气味和细胞因子:嗅觉和食物厌恶如何与怀孕早期的恶心和免疫调节有关。

IF 2.1 3区 医学 Q2 EVOLUTIONARY BIOLOGY
Evolution, Medicine, and Public Health Pub Date : 2025-09-24 eCollection Date: 2025-01-01 DOI:10.1093/emph/eoaf016
Dayoon Kwon, Daniel M T Fessler, Delaney A Knorr, Kyle S Wiley, Julie Sartori, David A Coall, Molly M Fox
{"title":"气味和细胞因子:嗅觉和食物厌恶如何与怀孕早期的恶心和免疫调节有关。","authors":"Dayoon Kwon, Daniel M T Fessler, Delaney A Knorr, Kyle S Wiley, Julie Sartori, David A Coall, Molly M Fox","doi":"10.1093/emph/eoaf016","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>During pregnancy, the maternal body undergoes extensive physiological adaptations to support embryonic growth, including whole-body remodeling, that may induce odor and food aversions, as well as nausea and vomiting. The biological mechanisms behind odor and food aversions, as well as nausea and vomiting in early pregnancy, remain largely unexplored. Our study investigated associations between these changes and cytokine profiles during pregnancy.</p><p><strong>Methodology: </strong>A cohort of pregnant Latina women in Southern California (<i>n</i> = 58) completed a structured questionnaire on pregnancy \"morning sickness\"-related symptoms and aversions. Maternal plasma cytokine levels were measured between 5 and 17 weeks' gestation.</p><p><strong>Results: </strong>About 64% of participants experienced odor or food aversions, primarily to tobacco smoke and meat; 67% reported nausea, and 66% experienced vomiting. Multivariable linear regression models revealed that odor aversions were associated with increased pro-inflammatory T-helper-cell type (Th) 1 composite cytokine levels. Women who found tobacco smoke aversive exhibited a shift toward Th1 immune responses, indicated by a higher Th1:Th2 ratio. Food aversions also showed a positive association with Th1 cytokine levels. A borderline positive association was noted between nausea and vomiting and the Th1:Th2 ratio.</p><p><strong>Conclusions: </strong>These findings are consistent with the hypothesis that gestational changes in olfactory and gustatory experience, and nausea and vomiting, reflect adaptive upregulation of behavioral prophylaxis in ways that could protect the fetus. If this elevated Th1:Th2 ratio and pro-inflammatory phenotype are part of the maternal and embryonic response to embryogenesis, the behavioral and biological markers that we explore may provide an accessible index of fetal development during early pregnancy.</p>","PeriodicalId":12156,"journal":{"name":"Evolution, Medicine, and Public Health","volume":"13 1","pages":"269-280"},"PeriodicalIF":2.1000,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12476167/pdf/","citationCount":"0","resultStr":"{\"title\":\"Of scents and cytokines: How olfactory and food aversions relate to nausea and immunomodulation in early pregnancy.\",\"authors\":\"Dayoon Kwon, Daniel M T Fessler, Delaney A Knorr, Kyle S Wiley, Julie Sartori, David A Coall, Molly M Fox\",\"doi\":\"10.1093/emph/eoaf016\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>During pregnancy, the maternal body undergoes extensive physiological adaptations to support embryonic growth, including whole-body remodeling, that may induce odor and food aversions, as well as nausea and vomiting. The biological mechanisms behind odor and food aversions, as well as nausea and vomiting in early pregnancy, remain largely unexplored. Our study investigated associations between these changes and cytokine profiles during pregnancy.</p><p><strong>Methodology: </strong>A cohort of pregnant Latina women in Southern California (<i>n</i> = 58) completed a structured questionnaire on pregnancy \\\"morning sickness\\\"-related symptoms and aversions. Maternal plasma cytokine levels were measured between 5 and 17 weeks' gestation.</p><p><strong>Results: </strong>About 64% of participants experienced odor or food aversions, primarily to tobacco smoke and meat; 67% reported nausea, and 66% experienced vomiting. Multivariable linear regression models revealed that odor aversions were associated with increased pro-inflammatory T-helper-cell type (Th) 1 composite cytokine levels. Women who found tobacco smoke aversive exhibited a shift toward Th1 immune responses, indicated by a higher Th1:Th2 ratio. Food aversions also showed a positive association with Th1 cytokine levels. A borderline positive association was noted between nausea and vomiting and the Th1:Th2 ratio.</p><p><strong>Conclusions: </strong>These findings are consistent with the hypothesis that gestational changes in olfactory and gustatory experience, and nausea and vomiting, reflect adaptive upregulation of behavioral prophylaxis in ways that could protect the fetus. If this elevated Th1:Th2 ratio and pro-inflammatory phenotype are part of the maternal and embryonic response to embryogenesis, the behavioral and biological markers that we explore may provide an accessible index of fetal development during early pregnancy.</p>\",\"PeriodicalId\":12156,\"journal\":{\"name\":\"Evolution, Medicine, and Public Health\",\"volume\":\"13 1\",\"pages\":\"269-280\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-09-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12476167/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Evolution, Medicine, and Public Health\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1093/emph/eoaf016\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"EVOLUTIONARY BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Evolution, Medicine, and Public Health","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/emph/eoaf016","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"EVOLUTIONARY BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景:在怀孕期间,母体经历了广泛的生理适应以支持胚胎生长,包括全身重塑,这可能引起气味和食物厌恶,以及恶心和呕吐。气味和食物厌恶,以及怀孕早期的恶心和呕吐背后的生物学机制,在很大程度上仍未被探索。我们的研究调查了这些变化与怀孕期间细胞因子谱之间的关系。方法:南加州的一组拉丁裔孕妇(n = 58)完成了一份关于妊娠“晨吐”相关症状和厌恶的结构化问卷。在妊娠5 ~ 17周期间测定母体血浆细胞因子水平。结果:大约64%的参与者经历了气味或食物厌恶,主要是烟草烟雾和肉类;67%的人恶心,66%的人呕吐。多变量线性回归模型显示,气味厌恶与促炎t -辅助细胞型(Th) 1复合细胞因子水平升高有关。发现烟草烟雾厌恶的女性表现出向Th1免疫反应的转变,表明Th1:Th2比率较高。对食物的厌恶也与Th1细胞因子水平呈正相关。恶心和呕吐与Th1:Th2比值呈边缘性正相关。结论:这些发现与假设一致,即妊娠期嗅觉和味觉体验以及恶心和呕吐的变化反映了行为预防的适应性上调,从而可以保护胎儿。如果这种升高的Th1:Th2比率和促炎表型是母体和胚胎对胚胎发生的反应的一部分,那么我们探索的行为和生物学标记可能为妊娠早期胎儿发育提供一个可访问的指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Of scents and cytokines: How olfactory and food aversions relate to nausea and immunomodulation in early pregnancy.

