Longitudinal changes in leptin and adiponectin concentrations through uncomplicated pregnancy

IF 0.1 Q4 OTORHINOLARYNGOLOGY
Marina Pijanović, A. Stefanović, M. Miljkovic, Snežana Marić-Krejović, S. Spasić
{"title":"Longitudinal changes in leptin and adiponectin concentrations through uncomplicated pregnancy","authors":"Marina Pijanović, A. Stefanović, M. Miljkovic, Snežana Marić-Krejović, S. Spasić","doi":"10.1515/labmed-2017-0052","DOIUrl":null,"url":null,"abstract":"Abstract Background: Leptin and adiponectin play an important role during normal gestation; they are implicated in energy metabolism, glucose utilization and inflammation. Osteocalcin is released into circulation during bone formation; it also affects glucose metabolism by regulating insulin secretion and sensitivity, possibly mediated by adiponectin. The aim of this study was to explore the longitudinal changes of leptin and adiponectin in pregnancy, and their associations with lipid profile, insulin and bone formation parameters in late pregnancy. Methods: Leptin, adiponectin, lipid status parameters, C-reactive protein (CRP), insulin, 25-hydroxyvitamin D, osteocalcin and procollagen type 1 aminoterminal propeptide (P1NP) were measured in the sera of 38 healthy pregnant women. The samples were obtained in the 1st, 2nd, early and late 3rd trimester, and post-partum. Results: Leptin was significantly increased in the 3rd trimester. The decrease of adiponectin was significant only in postpartum. Osteocalcin and P1NP increased in the late 3rd trimester and postpartum. Leptin was significantly positively correlated with body mass index (BMI), uric acid, insulin, osteocalcin, P1NP and CRP in the 3rd trimester; adiponectin was positively correlated with high-density lipoprotein (HDL) cholesterol, and negatively with BMI, glucose, osteocalcin, triglycerides and insulin. Multiple regression analysis showed that only HDL is independently associated with adiponectin. Conclusions: The results of our study suggest complex interactions of leptin and adiponectin with glucose, lipid and bone metabolism during pregnancy. Adiponectin might be part of the protective systems that counterbalance a transient proatherogenic state observed in pregnancy mainly by improving the HDL levels. The exact mechanisms and potential implications in pathological states of pregnancy remain unexplained and require further investigation.","PeriodicalId":49926,"journal":{"name":"Laboratoriumsmedizin-Journal of Laboratory Medicine","volume":"1 1","pages":"129 - 136"},"PeriodicalIF":0.1000,"publicationDate":"2017-07-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Laboratoriumsmedizin-Journal of Laboratory Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/labmed-2017-0052","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"OTORHINOLARYNGOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Abstract Background: Leptin and adiponectin play an important role during normal gestation; they are implicated in energy metabolism, glucose utilization and inflammation. Osteocalcin is released into circulation during bone formation; it also affects glucose metabolism by regulating insulin secretion and sensitivity, possibly mediated by adiponectin. The aim of this study was to explore the longitudinal changes of leptin and adiponectin in pregnancy, and their associations with lipid profile, insulin and bone formation parameters in late pregnancy. Methods: Leptin, adiponectin, lipid status parameters, C-reactive protein (CRP), insulin, 25-hydroxyvitamin D, osteocalcin and procollagen type 1 aminoterminal propeptide (P1NP) were measured in the sera of 38 healthy pregnant women. The samples were obtained in the 1st, 2nd, early and late 3rd trimester, and post-partum. Results: Leptin was significantly increased in the 3rd trimester. The decrease of adiponectin was significant only in postpartum. Osteocalcin and P1NP increased in the late 3rd trimester and postpartum. Leptin was significantly positively correlated with body mass index (BMI), uric acid, insulin, osteocalcin, P1NP and CRP in the 3rd trimester; adiponectin was positively correlated with high-density lipoprotein (HDL) cholesterol, and negatively with BMI, glucose, osteocalcin, triglycerides and insulin. Multiple regression analysis showed that only HDL is independently associated with adiponectin. Conclusions: The results of our study suggest complex interactions of leptin and adiponectin with glucose, lipid and bone metabolism during pregnancy. Adiponectin might be part of the protective systems that counterbalance a transient proatherogenic state observed in pregnancy mainly by improving the HDL levels. The exact mechanisms and potential implications in pathological states of pregnancy remain unexplained and require further investigation.
无并发症妊娠期间瘦素和脂联素浓度的纵向变化
背景:瘦素和脂联素在正常妊娠中起重要作用;它们与能量代谢、葡萄糖利用和炎症有关。骨钙素在骨形成过程中被释放到循环中;它还通过调节胰岛素分泌和敏感性影响葡萄糖代谢,可能由脂联素介导。本研究旨在探讨妊娠期瘦素和脂联素的纵向变化及其与妊娠后期血脂、胰岛素和骨形成参数的关系。方法:测定38例健康孕妇血清中瘦素、脂联素、脂质状态参数、c反应蛋白(CRP)、胰岛素、25-羟基维生素D、骨钙素、前胶原1型氨基末端前肽(P1NP)水平。样本采集于妊娠1、2、3月早期和晚期以及产后。结果:瘦素在妊娠晚期明显升高。脂联素的下降仅在产后有显著性意义。骨钙素和P1NP在妊娠晚期和产后升高。妊娠晚期瘦素与体重指数(BMI)、尿酸、胰岛素、骨钙素、P1NP、CRP呈显著正相关;脂联素与高密度脂蛋白(HDL)胆固醇呈正相关,与BMI、葡萄糖、骨钙素、甘油三酯、胰岛素呈负相关。多元回归分析表明,只有HDL与脂联素独立相关。结论:我们的研究结果提示瘦素和脂联素与妊娠期间葡萄糖、脂质和骨代谢的复杂相互作用。脂联素可能是保护系统的一部分,主要通过改善高密度脂蛋白水平来平衡怀孕期间观察到的短暂的动脉粥样硬化状态。妊娠病理状态的确切机制和潜在影响仍未解释,需要进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
0.80
自引率
0.00%
发文量
1
审稿时长
>12 weeks
期刊介绍: Information not localized
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信