Identification and Characterization of the Methylation Abnormalities on Whole Genome Among Infertile Men

NCT ID: NCT01239186

Last Updated: 2013-08-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

49 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-06-30

Study Completion Date

2012-12-31

Brief Summary

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This study will analyse the sperm global methylation status of 62 infertile men before assisted reproductive techniques. Some of these patients (20%) present hypomethylation of H19 locus. A global methylation analysis may reveal others imprinting defects.

Detailed Description

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An increase of the abnormalities of the imprint was brought back at the child's stemming from assisted reproductive techniques. Now abnormalities of methylation could be implied in defects of spermatogenesis and certain abnormalities of development of the male germ cells could be due to modifications abnormal epigenetics.

The objective of this research is to determine the frequency of arisen the abnormalities of methylation at the level of the locus H19 in the sperm cells of barren men presenting an unexplained oligozoospermia and to determine if these changes are a reflection of abnormalities of the profiles of methylation of the whole genome.

The patients will realize a taking of sperm having signed the consent.

Conditions

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Oligospermia

Keywords

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methylation micro array locus H19 male infertility

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Oligozoospermia

infertile patients presenting a reduced sperm count (less than 20 Millions of spermatozoa/ml)

methylation analyses on spermatozoa from infertile men

Intervention Type OTHER

microarray analysis(www.EPIGENOMICS.com)

Interventions

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methylation analyses on spermatozoa from infertile men

microarray analysis(www.EPIGENOMICS.com)

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Men from 18 to 45 years old, presenting an idiopathic oligozoospermia lower than 10 million sperm cells / ml and include in a program of medically assisted conception
* Patients with social security
* Patients having signed the informed consent

Exclusion Criteria

* Infertility with a neoplastic origin: patients subjected to a treatment potentially sterilizing (chemotherapy or radiotherapy).
* Infertility with an infectious origin
* Infertility with a traumatic origin
* Infertility bound to a chromosomal abnormality or a microdeletion of Y
* Histories of cryptorchidism, of varicocele
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Célia Ravel, MD

Role: PRINCIPAL_INVESTIGATOR

TENON Hospital - APHP

Locations

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Department of Biology of reproduction (TENON Hospital)

Paris, Île-de-France Region, France

Site Status

Countries

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France

References

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Reference Type BACKGROUND
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Reference Type BACKGROUND
PMID: 15933200 (View on PubMed)

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Reference Type BACKGROUND
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Reference Type BACKGROUND
PMID: 1393072 (View on PubMed)

Davis TL, Yang GJ, McCarrey JR, Bartolomei MS. The H19 methylation imprint is erased and re-established differentially on the parental alleles during male germ cell development. Hum Mol Genet. 2000 Nov 22;9(19):2885-94. doi: 10.1093/hmg/9.19.2885.

Reference Type BACKGROUND
PMID: 11092765 (View on PubMed)

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Reference Type BACKGROUND
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Reference Type BACKGROUND
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Kaiser J. Developmental biology. Endocrine disrupters trigger fertility problems in multiple generations. Science. 2005 Jun 3;308(5727):1391-2. doi: 10.1126/science.308.5727.1391a. No abstract available.

Reference Type BACKGROUND
PMID: 15933166 (View on PubMed)

Kobayashi H, Sato A, Otsu E, Hiura H, Tomatsu C, Utsunomiya T, Sasaki H, Yaegashi N, Arima T. Aberrant DNA methylation of imprinted loci in sperm from oligospermic patients. Hum Mol Genet. 2007 Nov 1;16(21):2542-51. doi: 10.1093/hmg/ddm187. Epub 2007 Jul 17.

Reference Type BACKGROUND
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Reference Type BACKGROUND
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Preiksa RT, Zilaitiene B, Matulevicius V, Skakkebaek NE, Petersen JH, Jorgensen N, Toppari J. Higher than expected prevalence of congenital cryptorchidism in Lithuania: a study of 1204 boys at birth and 1 year follow-up. Hum Reprod. 2005 Jul;20(7):1928-32. doi: 10.1093/humrep/deh887. Epub 2005 Apr 28.

Reference Type BACKGROUND
PMID: 15860495 (View on PubMed)

Skakkebaek NE, Rajpert-De Meyts E, Main KM. Testicular dysgenesis syndrome: an increasingly common developmental disorder with environmental aspects. Hum Reprod. 2001 May;16(5):972-8. doi: 10.1093/humrep/16.5.972.

Reference Type BACKGROUND
PMID: 11331648 (View on PubMed)

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Reference Type BACKGROUND
PMID: 8880001 (View on PubMed)

Other Identifiers

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AOR 08027

Identifier Type: -

Identifier Source: org_study_id