The use of fluorescence in situ hybridization analysis on sperm: indications to perform and assisted reproduction technology outcomes
Purpose To determine the consequences of an altered sperm fluorescence in situ hybridization (FISH) result for ART outcomes and the indications for a sperm FISH analysis. Methods Data from 439 infertile men were collected. Bivariate analyses were performed to determine the association of men’s age,...
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Veröffentlicht in: | Journal of assisted reproduction and genetics 2019-10, Vol.36 (10), p.1975-1987 |
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container_end_page | 1987 |
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container_issue | 10 |
container_start_page | 1975 |
container_title | Journal of assisted reproduction and genetics |
container_volume | 36 |
creator | Sarrate, Zaida Blanco, Joan Marina-Rugero, Fernando Moreno-García, Juan Manuel Ruiz-Jorro, Miguel Lafuente-Varea, Rafael Graña-Zanón, Fernando Núñez-Calonge, Rocío Ten, Jorge Rueda, Joaquín |
description | Purpose
To determine the consequences of an altered sperm fluorescence in situ hybridization (FISH) result for ART outcomes and the indications for a sperm FISH analysis.
Methods
Data from 439 infertile men were collected. Bivariate analyses were performed to determine the association of men’s age, seminal alterations, and sperm FISH indication, with the incidence of X, Y, 13, 18, and 21 sperm chromosomal abnormalities. A multivariate logistic regression analysis was performed to establish the most predictive variables for altered sperm FISH. Results from the IVF/ICSI cycles were collected for 248 out of 439 patients. Two distinct groups were established: 151 couples that used their own oocytes and 97 couples involved in egg donation programs. In both groups, ART outcomes were compared between normal and altered sperm FISH.
Results
Teratozoospermia and oligozoospermia were associated with sperm chromosome anomalies (
p
< 0.05). Indications for sperm FISH analysis with the highest predictability were teratozoospermia, male age, oligozoospermia, and implantation failure (AUC = 0.702). Embryo quality (
p
= 0.096), pregnancy rate (
p
= 0.054), and implantation rate (
p
= 0.089) were higher in own-oocytes couples with normal sperm FISH than in altered sperm FISH couples, although differences were not statistically significant. In donor-oocytes couples, in which high-quality embryos were transferred later than in own-oocytes couples (3.8 vs. 3.0 days), we did not identify differences in the ART outcome between normal and altered sperm FISH couples. In both groups, the possible interference of woman age was negligible.
Conclusions
Sperm FISH is indicated in middle-aged oligoteratozoospermic patients with implantation failures in previous IVF/ICSI cycles. Sperm chromosome anomalies have a moderate detrimental impact on embryo quality, implantation, and pregnancy rates. |
doi_str_mv | 10.1007/s10815-019-01554-2 |
format | Article |
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To determine the consequences of an altered sperm fluorescence in situ hybridization (FISH) result for ART outcomes and the indications for a sperm FISH analysis.
Methods
Data from 439 infertile men were collected. Bivariate analyses were performed to determine the association of men’s age, seminal alterations, and sperm FISH indication, with the incidence of X, Y, 13, 18, and 21 sperm chromosomal abnormalities. A multivariate logistic regression analysis was performed to establish the most predictive variables for altered sperm FISH. Results from the IVF/ICSI cycles were collected for 248 out of 439 patients. Two distinct groups were established: 151 couples that used their own oocytes and 97 couples involved in egg donation programs. In both groups, ART outcomes were compared between normal and altered sperm FISH.
Results
Teratozoospermia and oligozoospermia were associated with sperm chromosome anomalies (
p
< 0.05). Indications for sperm FISH analysis with the highest predictability were teratozoospermia, male age, oligozoospermia, and implantation failure (AUC = 0.702). Embryo quality (
p
= 0.096), pregnancy rate (
p
= 0.054), and implantation rate (
p
= 0.089) were higher in own-oocytes couples with normal sperm FISH than in altered sperm FISH couples, although differences were not statistically significant. In donor-oocytes couples, in which high-quality embryos were transferred later than in own-oocytes couples (3.8 vs. 3.0 days), we did not identify differences in the ART outcome between normal and altered sperm FISH couples. In both groups, the possible interference of woman age was negligible.
