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

2009年9月17日 更新者: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.

調査の概要

状態

わからない

条件

詳細な説明

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.

研究の種類

観察的

入学 (予想される)

40

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • California
      • Long Beach、California、アメリカ、90806
        • 募集
        • MemorialCare
        • コンタクト:
          • Robert M Ehsanipoor, MD
          • 電話番号:562-933-2755
          • メール:rehsanip@uci.edu
        • 主任研究者:
          • Kenneth Chan, MD

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年~50年 (大人)

健康ボランティアの受け入れ

はい

受講資格のある性別

女性

サンプリング方法

非確率サンプル

調査対象母集団

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

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

コホートと介入

グループ/コホート
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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
時間枠
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
時間枠:10 months
10 months

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Kenneth Chan, MD、MemorialCare

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始

2008年6月1日

一次修了 (予想される)

2010年3月1日

研究の完了 (予想される)

2010年6月1日

試験登録日

最初に提出

2009年2月4日

QC基準を満たした最初の提出物

2009年2月4日

最初の投稿 (見積もり)

2009年2月5日

学習記録の更新

投稿された最後の更新 (見積もり)

2009年9月18日

QC基準を満たした最後の更新が送信されました

2009年9月17日

最終確認日

2009年9月1日

詳しくは

本研究に関する用語

追加の関連 MeSH 用語

その他の研究ID番号

  • IVF cytokines
  • MHS IRB No. 525-08

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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