Of scents and cytokines: How olfactory and food aversions relate to nausea and immunomodulation in early pregnancy.

Of scents and cytokines: How olfactory and food aversions relate to nausea and immunomodulation in early pregnancy.

Of scents and cytokines: How olfactory and food aversions relate to nausea and immunomodulation in early pregnancy.

Background: During pregnancy, the maternal body undergoes extensive physiological adaptations to support embryonic growth, including whole-body remodeling, that may induce odor and food aversions, as well as nausea and vomiting. The biological mechanisms behind odor and food aversions, as well as nausea and vomiting in early pregnancy, remain largely unexplored. Our study investigated associations between these changes and cytokine profiles during pregnancy.

Methodology: A cohort of pregnant Latina women in Southern California (n = 58) completed a structured questionnaire on pregnancy "morning sickness"-related symptoms and aversions. Maternal plasma cytokine levels were measured between 5 and 17 weeks' gestation.

Results: About 64% of participants experienced odor or food aversions, primarily to tobacco smoke and meat; 67% reported nausea, and 66% experienced vomiting. Multivariable linear regression models revealed that odor aversions were associated with increased pro-inflammatory T-helper-cell type (Th) 1 composite cytokine levels. Women who found tobacco smoke aversive exhibited a shift toward Th1 immune responses, indicated by a higher Th1:Th2 ratio. Food aversions also showed a positive association with Th1 cytokine levels. A borderline positive association was noted between nausea and vomiting and the Th1:Th2 ratio.

Conclusions: These findings are consistent with the hypothesis that gestational changes in olfactory and gustatory experience, and nausea and vomiting, reflect adaptive upregulation of behavioral prophylaxis in ways that could protect the fetus. If this elevated Th1:Th2 ratio and pro-inflammatory phenotype are part of the maternal and embryonic response to embryogenesis, the behavioral and biological markers that we explore may provide an accessible index of fetal development during early pregnancy.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Evolution, Medicine, and Public Health
Evolution, Medicine, and Public Health Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
5.40
自引率
2.70%
发文量
37
审稿时长
8 weeks
期刊介绍: About the Journal Founded by Stephen Stearns in 2013, Evolution, Medicine, and Public Health is an open access journal that publishes original, rigorous applications of evolutionary science to issues in medicine and public health. It aims to connect evolutionary biology with the health sciences to produce insights that may reduce suffering and save lives. Because evolutionary biology is a basic science that reaches across many disciplines, this journal is open to contributions on a broad range of topics.
×
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:604180095
Book学术官方微信