations with infant birthweight were found, the fasting plasma glucose (FPG) and GPPs proved most significant. The FPG on the OGTT significantly correlated with infant birthweight (p < 0.001; r = 0.94). A value greater than 90 mg/dL proved to be 100% sensitive and 64% specific for infant birthweight more than 4000 g. The relationship of the GPP and subsequent infant birthweight was also significant (p < 0.001; r = 0.81). A GPP greater than 23% proved to be 100% sensitive in predicting birthweight above 4000 g (11 of 11 infants); however, the test had a 52% specificity.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究的目的是改进传统的妊娠期糖尿病筛查流程,以便提供一种检测方法,能够更可靠地检测出那些尽管妊娠期糖尿病(GDM)检测结果为阴性,但仍有分娩巨大儿风险的女性。在妊娠24至28周时,使用传统的50克葡萄糖耐量试验(GCT)对160名孕妇进行GDM筛查。此外,同时采集的血液用于分析糖化血红蛋白、糖化血清蛋白和糖化血浆蛋白(GPP)。如果患者的耐糖试验呈阳性(140毫克/分升或更高),则进行100克口服葡萄糖耐量试验(OGTT)。23名女性GCT呈阳性(14.4%),5名(3.13%)因OGTT阳性而接受妊娠期糖尿病治疗,被排除在进一步研究之外。GCT阴性或GCT阳性-OGTT阴性的患者均未接受治疗。从出生记录中获取分娩时的孕周、婴儿性别和出生体重。尽管发现了一些与婴儿出生体重的相关性,但空腹血糖(FPG)和GPPs被证明最为显著。OGTT上的FPG与婴儿出生体重显著相关(p<0.001;r=0.94)。大于90毫克/分升的值对出生体重超过4000克的婴儿的敏感性为100%,特异性为64%。GPP与随后婴儿出生体重的关系也很显著(p<0.001;r=0.81)。GPP大于23%在预测出生体重高于4000克时的敏感性为100%(11名婴儿中的11名);然而,该检测的特异性为52%。(摘要截短至250字)