Evaluating the intersection between sexually transmitted infections, inflammation and reproductive success
Evaluating the intersection between sexually transmitted infections, inflammation and reproductive success
批准号:
10115581
负责人:
Brandie DePaoli Taylor
金额:
$10.94万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-03-01 至 2021-06-30
关键词:
AddressAdverse eventAgeAnti-Inflammatory AgentsAspirinBiological AssayBirthBirth RateBloodBlood PlateletsC-reactive proteinCellsChlamydiaChlamydia trachomatisChronicCicatrixClinicalConceptionsCouplesDataDecidual Cell ReactionsDefectDiagnosisDiagnosticDiseaseDoseEndometrialEpigenetic ProcessEpithelial CellsEventExposure toFamilyFertilityFrequenciesFundingFutureGoalsGrowthHigh PrevalenceIL6 geneIL8 geneImmuneImmune signalingImmunologic ReceptorsInfectionInfertilityInflammationInterleukin-15LaboratoriesLeadLegal patentLinkLive BirthMeasurementMeasuresMediatingMenstrual cycleMetadataMethodsMissionMorbidity - disease rateMycoplasmaMycoplasma genitaliumNatural ImmunityNatureNeisseria gonorrhoeaeOutcomePGF genePTGS2 genePathogenesisPathologyPathway interactionsPhenotypePlacebosPlacentationPlasmaPopulationPregnancyPregnancy HistoriesPregnancy lossPrevalencePreventionProstaglandinsPublic HealthRandomizedRecording of previous eventsReproductionReproductive HealthReproductive MedicineResearchResearch SupportRiskRouteSTI preventionSerologySeroprevalencesSerumServicesSexually Transmitted DiseasesSterilityStimulusSubfecunditySurveysTarget PopulationsThromboxane A2TimeTissuesTrainingTrichomonas vaginalisTubeUnited States National Institutes of HealthVariantVascular Endothelial Growth FactorsWomanWomen&aposs GroupWorkadverse event riskadverse outcomeangiogenesiscytokineearly pregnancy lossfetalhigh riskhigh risk populationhistone modificationhuman diseaseimprovedimproved outcomeinflammatory markerinnovationinsightinterestmemberobstetric carepathogenreproductivereproductive morbidityreproductive outcomereproductive successreproductive tractseropositivesubfertilitytime-to-pregnancytissue repairtrying to conceivetubal infertilityyoung adult
中文摘要
项目摘要
约20%的临床确认妊娠的女性发生妊娠丢失。有过
流产代表了那些试图怀孕的人的很大一部分,但治疗仅限于广泛的
无法获得生育服务。阿司匹林对妊娠和生殖的影响(EAGeR)试验的数据
表明孕前低剂量阿司匹林治疗会增加有妊娠史妇女的出生率
当存在由C-反应蛋白确定的孕前慢性低度炎症时损失。有
迫切需要了解导致孕前慢性低度炎症的途径。这将
帮助确定更广泛的妇女群体,他们将受益于阿司匹林治疗,并告知阿司匹林的使用
在生殖医学方面。我们假设,先前暴露于常见的性传播感染(STI)
会导致长期免疫失调和组织修复缺陷。在那些有过
妊娠丢失,STI血清学可能表明随后发生不良事件的风险或代表一组女性
能从孕前抗炎治疗中获益流行且大多无症状的性传播感染,
因为沙眼衣原体和生殖支原体可以上升到上生殖道,
炎症、组织损伤和瘢痕形成。不幸的是,大多数女性在年轻时获得这些性传播感染,
他们不知道自己曾经被感染过。“训练的先天免疫”的概念假定先天免疫细胞
在通过表观遗传诱导的感染刺激后,
免疫细胞和上皮细胞的变化。事实上,这些性传播感染与输卵管不孕有关,但与
生殖力受损的其他措施是有限的。本提案的具体目标是:1)确定
沙眼衣原体和生殖支原体血清阳性影响妊娠时间,
有流产史的妇女的流产率和出生率,同时调整已知感染的其他性传播感染,
上生殖道2)确定STI血清阳性女性是否具有独特的血液免疫和血管生成特征
与血清反应阴性的女性相比。3)确定既往随机接受阿司匹林治疗的STI血清阳性女性
作为EAGeR试验的一部分的治疗(上述结果)改善了分娩结局。本研究将
包括来自EAGeR试验的1078名女性。所有妇女都有流产史,但没有不孕症史。
从极其详细的生殖结果研究中获得孕前数据是独一无二的。此外,本发明还
我们的团队包括STI诊断领域的世界领先者,可进行可靠的血清学测量。我们将
我还利用我们团队成员的专业知识,目前资助开发方法,以解决
推广性,将我们的结果传达给有流产史的美国女性目标人群
全国家庭成长调查。鉴于美国和欧洲的性传播感染患病率大幅上升,
流产的频率,这项研究和我们未来的工作可能会影响大量的妇女。
英文摘要
PROJECT SUMMARY ABSTRACT
Pregnancy loss occurs in ~20% of women with a clinically recognized pregnancy. Couples with histories of
pregnancy loss represent a large portion of those trying to conceive, but treatment is limited to widely
inaccessible fertility services. Data from the Effects of Aspirin in Gestation and Reproduction (EAGeR) Trial has
shown that preconception low-dose Aspirin therapy increases birth rates in women with histories of pregnancy
loss when preconception chronic low-grade inflammation, determined by C-reactive protein, is present. There is
a critical need to understand pathways that result in preconception chronic low-grade inflammation. This would
help to identify a broader group of women whom would benefit from aspirin therapy and inform the use of aspirin
in reproductive medicine. We hypothesize that prior exposure to common sexually transmitted infections (STIs)
can lead to long-term immune dysregulation and defective tissue repair. Among women with histories of
pregnancy loss, STI serology may indicate subsequent risk of adverse events or represent a group of women
who would benefit from preconception anti-inflammatory therapy. Prevalent and mostly asymptomatic STIs such
as Chlamydia trachomatis and Mycoplasma genitalium can ascend to the upper genital tract causing endometrial
inflammation, tissue damage and scarring. Unfortunately, most women acquire these STIs as young adults, but
do not know they were ever infected. The concept of “trained innate immunity” posits that innate immune cells
can develop a long-term proinflammatory phenotype following infectious stimuli induced through epigenetic
