Integrated treatment guided by RNA-seq–based endometrial receptivity assessment for infertility complicated by MEN1
Preimplantation genetic testing (PGT) serves as a tool to avoid genetic disorders in patients with known genetic conditions. However, once a selected embryo is transferred, implantation success is attained independent of embryo quality. Using PGT alone is unable to tackle implantation failure caused...
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Published in | Frontiers in endocrinology (Lausanne) Vol. 14; p. 1224574 |
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Abstract | Preimplantation genetic testing (PGT) serves as a tool to avoid genetic disorders in patients with known genetic conditions. However, once a selected embryo is transferred, implantation success is attained independent of embryo quality. Using PGT alone is unable to tackle implantation failure caused by endometrial receptivity (ER) abnormalities in these patients.BackgroundPreimplantation genetic testing (PGT) serves as a tool to avoid genetic disorders in patients with known genetic conditions. However, once a selected embryo is transferred, implantation success is attained independent of embryo quality. Using PGT alone is unable to tackle implantation failure caused by endometrial receptivity (ER) abnormalities in these patients.We validated our newly developed RNA-seq-based ER test (rsERT) in a retrospective cohort study including 511 PGT cycles and reported experience in treating an infertile female patient complicated by multiple endocrine neoplasia type 1 (MEN1).MethodsWe validated our newly developed RNA-seq-based ER test (rsERT) in a retrospective cohort study including 511 PGT cycles and reported experience in treating an infertile female patient complicated by multiple endocrine neoplasia type 1 (MEN1).Significant improvement in the clinical pregnancy rate was found in the performed personalized embryo transfer (pET) group (CR, 69.7%; P = 0.035). In the rare MEN1 case, pET was done according to the prediction of the optimal time of window of implantation after unaffected blastocysts were obtained by PGT-M, which ultimately led to a healthy live birth. However, none of the mRNA variants identified in the patient showed a strong association with the MEN1 gene.ResultsSignificant improvement in the clinical pregnancy rate was found in the performed personalized embryo transfer (pET) group (CR, 69.7%; P = 0.035). In the rare MEN1 case, pET was done according to the prediction of the optimal time of window of implantation after unaffected blastocysts were obtained by PGT-M, which ultimately led to a healthy live birth. However, none of the mRNA variants identified in the patient showed a strong association with the MEN1 gene.Applying the new rsERT along with PGT improved ART outcomes and brought awareness of the importance of the ER examination in MEN1 infertile female patients. MEN1-induced endocrine disorder rather than MEN1 mutation contributes to the ER abnormality.ConclusionsApplying the new rsERT along with PGT improved ART outcomes and brought awareness of the importance of the ER examination in MEN1 infertile female patients. MEN1-induced endocrine disorder rather than MEN1 mutation contributes to the ER abnormality.Reproductive Medicine Ethics Committee of Xiangya Hospital Registry No.: 2022010.Trial RegistrationReproductive Medicine Ethics Committee of Xiangya Hospital Registry No.: 2022010. |
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AbstractList | BackgroundPreimplantation genetic testing (PGT) serves as a tool to avoid genetic disorders in patients with known genetic conditions. However, once a selected embryo is transferred, implantation success is attained independent of embryo quality. Using PGT alone is unable to tackle implantation failure caused by endometrial receptivity (ER) abnormalities in these patients.MethodsWe validated our newly developed RNA-seq–based ER test (rsERT) in a retrospective cohort study including 511 PGT cycles and reported experience in treating an infertile female patient complicated by multiple endocrine neoplasia type 1 (MEN1).ResultsSignificant improvement in the clinical pregnancy rate was found in the performed personalized embryo transfer (pET) group (CR, 69.7%; P = 0.035). In the rare MEN1 case, pET was done according to the prediction of the optimal time of window of implantation after unaffected blastocysts were obtained by PGT-M, which ultimately led to a healthy live birth. However, none of the mRNA variants identified in the patient showed a strong association with the MEN1 gene.ConclusionsApplying the new rsERT along with PGT improved ART outcomes and brought awareness of the importance of the ER examination in MEN1 infertile female patients. MEN1-induced endocrine disorder rather than MEN1 mutation contributes to the ER abnormality.Trial RegistrationReproductive Medicine Ethics Committee of Xiangya Hospital Registry No.: 2022010. Preimplantation genetic testing (PGT) serves as a tool to avoid genetic disorders in patients with known genetic conditions. However, once a selected embryo is transferred, implantation success is attained independent of embryo quality. Using PGT alone is unable to tackle implantation failure caused by endometrial receptivity (ER) abnormalities in these patients.BackgroundPreimplantation genetic testing (PGT) serves as a tool to avoid genetic disorders in patients