Conclusions
Sperm FISH is indicated in middle-aged oligoteratozoospermic patients with implantation failures in previous IVF/ICSI cycles. Sperm chromosome anomalies have a moderate detrimental impact on embryo quality, implantation, and pregnancy rates.</description><identifier>ISSN: 1058-0468</identifier><identifier>EISSN: 1573-7330</identifier><identifier>DOI: 10.1007/s10815-019-01554-2</identifier><identifier>PMID: 31396849</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adult ; Age ; Assisted Reproduction Technologies ; Chromosome Aberrations ; Egg donations ; Embryo Implantation - genetics ; Embryo Implantation - physiology ; Embryos ; Female ; Fertilization in Vitro - methods ; Fluorescence in situ hybridization ; Gynecology ; Human Genetics ; Humans ; Hybridization analysis ; Implantation ; In Situ Hybridization, Fluorescence ; Male ; Medicine ; Medicine & Public Health ; Middle Aged ; Oligospermia - diagnosis ; Oligospermia - genetics ; Oligospermia - pathology ; Oligozoospermia ; Oocytes ; Pregnancy ; Pregnancy Rate ; Reproductive Medicine ; Reproductive Techniques, Assisted ; Sperm ; Sperm Injections, Intracytoplasmic - methods ; Spermatozoa - pathology ; Spermatozoa - ultrastructure ; Statistical analysis ; Teratozoospermia - diagnosis ; Teratozoospermia - genetics ; Teratozoospermia - pathology ; Tissue Donors</subject><ispartof>Journal of assisted reproduction and genetics, 2019-10, Vol.36 (10), p.1975-1987</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2019</rights><rights>Journal of Assisted Reproduction and Genetics is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-e7e7469aaf7fbccc7403d1d078b2fad76c532e409fae7f03c6e77b84c66a1d743</citedby><cites>FETCH-LOGICAL-c474t-e7e7469aaf7fbccc7403d1d078b2fad76c532e409fae7f03c6e77b84c66a1d743</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6823339/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6823339/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,41464,42533,51294,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31396849$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sarrate, Zaida</creatorcontrib><creatorcontrib>Blanco, Joan</creatorcontrib><creatorcontrib>Marina-Rugero, Fernando</creatorcontrib><creatorcontrib>Moreno-García, Juan Manuel</creatorcontrib><creatorcontrib>Ruiz-Jorro, Miguel</creatorcontrib><creatorcontrib>Lafuente-Varea, Rafael</creatorcontrib><creatorcontrib>Graña-Zanón, Fernando</creatorcontrib><creatorcontrib>Núñez-Calonge, Rocío</creatorcontrib><creatorcontrib>Ten, Jorge</creatorcontrib><creatorcontrib>Rueda, Joaquín</creatorcontrib><title>The use of fluorescence in situ hybridization analysis on sperm: indications to perform and assisted reproduction technology outcomes</title><title>Journal of assisted reproduction and genetics</title><addtitle>J Assist Reprod Genet</addtitle><addtitle>J Assist Reprod Genet</addtitle><description>Purpose
To determine the consequences of an altered sperm fluorescence in situ hybridization (FISH) result for ART outcomes and the indications for a sperm FISH analysis.
Methods
Data from 439 infertile men were collected. Bivariate analyses were performed to determine the association of men’s age, seminal alterations, and sperm FISH indication, with the incidence of X, Y, 13, 18, and 21 sperm chromosomal abnormalities. A multivariate logistic regression analysis was performed to establish the most predictive variables for altered sperm FISH. Results from the IVF/ICSI cycles were collected for 248 out of 439 patients. Two distinct groups were established: 151 couples that used their own oocytes and 97 couples involved in egg donation programs. In both groups, ART outcomes were compared between normal and altered sperm FISH.
Results
Teratozoospermia and oligozoospermia were associated with sperm chromosome anomalies (
p
< 0.05). Indications for sperm FISH analysis with the highest predictability were teratozoospermia, male age, oligozoospermia, and implantation failure (AUC = 0.702). Embryo quality (
p
= 0.096), pregnancy rate (
p
= 0.054), and implantation rate (
p
= 0.089) were higher in own-oocytes couples with normal sperm FISH than in altered sperm FISH couples, although differences were not statistically significant. In donor-oocytes couples, in which high-quality embryos were transferred later than in own-oocytes couples (3.8 vs. 3.0 days), we did not identify differences in the ART outcome between normal and altered sperm FISH couples. In both groups, the possible interference of woman age was negligible.
