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SERUM GLP-2 is Increased in Association with Excess Gestational Weight Gain.
Kahr, Maike K; Antony, Kathleen M; Galindo, Megan; Whitham, Megan; Hu, Min; Aagaard, Kjersti M; Suter, Melissa A.
Afiliación
  • Kahr MK; Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas.
  • Antony KM; Department of Obstetrics and Gynecology, University Hospital Zurich, Zurich, Switzerland.
  • Galindo M; Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas.
  • Whitham M; Department of Obstetrics and Gynecology, University of Wisconsin-Madison, Madison, Wisconsin.
  • Hu M; Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas.
  • Aagaard KM; Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas.
  • Suter MA; Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas.
Am J Perinatol ; 40(4): 400-406, 2023 03.
Article en En | MEDLINE | ID: mdl-33940644
OBJECTIVE: Obesity in pregnancy bears unique maternal and fetal risks. Obesity has also been associated with chronic inflammation, including elevated serum levels of interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α). Higher serum lipopolysaccharide (LPS) levels have been implicated in driving this inflammation, a phenomenon called metabolic endotoxemia (ME). GLP-2, a proglucagon-derived peptide, is believed to be integral in maintaining the integrity of the intestine in the face of LPS-mediated endotoxemia. We hypothesized that obesity and/or excess weight gain in pregnancy would be associated with an increase in maternal and neonatal markers of ME, as well as GLP-2. STUDY DESIGN: Paired maternal and neonatal (cord blood) serum samples (n = 159) were obtained from our pregnancy biobank repository. Serum levels of LPS, endotoxin core antibody-immunoglobulin M (EndoCAb-IgM), and GLP-2 were measured by ELISA. IL-6 and TNF-α were measured using a Milliplex assay. Results were stratified by maternal body mass index (BMI), maternal diabetes, and gestational weight gain (GWG). RESULTS: Maternal IL-6 is significantly decreased in the obese, diabetic cohort compared with the nonobese, nondiabetic cohorts (95.28 vs. 99.48 pg/mL, p = 0.047), whereas GLP-2 is significantly increased (1.92 vs. 2.89 ng/mL, p = 0.026). Neonatal TNF-α is significantly decreased in the obese cohort compared with the nonobese cohort (12.43 vs. 13.93 pg/mL, p = 0.044). Maternal GLP-2 is significantly increased in women with excess GWG compared with those with normal GWG (2.27 vs. 1.48 ng/mL, p = 0.014). We further found that neonatal IL-6 and TNF-α are negatively correlated with maternal BMI (-0.186, p = 0.036 and -0.179, p = 0.044, respectively) and that maternal and neonatal IL-6 showed a positive correlation (0.348, p < 0.001). CONCLUSION: Although we observed altered levels of markers of inflammation (IL-6 and TNF-α) with maternal obesity and diabetes, no changes in LPS or endoCAb-IgM were observed. We hypothesize that the increased GLP-2 levels in maternal serum in association with excess GWG may protect against ME in pregnancy. KEY POINTS: · Maternal serum levels of GLP-2, a proglucagon-derived peptide, are increased in obese, diabetic gravidae.. · Maternal serum GLP-2 levels are also increased in association with excess gestational weight gain compared with normal gestational weight gain.. · GLP-2 may be increased in association with obesity and weight gain to protect against metabolic endotoxemia in pregnancy..
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Endotoxemia / Ganancia de Peso Gestacional Tipo de estudio: Risk_factors_studies Límite: Female / Humans / Newborn / Pregnancy Idioma: En Revista: Am J Perinatol Año: 2023 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Endotoxemia / Ganancia de Peso Gestacional Tipo de estudio: Risk_factors_studies Límite: Female / Humans / Newborn / Pregnancy Idioma: En Revista: Am J Perinatol Año: 2023 Tipo del documento: Article Pais de publicación: Estados Unidos