Inflammation and Ovarian Function in Reproductive-Aged Women

IF 1.6 4区 医学 Q1 ANTHROPOLOGY American Journal of Human Biology Pub Date : 2024-12-02 DOI:10.1002/ajhb.24196
Anneliese Long, Anne Z. Steiner, Amanda L. Thompson, Hannah R. Jahnke, Benjamin S. Harris, Anne Marie Jukic
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Abstract

Introduction

Inflammation is a marker of immune activation. Inflammation may have an effect on both ovarian function and luteal function, both essential to pregnancy. High inflammation may also signal dysregulated processes within the ovary, which could be in part measured through Anti-Müllerian hormone, follicle-stimulating hormone, and inhibin B levels.

Objective

To determine the relationship between inflammation, measured by C-reactive protein, and three biomarkers of ovarian function during the early follicular phase: Anti-Müllerian hormone, follicle-stimulating hormone, and inhibin B.

Methods

Secondary cross-sectional analysis of data and serum obtained in Time to Conceive, a prospective cohort study sample of 843 women attempting pregnancy in central North Carolina from 2008 to 2016. Participants were aged 30 and 44 years, had no history of infertility, endometriosis, or polycystic ovarian syndrome, and were not currently breastfeeding. Serum samples were obtained on days 2, 3, or 4 of the menstrual cycle. C-reactive protein (natural-log transformed), Anti-Müllerian hormone (natural-log transformed), follicle-stimulating hormone (natural-log transformed), and inhibin B (untransformed) were measured in serum. Diminished ovarian reserve was examined dichotomously and defined as an Anti-Müllerian hormone level below 0.7 ng/mL.

Results

The analysis included 703 participants with C-reactive protein measured. In an adjusted linear regression model, a 20% increase in C-reactive protein was associated with a 0.57 pg/mL decrease in inhibin B (95% CI: −0.84 to −0.29 pg/mL) and a 0.535% decrease in follicle-stimulating hormone (95% CI: −1.01 to −0.06). Although there was not a significant relationship between Anti-Müllerian hormone and C-reactive protein, a 20% increase in C-reactive protein was associated with a 0.87% increase in Anti-Müllerian hormone (95% CI: −0.27 to 2.01). C-reactive protein was not associated with the odds of diminished ovarian reserve in an adjusted logistic regression model (OR: 0.97, 95% CI: 0.77–1.20).

Conclusions

Inflammation, as measured by C-reactive protein, is associated with early follicular phase follicle-stimulating hormone and inhibin B, although this is not true of AMH. Inflammation may exert an effect on ovarian function.

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育龄妇女的炎症与卵巢功能。
炎症是免疫激活的标志。炎症可能对卵巢功能和黄体功能都有影响,这两种功能对怀孕都很重要。高炎症也可能是卵巢内部失调的信号,这可以通过抗勒氏激素、促卵泡激素和抑制素B水平来部分测量。目的:确定c反应蛋白测量的炎症与卵泡早期卵巢功能的三种生物标志物:抗勒氏激素、促卵泡激素和抑制素b之间的关系。方法:对2008年至2016年北卡罗来纳州中部843名试图怀孕的女性的前瞻性队列研究样本《Time To pregnancy》中获得的数据和血清进行二次横断面分析。参与者年龄在30岁和44岁之间,没有不孕、子宫内膜异位症或多囊卵巢综合征的病史,目前没有母乳喂养。在月经周期的第2、3、4天采集血清样本。测定血清中的c反应蛋白(自然转化)、抗勒氏激素(自然转化)、促卵泡激素(自然转化)和抑制素B(未转化)。卵巢储备功能减退分为抗勒氏激素水平低于0.7 ng/mL。结果:分析包括703名参与者,测量c反应蛋白。在调整后的线性回归模型中,c反应蛋白增加20%与抑制素B降低0.57 pg/mL (95% CI: -0.84至-0.29 pg/mL)和促卵泡激素降低0.35% (95% CI: -1.01至-0.06)相关。虽然抗勒氏杆菌激素和c -反应蛋白之间没有显著关系,但c -反应蛋白增加20%与抗勒氏杆菌激素增加0.87%相关(95% CI: -0.27 ~ 2.01)。在调整后的logistic回归模型中,c反应蛋白与卵巢储备能力下降的几率无关(OR: 0.97, 95% CI: 0.77-1.20)。结论:炎症,如c反应蛋白测量,与卵泡期早期卵泡刺激素和抑制素B有关,尽管AMH并非如此。炎症可对卵巢功能产生影响。
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来源期刊
CiteScore
4.80
自引率
13.80%
发文量
124
审稿时长
4-8 weeks
期刊介绍: The American Journal of Human Biology is the Official Journal of the Human Biology Association. The American Journal of Human Biology is a bimonthly, peer-reviewed, internationally circulated journal that publishes reports of original research, theoretical articles and timely reviews, and brief communications in the interdisciplinary field of human biology. As the official journal of the Human Biology Association, the Journal also publishes abstracts of research presented at its annual scientific meeting and book reviews relevant to the field. The Journal seeks scholarly manuscripts that address all aspects of human biology, health, and disease, particularly those that stress comparative, developmental, ecological, or evolutionary perspectives. The transdisciplinary areas covered in the Journal include, but are not limited to, epidemiology, genetic variation, population biology and demography, physiology, anatomy, nutrition, growth and aging, physical performance, physical activity and fitness, ecology, and evolution, along with their interactions. The Journal publishes basic, applied, and methodologically oriented research from all areas, including measurement, analytical techniques and strategies, and computer applications in human biology. Like many other biologically oriented disciplines, the field of human biology has undergone considerable growth and diversification in recent years, and the expansion of the aims and scope of the Journal is a reflection of this growth and membership diversification. The Journal is committed to prompt review, and priority publication is given to manuscripts with novel or timely findings, and to manuscripts of unusual interest.
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