Conclusions
Sperm FISH is indicated in middle-aged oligoteratozoospermic patients with implantation failures in previous IVF/ICSI cycles. Sperm chromosome anomalies have a moderate detrimental impact on embryo quality, implantation, and pregnancy rates.</description><subject>Adult</subject><subject>Age</subject><subject>Assisted Reproduction Technologies</subject><subject>Chromosome Aberrations</subject><subject>Egg donations</subject><subject>Embryo Implantation - genetics</subject><subject>Embryo Implantation - physiology</subject><subject>Embryos</subject><subject>Female</subject><subject>Fertilization in Vitro - methods</subject><subject>Fluorescence in situ hybridization</subject><subject>Gynecology</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Hybridization analysis</subject><subject>Implantation</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Oligospermia - diagnosis</subject><subject>Oligospermia - genetics</subject><subject>Oligospermia - pathology</subject><subject>Oligozoospermia</subject><subject>Oocytes</subject><subject>Pregnancy</subject><subject>Pregnancy Rate</subject><subject>Reproductive Medicine</subject><subject>Reproductive Techniques, Assisted</subject><subject>Sperm</subject><subject>Sperm Injections, Intracytoplasmic - methods</subject><subject>Spermatozoa - pathology</subject><subject>Spermatozoa - ultrastructure</subject><subject>Statistical analysis</subject><subject>Teratozoospermia - diagnosis</subject><subject>Teratozoospermia - genetics</subject><subject>Teratozoospermia - pathology</subject><subject>Tissue Donors</subject><issn>1058-0468</issn><issn>1573-7330</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kT1vFDEQhi1ERELgD1AgS9QL_lp7TYGEIr6kSGmS2vLa4ztHu-vD9iJdev43zl0I0FBYHs088449L0KvKHlLCVHvCiUD7TtCdTt9Lzr2BJ3RXvFOcU6etpj0Q0eEHE7R81JuCSF6YPwZOuWUazkIfYZ-Xm8BrwVwCjhMa8pQHCwOcFxwiXXF2_2Yo493tsa0YLvYaV9iwS0uO8jz-wb66A7VgmvCLRlSnhvpsS0NreBxhl1OfnUHjQpuu6QpbfY4rdWlGcoLdBLsVODlw32Obj5_ur742l1effl28fGyc0KJ2oECJaS2NqgwOueUINxTT9QwsmC9kq7nDATRwYIKhDsJSo2DcFJa6pXg5-jDUXe3jjP49tOa7WR2Oc42702y0fxbWeLWbNIPI9veONdN4M2DQE7fVyjV3KY1t6UUw5jUSjNKVaPYkXI5lZIhPE6gxNxbZ47WmWadOVhnWGt6_ffbHlt-e9UAfgRKKy0byH9m_0f2F6v0qcc</recordid><startdate>20191001</startdate><enddate>20191001</enddate><creator>Sarrate, Zaida</creator><creator>Blanco, Joan</creator><creator>Marina-Rugero, Fernando</creator><creator>Moreno-García, Juan Manuel</creator><creator>Ruiz-Jorro, Miguel</creator><creator>Lafuente-Varea, Rafael</creator><creator>Graña-Zanón, Fernando</creator><creator>Núñez-Calonge, Rocío</creator><creator>Ten, Jorge</creator><creator>Rueda, Joaquín</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20191001</creationdate><title>The use of fluorescence in situ hybridization analysis on sperm: indications to perform and assisted reproduction technology outcomes</title><author>Sarrate, Zaida ; Blanco, Joan ; Marina-Rugero, Fernando ; Moreno-García, Juan Manuel ; Ruiz-Jorro, Miguel ; Lafuente-Varea, Rafael ; Graña-Zanón, Fernando ; Núñez-Calonge, Rocío ; Ten, Jorge ; Rueda, Joaquín</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-e7e7469aaf7fbccc7403d1d078b2fad76c532e409fae7f03c6e77b84c66a1d743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Age</topic><topic>Assisted Reproduction Technologies</topic><topic>Chromosome Aberrations</topic><topic>Egg donations</topic><topic>Embryo Implantation - genetics</topic><topic>Embryo Implantation - physiology</topic><topic>Embryos</topic><topic>Female</topic><topic>Fertilization in Vitro - methods</topic><topic>Fluorescence in situ hybridization</topic><topic>Gynecology</topic><topic>Human Genetics</topic><topic>Humans</topic><topic>Hybridization analysis</topic><topic>Implantation</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Oligospermia - diagnosis</topic><topic>Oligospermia - genetics</topic><topic>Oligospermia - pathology</topic><topic>Oligozoospermia</topic><topic>Oocytes</topic><topic>Pregnancy</topic><topic>Pregnancy Rate</topic><topic>Reproductive Medicine</topic><topic>Reproductive Techniques, Assisted</topic><topic>Sperm</topic><topic>Sperm Injections, Intracytoplasmic - methods</topic><topic>Spermatozoa - pathology</topic><topic>Spermatozoa - ultrastructure</topic><topic>Statistical analysis</topic><topic>Teratozoospermia - diagnosis</topic><topic>Teratozoospermia - genetics</topic><topic>Teratozoospermia - pathology</topic><topic>Tissue