changes to immune and epithelial cells. Indeed, these STIs are linked to tubal infertility but associations with
other measures of impaired fecundity are limited. The specific aims of this proposal will: 1) determine if
seropositivity to Chlamydia trachomatis and Mycoplasma genitalium influences time-to-pregnancy, pregnancy
loss and birth rates in women with histories of pregnancy loss while adjusting for other STIs known to infect the
upper genital tract. 2) Determine if STI seropositive women have a unique blood immune and angiogenic profile
compared to seronegative women. 3) Determine if STI seropositive women previously randomized to Aspirin
therapy as part of the EAGeR trial (results described above) have improved birth outcomes. This study will
include 1078 women from the EAGeR trial. All women have histories of pregnancy loss but no history of infertility.
Access to preconception data from a study with extremely detailed reproductive outcomes is unique. Additionally,
our team includes a world-leader in STI diagnostics, which allows for robust serological measurements. We will
also leverage the expertise of our team members, currently funded to develop methods to address
generalizability, to transport our results to our target population of US women with histories of pregnancy loss
using the National Survey of Family Growth. Given the profound increase in STI prevalence in the U.S. and the
frequency of pregnancy loss, this study and our future work could impact a large number of women.
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Evaluating the intersection between sexually transmitted infections, inflammation and reproductive success
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批准号:10338181
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项目类别:
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资助金额:$45.56万
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财政年份:2020
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负责人:Brandie DePaoli Taylor
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依托单位:
Evaluating the intersection between sexually transmitted infections, inflammation and reproductive success
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资助金额:$40.39万
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负责人:Brandie DePaoli Taylor
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Evaluating the intersection between sexually transmitted infections, inflammation and reproductive success
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批准号:10576339
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资助金额:$46.36万
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负责人:Brandie DePaoli Taylor
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Evaluating the intersection between sexually transmitted infections, inflammation and reproductive success
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批准号:9887442
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项目类别:
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资助金额:$49.28万
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财政年份:2020
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负责人:Brandie DePaoli Taylor
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Immune activating syncytiotrophoblast microvesicles and danger associated molecular patterns in preeclampsia risk
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批准号:10437699
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项目类别:
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资助金额:$50.73万
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财政年份:2019
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负责人:Brandie DePaoli Taylor
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依托单位:
Immune activating syncytiotrophoblast microvesicles and danger associated molecular patterns in preeclampsia risk
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批准号:10655445
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项目类别:
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资助金额:$50.37万
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财政年份:2019
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负责人:Brandie DePaoli Taylor
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依托单位:
Immune activating syncytiotrophoblast microvesicles and danger associated molecular patterns in preeclampsia risk
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批准号:10441912
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项目类别:
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资助金额:$54.9万
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财政年份:2019
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负责人:Brandie DePaoli Taylor
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依托单位:
海外基金