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First-trimester fasting plasma glucose as a predictor of subsequent gestational diabetes mellitus and adverse fetomaternal outcomes: A systematic review and meta-analysis. | LitMetric

AI Article Synopsis

  • The study aimed to assess whether elevated fasting plasma glucose (FPG) levels in the first trimester can predict the development of gestational diabetes mellitus (GDM) later in pregnancy, as well as associated adverse events.
  • It analyzed data from 16 studies involving over 115,000 pregnancies and found that FPG levels above 5.1 mmol/L (92 mg/dL) significantly increased the risk of GDM and several pregnancy complications including pre-eclampsia and large-for-gestational-age infants.
  • However, the research had limitations, such as a lack of diverse studies reporting on higher FPG thresholds, particularly at 6.1 mmol/L (110 mg/dL).

Article Abstract

Background: The implication of intermediately elevated fasting plasma glucose (FPG) in the first trimester of pregnancy is uncertain.

Purpose: The primary outcome of the meta-analysis was to analyze if intermediately elevated first-trimester FPG could predict development of GDM at 24-28 weeks. The secondary outcomes were to determine if the commonly used FPG cut-offs 5.1 mmol/L (92 mg/dL), 5.6 mmol/L (100 mg/dL), and 6.1 mmol/L (110 mg/dL) correlated with adverse pregnancy events.

Data Sources: Databases were searched for articles published from 2010 onwards for studies examining the relationship between first-trimester FPG and adverse fetomaternal outcomes.

Study Selection: A total of sixteen studies involving 115,899 pregnancies satisfied the inclusion criteria.

Data Extraction And Data Synthesis: Women who developed GDM had a significantly higher first-trimester FPG than those who did not [MD 0.29 mmoL/l (5 mg/dL); 95 % CI: 0.21-0.38; P < 0.00001]. First-trimester FPG ≥5.1 mmol/L (92 mg/dL) predicted the development of GDM at 24-28 weeks [RR 3.93 (95 % CI: 2.67-5.77); P < 0.0000], pre-eclampsia [RR 1.55 (95%CI:1.14-2.12); P = 0.006], gestational hypertension [RR1.47 (95%CI:1.20-1.79); P = 0.0001], large-for-gestational-age (LGA) [RR 1.32 (95%CI:1.13-1.54); P = 0.0004], and macrosomia [RR1.29 (95%CI:1.15-1.44); P < 0.001]. However, at the above threshold, the rates of preterm delivery, lower-segment cesarean section (LSCS), small-for gestational age (SGA), and neonatal hypoglycemia were not significantly higher. First-trimester FPG ≥5.6 mmol/L (100 mg/dL) correlated with occurrence of macrosomia [RR1.47 (95 % CI:1.22-1.79); P < 0.0001], LGA [RR 1.43 (95%CI:1.24-1.65); P < 0.00001], and preterm delivery [RR1.51 (95%CI:1.15-1.98); P = 0.003], but not SGA and LSCS.

Limitations: Only one study reported outcomes at first-trimester FPG of 6.1 mmol/L (110 mg/dL), and hence was not analyzed.

Conclusion: The risk of development of GDM at 24-28 weeks increased linearly with higher first-trimester FPG. First trimester FPG cut-offs of 5.1 mmol/L (92 mg/dL) and 5.6 mmol/L (100 mg/dL) predicted several adverse pregnancy outcomes.

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Source
http://dx.doi.org/10.1016/j.dsx.2024.103051DOI Listing

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