Donors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sarrate, Zaida</creatorcontrib><creatorcontrib>Blanco, Joan</creatorcontrib><creatorcontrib>Marina-Rugero, Fernando</creatorcontrib><creatorcontrib>Moreno-García, Juan Manuel</creatorcontrib><creatorcontrib>Ruiz-Jorro, Miguel</creatorcontrib><creatorcontrib>Lafuente-Varea, Rafael</creatorcontrib><creatorcontrib>Graña-Zanón, Fernando</creatorcontrib><creatorcontrib>Núñez-Calonge, Rocío</creatorcontrib><creatorcontrib>Ten, Jorge</creatorcontrib><creatorcontrib>Rueda, Joaquín</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of assisted reproduction and genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sarrate, Zaida</au><au>Blanco, Joan</au><au>Marina-Rugero, Fernando</au><au>Moreno-García, Juan Manuel</au><au>Ruiz-Jorro, Miguel</au><au>Lafuente-Varea, Rafael</au><au>Graña-Zanón, Fernando</au><au>Núñez-Calonge, Rocío</au><au>Ten, Jorge</au><au>Rueda, Joaquín</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The use of fluorescence in situ hybridization analysis on sperm: indications to perform and assisted reproduction technology outcomes</atitle><jtitle>Journal of assisted reproduction and genetics</jtitle><stitle>J Assist Reprod Genet</stitle><addtitle>J Assist Reprod Genet</addtitle><date>2019-10-01</date><risdate>2019</risdate><volume>36</volume><issue>10</issue><spage>1975</spage><epage>1987</epage><pages>1975-1987</pages><issn>1058-0468</issn><eissn>1573-7330</eissn><abstract>Purpose
To determine the consequences of an altered sperm fluorescence in situ hybridization (FISH) result for ART outcomes and the indications for a sperm FISH analysis.
Methods
Data from 439 infertile men were collected. Bivariate analyses were performed to determine the association of men’s age, seminal alterations, and sperm FISH indication, with the incidence of X, Y, 13, 18, and 21 sperm chromosomal abnormalities. A multivariate logistic regression analysis was performed to establish the most predictive variables for altered sperm FISH. Results from the IVF/ICSI cycles were collected for 248 out of 439 patients. Two distinct groups were established: 151 couples that used their own oocytes and 97 couples involved in egg donation programs. In both groups, ART outcomes were compared between normal and altered sperm FISH.
Results
Teratozoospermia and oligozoospermia were associated with sperm chromosome anomalies (
p
< 0.05). Indications for sperm FISH analysis with the highest predictability were teratozoospermia, male age, oligozoospermia, and implantation failure (AUC = 0.702). Embryo quality (
p
= 0.096), pregnancy rate (
p
= 0.054), and implantation rate (
p
= 0.089) were higher in own-oocytes couples with normal sperm FISH than in altered sperm FISH couples, although differences were not statistically significant. In donor-oocytes couples, in which high-quality embryos were transferred later than in own-oocytes couples (3.8 vs. 3.0 days), we did not identify differences in the ART outcome between normal and altered sperm FISH couples. In both groups, the possible interference of woman age was negligible.
Conclusions
Sperm FISH is indicated in middle-aged oligoteratozoospermic patients with implantation failures in previous IVF/ICSI cycles. Sperm chromosome anomalies have a moderate detrimental impact on embryo quality, implantation, and pregnancy rates.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>31396849</pmid><doi>10.1007/s10815-019-01554-2</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Springer Nature - Complete Springer Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Adult Age Assisted Reproduction Technologies Chromosome Aberrations Egg donations Embryo Implantation - genetics Embryo Implantation - physiology Embryos Female Fertilization in Vitro - methods Fluorescence in situ hybridization Gynecology Human Genetics Humans Hybridization analysis Implantation In Situ Hybridization, Fluorescence Male Medicine Medicine & Public Health Middle Aged Oligospermia - diagnosis Oligospermia - genetics Oligospermia - pathology Oligozoospermia Oocytes Pregnancy Pregnancy Rate Reproductive Medicine Reproductive Techniques, Assisted Sperm Sperm Injections, Intracytoplasmic - methods Spermatozoa - pathology Spermatozoa - ultrastructure Statistical analysis Teratozoospermia - diagnosis Teratozoospermia - genetics Teratozoospermia - pathology Tissue Donors |
title | The use of fluorescence in situ hybridization analysis on sperm: indications to perform and assisted reproduction technology outcomes |
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