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The correlation of adipocyte fatty acid binding protein and leptin in umbilical cord blood with non-GDM macrosomia |
YE Yan1, DING Miaomiao1, WANG Yuhuan2, YAN Hongtao1, YANG Xinjun1 |
1.Department of Preventive Medicine, School of Public Health and Management, Wenzhou Medical University, Wenzhou 325035, China; 2.Department of Obstetrics, the Second Affiliated Hospital & Yuying Children’s Hospital of Wenzhou Medical University, Wenzhou 325027, China |
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Cite this article: |
YE Yan,DING Miaomiao,WANG Yuhuan, et al. The correlation of adipocyte fatty acid binding protein and leptin in umbilical cord blood with non-GDM macrosomia[J]. JOURNAL OF WEZHOU MEDICAL UNIVERSITY, 2020, 50(9): 700-704.
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Abstract Objective: To investigate the correlation of AFABP and leptin in umbilical cord blood with non-GDM macrosomia. Methods: A case-control study was performed. Newborns were selected, with 46 macrosomia and 46 normal-birth-weight, in the Obstetric Department of the Second Affiliated Hospital & Yuying Children’s Hospital of Wenzhou Medical University. A self-designed questionnaire was used to collect maternal and fetal baseline information. The umbilical cord blood concentration of AFABP and leptin was measured by ELISA and RIA, respectively. Logistic regression analysis was used to analyze the influencing factors of non-GDM macrosomia. Results: There was no difference in cord blood AFABP concentration between the two groups, and the leptin concentration in macrosomia cord blood was significantly higher than that of control group (P<0.05). Stratified analysis found that in the higher gestational layer (gestational age>39) and excessive gestational weight gain layer, AFABP concentration in macrosomia cord blood was significantly lower than that of the control group (P<0.05); the leptin concentration in macrosomia cord blood was significantly higher than that of the control group in the male fetal layer, lower gestational age layer (gestational age≤39) and normal gestational weight gain layer(P<0.05). Multivariable logistic regression analysis showed that the lower AFABP concentration in umbilical cord blood could increase the risk of non-GDM macrosomia (OR=3.792, 95%CI: 1.266~11.359, P<0.05), the occurrence of non-GDM macrosomia was also influenced by fetal gender, gestational age and gestational weight gain. Conclusion: Lower AFABP concentration in umbilical cord blood may increase the risk of non-GDM macrosomia. Further studies are required to elucidate its molecular mechanism.
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Received: 30 April 2020
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[1] JUNIOR E A, PEIXOTO A B, ZAMARIAN A C, et al. Macrosomia[J]. Best Pract Res Clin Obstet Gynaecol, 2017, 38: 83-96.
[2] USTA A, USTA C S, YILDIZ A, et al. Frequency of fetal macrosomia and the associated risk factors in pregnancies without gestational diabetes mellitus[J]. Pan Afr Med J, 2017, 26: 62.
[3] 万里, 朱萍, 潘熊飞. 巨大儿对母婴健康不良影响的研究进展[J]. 中国计划生育和妇产科, 2018, 10(5): 33-37.
[4] TROJNAR M, PATRO-MALYSZA J, KIMBER-TROJNAR Z, et al. Associations between fatty acid-binding protein 4-A proinflammatory adipokine and insulin resistance, gestational and type 2 diabetes mellitus[J]. Cells, 2019, 8(3): 227.
[5] EBERT T, GEBHARDT C, SCHOLZ M, et al. Relationship between 12 adipocytokines and distinct components of the metabolic syndrome[J]. J Clin Endocrinol Metab, 2018, 103(3): 1015-1023.
[6] BOYLE C N, LE FOLL C. Amylin and leptin interaction: Role during pregnancy, lactation and neonatal development [J]. Neuroscience, 2020. DOI: 10.1016/j.neuroscience.2019. 11.034.
[7] UYSAL K T, SCHEJA L, WIESBROCK S M, et al. Improved glucose and lipid metabolism in genetically obese mice lacking aP2[J]. Endocrinology, 2000, 141(9): 3388-3396.
[8] Instiute of Medicine (US) and National Research Council (US) Committee to Reexamine IOM Pregnancy Weight Guidelines, RASMUSSEN K M, YAKTINE A L. Weight gain during pregnancy: reexamining the guidelines[M]. Washington DC: The National Academies Press, 2009.
[9] PAPATHANASIOU A E, BRIANA D D, GAVRILI S, et al. Cord blood fatty acid-binding protein-4 levels are upregulated at both ends of the birthweight spectrum[J]. Acta Paediatr, 2019, 108(11): 2083-2088.
[10] SIAHANIDOU T, MARGELI A, DAVRADOU M, et al. Circulating adipocyte fatty acid binding protein levels in healthy preterm infants: Positive correlation with weight gain and total-cholesterol levels[J]. Early Hum Dev, 2010, 86(4): 197-201.
[11] HOU R L, JIN W Y, CHEN X Y, et al. Cord blood C-peptide, insulin, HbA1c, and lipids levels in small-and large-for-gestational-age newborns[J]. Med Sci Monit, 2014, 20: 2097-2105.
[12] PATRO-MALYSZE J, TROJNAR M, KIMBER-TROJNAR Z, et al. FABP4 in gestational diabetes-association between mothers and offspring[J]. J Clin Med, 2019, 8(3): 285.
[13] ORTEGA-SENOVILLA H, SCHAEFER-GRAF U, MEITZNER K, et al. Gestational diabetes mellitus causes changes in the concentrations of adipocyte fatty acid binding protein and other adipocytokines in cord blood[J]. Diabetes Care, 2011, 34(9): 2061-2066.
[14] GHADGE A A, KHAIRE A A. Leptin as a predictive marker for metabolic syndrome[J]. Cytokine, 2019, 121: 154735.
[15] CHAOIMH C N, MURRAY D M, KENNY L C, et al. Cord blood leptin and gains in body weight and fat mass during infancy[J]. Eur J Endocrinol, 2016, 175(5): 403-410.
[16] ZAREAAN E, HEIDARPOUR M, KARGARZADEH E, et al. Association of maternal and umbilical cord blood leptin concentrations and abnormal color Doppler indices of umbilical artery with fetal growth restriction[J]. Int J Reprod Biomed, 2017, 15(3): 135-140.
[17] BUCUR-GROSU M L, AVASILOAIEI A, MOSCALU M, et al. Desacylated ghrelin and leptin in the cord blood of small-forgestational-age newborns with intrauterine growth restriction[J]. Acta Endocrinol (Buchar), 2019, 15(3): 305-310.
[18] VINTURACHE A E, CHAPUT K H, TOUGH S C. Pre-pregnancy body mass index (BMI) and macrosomia in a canadian birth cohort[J]. J Matern Fetal Neonatal Med, 2017, 30(1): 109-116.
[19] HUA X G, JIANG W, HU R, et al. Large for gestational age and macrosomia in pregnancies without gestational diabetes mellitus[J]. J Matern Fetal Neonatal Med, 2020, 33(21): 3549-3558.
[20] DOU H X, WAND T, SU H X, et al. Exogenous FABP4 interferes with differentiation, promotes lipolysis and inflammation in adipocytes[J]. Endocrine, 2020, 67(3): 587-596.
[21] HOFER P, BOESZOERMENYI A, JAEGER D, et al. Fatty Acid-binding proteins interact with comparative gene identification-58 linking lipolysis with lipid ligand shuttling [J]. J Biol Chem, 2015, 290(30): 18438-18453. |
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