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本文引用的文献

1
Resting state hypothalamic response to glucose predicts glucose-induced attenuation in the ventral striatal response to food cues.静息状态下下丘脑对葡萄糖的反应可预测葡萄糖诱导的腹侧纹状体对食物线索反应的减弱。
Appetite. 2017 Sep 1;116:464-470. doi: 10.1016/j.appet.2017.05.038. Epub 2017 May 25.
2
Altered Brain Response to Drinking Glucose and Fructose in Obese Adolescents.肥胖青少年大脑对饮用葡萄糖和果糖的反应改变
Diabetes. 2016 Jul;65(7):1929-39. doi: 10.2337/db15-1216. Epub 2016 Apr 5.
3
Maternal obesity, gestational diabetes, breastfeeding and childhood overweight at age 2 years.母亲肥胖、妊娠期糖尿病、母乳喂养与2岁儿童超重
Pediatr Obes. 2017 Apr;12(2):171-178. doi: 10.1111/ijpo.12125. Epub 2016 Mar 8.
4
Gestational Diabetes Impairs Human Fetal Postprandial Brain Activity.妊娠期糖尿病会损害人类胎儿餐后大脑活动。
J Clin Endocrinol Metab. 2015 Nov;100(11):4029-36. doi: 10.1210/jc.2015-2692. Epub 2015 Oct 14.
5
Maternal adiposity negatively influences infant brain white matter development.母体肥胖对婴儿脑白质发育有负面影响。
Obesity (Silver Spring). 2015 May;23(5):1047-54. doi: 10.1002/oby.21055.
6
Automated removal of spurious intermediate cerebral blood flow volumes improves image quality among older patients: A clinical arterial spin labeling investigation.自动去除大脑中动脉血流伪影可改善老年患者的图像质量:一项临床动脉自旋标记研究。
J Magn Reson Imaging. 2015 Nov;42(5):1377-85. doi: 10.1002/jmri.24918. Epub 2015 Apr 15.
7
Association of maternal diabetes with autism in offspring.母亲糖尿病与后代自闭症的关联。
JAMA. 2015 Apr 14;313(14):1425-34. doi: 10.1001/jama.2015.2707.
8
Validity of self-assessment of pubertal maturation.青春期成熟自评的有效性。
Pediatrics. 2015 Jan;135(1):86-93. doi: 10.1542/peds.2014-0793. Epub 2014 Dec 22.
9
Maternal insulin sensitivity is associated with oral glucose-induced changes in fetal brain activity.母体胰岛素敏感性与口服葡萄糖引起的胎儿脑活动变化有关。
Diabetologia. 2014 Jun;57(6):1192-8. doi: 10.1007/s00125-014-3217-9. Epub 2014 Mar 28.
10
Gestational diabetes mellitus, maternal obesity, and adiposity in offspring.妊娠糖尿病、母体肥胖与子代肥胖
J Pediatr. 2014 Apr;164(4):807-10. doi: 10.1016/j.jpeds.2013.11.063. Epub 2013 Dec 31.

胎儿早期发育过程中暴露于母体肥胖或妊娠糖尿病环境下的儿童存在下丘脑改变,这些改变可预测未来体重增加。

Children Exposed to Maternal Obesity or Gestational Diabetes Mellitus During Early Fetal Development Have Hypothalamic Alterations That Predict Future Weight Gain.

机构信息

Division of Endocrinology, Department of Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA

Diabetes and Obesity Research Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA.

出版信息

Diabetes Care. 2019 Aug;42(8):1473-1480. doi: 10.2337/dc18-2581. Epub 2019 May 21.

DOI:10.2337/dc18-2581
PMID:31332028
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6647040/
Abstract

OBJECTIVE

Exposure in utero to maternal obesity or gestational diabetes mellitus (GDM) is linked to a high risk for obesity in offspring. Animal studies suggest that these exposures disrupt the development of the hypothalamus, a brain region that regulates body weight, predisposing offspring to develop obesity. This study tested the hypothesis in humans that in utero exposure to maternal obesity and/or GDM is associated with alterations in the hypothalamic response to glucose and the altered hypothalamic response would predict greater increases in child adiposity 1 year later.

RESEARCH DESIGN AND METHODS

Participants were 91 children aged 7-11 years with and without in utero exposure to GDM. Maternal prepregnancy BMI and GDM exposures were determined from electronic medical records. Arterial spin labeling MRI was used to determine the child's hypothalamic blood flow response to oral glucose. Anthropometric measures were acquired in all children at their initial visit and again 1 year later in a subset of 44 children.

RESULTS

Children exposed to GDM diagnosed at ≤26 weeks' gestation had increased hypothalamic blood flow (a marker of hypothalamic activation) in response to glucose when compared with unexposed children, and results remained after adjustments for child age, sex, BMI, and maternal prepregnancy BMI. Maternal prepregnancy BMI was positively associated with the child's hypothalamic response to glucose. Greater hypothalamic response to glucose predicted greater increases in child's BMI 1 year later.

CONCLUSIONS

Increased glucose-linked hypothalamic activation during childhood represents a possible mechanism by which exposure to maternal metabolic disorders during fetal development increases future risk for obesity.

摘要

目的

子宫内暴露于母体肥胖或妊娠糖尿病(GDM)与后代肥胖风险增加相关。动物研究表明,这些暴露会破坏下丘脑的发育,而下丘脑是调节体重的大脑区域,使后代易患肥胖症。本研究在人类中检验了这样一个假设,即子宫内暴露于母体肥胖和/或 GDM 与下丘脑对葡萄糖反应的改变有关,并且这种改变的下丘脑反应会预测孩子肥胖程度在 1 年后更大的增加。

研究设计和方法

参与者是 91 名年龄在 7-11 岁的儿童,他们在子宫内有或没有暴露于 GDM。通过电子病历确定母亲孕前 BMI 和 GDM 暴露情况。动脉自旋标记 MRI 用于确定孩子下丘脑对口服葡萄糖的血流反应。所有儿童在初次就诊时均进行了人体测量,其中 44 名儿童的一部分在 1 年后再次进行了测量。

结果

与未暴露的儿童相比,在妊娠 26 周前被诊断出患有 GDM 的儿童在接受葡萄糖刺激时下丘脑血流(下丘脑激活的标志物)增加,并且在调整了儿童年龄、性别、BMI 和母亲孕前 BMI 后,结果仍然存在。母亲孕前 BMI 与孩子对葡萄糖的下丘脑反应呈正相关。对葡萄糖的下丘脑反应越大,孩子的 BMI 在 1 年后增加的幅度越大。

结论

儿童时期与葡萄糖相关的下丘脑激活增加可能是胎儿发育过程中母体代谢紊乱暴露增加未来肥胖风险的一种机制。