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Maternal Serum Cytokine Levels and Angiogenic Factor Levels in IVF vs Spontaneously Conceived Pregnancies

2009년 9월 17일 업데이트: MemorialCare

Maternal Serum Cytokine Levels and Angiogenic Factor Levels in Singleton IVF Pregnancies vs Spontaneously Conceived Pregnancies

The objective of the study is to compare maternal levels of cytokines and angiogenic factors in IVF vs spontaneously conceived singleton pregnancies. The null hypothesis is that there will be no significant difference.

연구 개요

상태

알려지지 않은

정황

상세 설명

IVF subjects: Subjects will be screened for participation at the Magella Office in Long Beach. Healthy patients with singleton pregnancies conceived with ART will be invited to participate.

Control subjects: A group of control subjects with spontaneously conceived, singleton pregnancies matched for age, parity, and race, will be identified at our Magella offices in Long Beach.

Sample size: 20 IVF subjects and 20 control subjects will be enrolled. A power analysis was performed using an alpha error of 0.05 and beta error of 0.80. Calculations were made for a 30% difference in the most studied markers during each trimester. The specific markers used in the power analysis were VEGF, sFlt, sEng, PlGF, IL-6, IL-8, TGF-beta1, and TNF-alpha. Using the values for the markers with the most stringent criteria it was determined that 15 patients would be required in each group to demonstrate a significant difference using a p value of 0.05. In anticipation of a 20-25% drop out rate, 20 subjects will be enrolled in each arm.

Specimens will be obtained at the specified intervals. Venipuncture will be performed and no more than 20 ml of blood will be obtained.

Within 2 hours of the blood draw, the blood will be spun at 2000 rpm for 10 minutes. The plasma layer will then be collected into 1 ml aliquots and stored frozen at -80°C. Upon completion of specimen collection, assays will be performed by personnel who are unaware of the outcome of the pregnancy. The markers being evaluated are not currently routinely used in clinical practice thus preventing a retrospective analysis.

The cytokine analysis and VEGF measurements will be performed using Cytokine 29 Plex Kit Premixed Beads, HCYTO-60K-PMX29 (Linco Research, St. Charles, MO, USA). This kit measures various markers and proteins of the immune system to determine the degree of inflammation. Cytokines measured with the kit include: Human IL-1, Human IL-2, Human IL-1ra, Human IL-4, Human IL-5, Human EGF, Human IL-6, Human IL-7, Human TGF,_Human Fractalkine, Human IL-8, Human IL-10, Human IL-12p70, Human IL-13, Human IL-15, Human IL-17, Human IL-1, Human IFNgamma, Human G-CSF, Human GM-CSF, Human TNF, Human Eotaxin, Human MCP-1, Human sCD40L, Human IL-12p40, Human MIP-1, Human MIP-1beta, Human IP-10, and Human VEGF.

The assays will be run according to the established protocol using the 96 well plate provided. Briefly, each serum sample is to be incubated with cytokine microbeads for 1 hour at room temperature. After washing two times, the beads will be incubated with detection antibodies for 30 min. The beads will then be combined with streptavidin-phycoerythrin and remain at room temperature for an additional 30 minutes. After two additional washings, the beads will be resuspended in assay buffer for five minutes and then the beads are to be read on the Luminex Instrument.

Commercially available enzyme-linked immunosorbent assays (ELISAs) for sFlt 1 (BioSource™) (Invitrogen Corporation, Carlsbad, CA), endoglin (R&D Systems Inc, Minneapolis, MN), PIGF (R&D Systems, Inc. Minneapolis, MN) will be used according to established protocols. Briefly, various samples for ELISA measurement will be diluted in respective calibrator diluent. After adding assay diluent, the diluted sample will be placed in a 96-well plate precoated with captured antibodies directed against human sFlt-1, human endoglin, or PlGF, and the plates were incubated for 2 hours. The wells will be washed 4 times in wash buffer and incubated with secondary polyclonal antibody against sFlt-1, endoglin, and PIGF conjugated to horseradish peroxidase for an additional 2 hours. The plates are then washed 4 times in wash buffer.

Substrate solution containing hydrogen peroxide and tetramethylbenzidine will then be added to each well and incubated for 30 minutes under protection from light with stop solution was added to each well also. The optical density will then be determined by subtracting readings at 540 nm from the reading at 450 nm. Protein levels will be calculated using a standard curve derived from a known concentration of respective recombinant proteins. The minimum detectable doses in the assay for sFlt-1, endoglin, and PlGF are 3.5, 7, and 5 pg/mL, respectively. Intraassay and interassay coefficients of variation of 3.5% and 5.5%, respectively, for sFlt-1, 3.2% and 6.5%, respectively, for endoglin, and 6% and 11%, respectively for PlGF.

