Employing fasting plasma glucose to safely limit the use of oral glucose tolerance tests in pregnancy: a pooled analysis of four Norwegian studies

被引:3
作者
Rai, Anam Shakil [1 ,2 ]
Sletner, Line [3 ]
Jenum, Anne Karen [4 ]
Overby, Nina Cecilie [2 ]
Stafne, Signe Nilssen [5 ,6 ]
Qvigstad, Elisabeth [7 ,8 ]
Pripp, Are Hugo [9 ]
Sagedal, Linda Reme [1 ,7 ,10 ]
机构
[1] Sorlandet Hosp, Dept Res, Kristiansand, Norway
[2] Univ Agder, Fac Hlth & Sport Sci, Dept Nutr & Publ Hlth, Kristiansand, Norway
[3] Akershus Univ Hosp, Dept Pediat & Adolescents Med, Akershus, Norway
[4] Univ Oslo, Inst Hlth & Soc, Dept Gen Med, Gen Practice Res Unit AFE, Oslo, Norway
[5] Norwegian Univ Sci & Technol NTNU, Dept Publ Hlth & Nursing, Trondheim, Norway
[6] Trondheim Reg & Univ Hosp, St Olavs Hosp, Dept Clin Serv, Trondheim, Norway
[7] Univ Oslo, Inst Clin Med, Oslo, Norway
[8] Oslo Univ Hosp, Dept Endocrinol Morbid Obes & Prevent Med, Oslo, Norway
[9] Oslo Univ Hosp, Oslo Ctr Biostat & Epidemiol Res Support Serv, Oslo, Norway
[10] Sorlandet Hosp, Dept Obstet & Gynaecol, Kristiansand, Norway
关键词
gestational diabetes; screening; pregnancy outcomes; fasting plasma glucose; OGTT; 3; GESTATIONAL DIABETES-MELLITUS; INTERNATIONAL ASSOCIATION; HYPERGLYCEMIA; POPULATION; GYNECOLOGY; OBSTETRICS; DIAGNOSIS; CRITERIA;
D O I
10.3389/fendo.2023.1278523
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/objective: There is no international consensus about the optimal approach to screening and diagnosis of gestational diabetes mellitus (GDM). Fasting plasma glucose (FPG) has been proposed as an alternative universal screening test to simplify the diagnosis of GDM. We investigate the ability of the FPG to predict a 2-hour glucose value below the cut-off for GDM, thereby "ruling out" the necessity of a full OGTT and assess the proportion of GDM-related complications associated with the identified FPG level.Materials and methods: This study included secondary data from four Norwegian pregnancy cohorts (2002-2013), encompassing 2960 women universally screened with late mid-pregnancy 75g OGTT measuring FPG and 2-hour glucose. For a range of FPG thresholds, we calculated sensitivity to predict elevated 2-hour glucose, number of OGTTs needed and percentage of GDM cases missed, applying modified World Health Organization (WHO) 2013 criteria ((WHO)-W-2013) and 2017 Norwegian criteria ((2017)Norwegian). We analyzed pregnancy outcomes for women above and below our selected threshold.Results: The prevalence of GDM was 16.6% ((WHO)-W-2013) and 10.1% ((2017)Norwegian). A FPG threshold of 4.7 mmol/L had a sensitivity of 76% ((WHO)-W-2013) and 80% ((2017)Norwegian) for detecting elevated 2-hour glucose, with few missed GDM cases (2.0% of those ruled out and 7.5% of all GDM cases for (WHO)-W-2013, and 1.1% of those ruled out and 7% of all GDM cases for (2017)Norwegian). When excluding women with FPG <4.7mmol/l and those with GDM based on FPG, only 24% ((WHO)-W-2013) and 29% ((2017)Norwegian) would require OGTT. Women with FPG <4.7mmol/l, including missed GDM cases, had low risk of large-for-gestational-age newborns, cesarean section and operative vaginal delivery.Conclusion: A FPG threshold of 4.7mmol/l as a first step when screening for GDM could potentially eliminate the need for OGTT in 70-77% of pregnancies. Women with FPG below this threshold appear to carry low risk of GDM-associated adverse pregnancy outcomes.
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页数:10
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