Following delivery placental biopsies will be obtained for possible further analysis in anticipation of extramural funding pending the results of this study. For each placenta, three small full-thickness samples approximately 2 cm x 2 cm x 2 cm, not to include fetal membranes, will be obtained and stored in a -80ºC freezer pending mRNA extraction. We will follow a standard protocol for placental tissue harvest. The remainder of the placentas will be disposed of per routine on the Labor and Delivery unit.

Additionally, umbilical artery blood will also be obtained following delivery for possible further analysis. Within 2 hours of the blood collection, the blood will be spun at 3000 rpm for 10 minutes. The plasma layer will then be collected into 1ml aliquots and frozen in a -80ºC freezer.

For each subject, maternal demographic information including age, ethnicity, infertility history, previous obstetrical history, pregnancy complications and delivery outcomes will be collected. In addition, neonatal outcome data will be collected including delivery data, birth weight, and complications. See attached data sheet (Appendix B).

All specimens and data from the medical record will be collected and assigned a unique case number. Identifying information (e.g. name, birth date, and medical record number) will not be present in this database. In order to enable us to retrieve the medical record in the future for data verification, a key relating case numbers and medical record numbers will be kept separately. This key will be password protected, with the password only known to the investigators.

With the above exceptions, throughout the course of their pregnancy study participants will receive standard prenatal care as determined by their physicians.

Data Analysis

Categorical data will be analyzed using the Fisher exact test and chi squared test. Student t test and Mann-Whitney U tests will be used for the evaluation of parametric and non parametric continuous data, respectively.

연구 유형

관찰

등록 (예상)

40

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • California
      • Long Beach, California, 미국, 90806
        • 모병
        • MemorialCare
        • 연락하다:
          • Robert M Ehsanipoor, MD
          • 전화번호: 562-933-2755
          • 이메일: rehsanip@uci.edu
        • 수석 연구원:
          • Kenneth Chan, MD

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 (성인)

건강한 자원 봉사자를 받아들입니다

예

연구 대상 성별

여성

샘플링 방법

비확률 샘플

연구 인구

Healthy patients with singleton pregnancies conceived with ART. Only subjects that are already pregnant and have confirmed singleton intrauterine pregnancies are eligible.

설명

Inclusion Criteria:

  • Healthy patients with singleton pregnancies conceived with ART and control subjects with spontaneously conceived pregnancies. Only subjects that are already pregnant and have confirmed singleton intrauterine pregnancies are eligible.

Exclusion Criteria:

  • Subjects with hypertension, diabetes, renal disease, illicit drug use, tobacco use, morbid obesity, collagen vascular disease, and autoimmune diseases will be excluded from participation.
  • Pregnancies that had more than one gestation viewed on ultrasound at any time will be excluded.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

코호트 및 개입

그룹/코호트
1 IVF
Pregnancies conceived with the use of assisted reproductive technologies. This is defined as a pregnancy conceived with all gametes being handled outside of the body.
2 Control
Spontaneously conceived pregnancies.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
sFlt, human endoglin, PlGF, VEGF, IL-1, IL-2, IL-1ra, IL-4, IL-5, EGF, IL-6, Human IL-7, TGF, Fractalkine, IL-8, IL-10, IL-12p70, IL-13, IL-15, IL-17, IL-1, IFN-gamma, G-CSF, GM-CSF, TNF, Eotaxin, MCP-1, sCD40L, IL-12p40, MIP-1, MIP-1ß, IP-10
기간: 10 months
10 months

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

수사관

  • 수석 연구원: Kenneth Chan, MD, MemorialCare

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2008년 6월 1일

기본 완료 (예상)

2010년 3월 1일

연구 완료 (예상)

2010년 6월 1일

연구 등록 날짜

최초 제출

2009년 2월 4일

QC 기준을 충족하는 최초 제출

2009년 2월 4일

처음 게시됨 (추정)

2009년 2월 5일

연구 기록 업데이트

마지막 업데이트 게시됨 (추정)

2009년 9월 18일

QC 기준을 충족하는 마지막 업데이트 제출

2009년 9월 17일

마지막으로 확인됨

2009년 9월 1일

추가 정보

이 연구와 관련된 용어

추가 관련 MeSH 약관

기타 연구 ID 번호

  • IVF cytokines
  • MHS IRB No. 525-08

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

구독하다