with known genetic conditions. However, once a selected embryo is transferred, implantation success is attained independent of embryo quality. Using PGT alone is unable to tackle implantation failure caused by endometrial receptivity (ER) abnormalities in these patients.We validated our newly developed RNA-seq-based ER test (rsERT) in a retrospective cohort study including 511 PGT cycles and reported experience in treating an infertile female patient complicated by multiple endocrine neoplasia type 1 (MEN1).MethodsWe validated our newly developed RNA-seq-based ER test (rsERT) in a retrospective cohort study including 511 PGT cycles and reported experience in treating an infertile female patient complicated by multiple endocrine neoplasia type 1 (MEN1).Significant improvement in the clinical pregnancy rate was found in the performed personalized embryo transfer (pET) group (CR, 69.7%; P = 0.035). In the rare MEN1 case, pET was done according to the prediction of the optimal time of window of implantation after unaffected blastocysts were obtained by PGT-M, which ultimately led to a healthy live birth. However, none of the mRNA variants identified in the patient showed a strong association with the MEN1 gene.ResultsSignificant improvement in the clinical pregnancy rate was found in the performed personalized embryo transfer (pET) group (CR, 69.7%; P = 0.035). In the rare MEN1 case, pET was done according to the prediction of the optimal time of window of implantation after unaffected blastocysts were obtained by PGT-M, which ultimately led to a healthy live birth. However, none of the mRNA variants identified in the patient showed a strong association with the MEN1 gene.Applying the new rsERT along with PGT improved ART outcomes and brought awareness of the importance of the ER examination in MEN1 infertile female patients. MEN1-induced endocrine disorder rather than MEN1 mutation contributes to the ER abnormality.ConclusionsApplying the new rsERT along with PGT improved ART outcomes and brought awareness of the importance of the ER examination in MEN1 infertile female patients. MEN1-induced endocrine disorder rather than MEN1 mutation contributes to the ER abnormality.Reproductive Medicine Ethics Committee of Xiangya Hospital Registry No.: 2022010.Trial RegistrationReproductive Medicine Ethics Committee of Xiangya Hospital Registry No.: 2022010. |
Author | Tang, Hongying Yao, Zhongyuan Xu, Aizhuang He, Aihua Zhang, Qiong Lu, Sijia Zhao, Jing Li, Yanping Huang, Xi Liang, Shaolin Fu, Jing Xia, Qiuping |
AuthorAffiliation | 4 National Comprehensive Utilization of Science and Technology Information Resources and Public Service Center, Scientific and Technical Information (STI)-Zhilian Research Institute for Innovation and Digital Health , Beijing , China 3 Department of Reproductive Medicine Center, The Third Xiangya Hospital, Central South University , Changsha, Hunan , China 6 Institute for Six-sector Economy, Fudan University , Shanghai , China 5 ”Mobile Health” Ministry of Education-China Mobile Joint Laboratory, Xiangya Hospital, Central South University , Changsha , China 1 Department of Reproductive Medicine, Xiangya Hospital, Central South University , Changsha, Hunan , China 2 Clinical Research Center for Women’s Reproductive Health in Hunan Province , Changsha, Hunan , China 7 Department of Clinical Research, Yikon Genomics Company, Ltd. , Suzhou, Jiangsu , China |
AuthorAffiliation_xml | – name: 5 ”Mobile Health” Ministry of Education-China Mobile Joint Laboratory, Xiangya Hospital, Central South University , Changsha , China – name: 7 Department of Clinical Research, Yikon Genomics Company, Ltd. , Suzhou, Jiangsu , China – name: 3 Department of Reproductive Medicine Center, The Third Xiangya Hospital, Central South University , Changsha, Hunan , China – name: 2 Clinical Research Center for Women’s Reproductive Health in Hunan Province , Changsha, Hunan , China – name: 1 Department of Reproductive Medicine, Xiangya Hospital, Central South University , Changsha, Hunan , China – name: 4 National Comprehensive Utilization of Science and Technology Information Resources and Public Service Center, Scientific and Technical Information (STI)-Zhilian Research Institute for Innovation and Digital Health , Beijing , China – name: 6 Institute for Six-sector Economy, Fudan University , Shanghai , China |
Author_xml | – sequence: 1 givenname: Xi surname: Huang fullname: Huang, Xi – sequence: 2 givenname: Jing surname: Fu fullname: Fu, Jing – sequence: 3 givenname: Qiong surname: Zhang fullname: Zhang, Qiong – sequence: 4 givenname: Jing surname: Zhao fullname: Zhao, Jing – sequence: 5 givenname: Zhongyuan surname: Yao fullname: Yao, Zhongyuan – sequence: 6 givenname: Qiuping surname: Xia fullname: Xia, Qiuping – sequence: 7 givenname: Hongying surname: Tang fullname: Tang, Hongying – sequence: 8 givenname: Aizhuang surname: Xu fullname: Xu, Aizhuang – sequence: 9 givenname: Aihua surname: He fullname: He, Aihua – sequence: 10 givenname: Shaolin surname: Liang fullname: Liang, Shaolin – sequence: 11 givenname: Sijia surname: Lu fullname: Lu, Sijia – sequence: 12 givenname: Yanping surname: Li fullname: Li, Yanping |
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Cites_doi | 10.1016/S0140-6736(20)32475-2 10.1111/cen.13890 10.1016/j.fertnstert.2010.04.063 10.1093/hropen/hoab010 10.1093/hropen/hoab011 10.3390/medicina47110092 10.1158/0008-5472.CAN-05-4461 10.1038/sj.onc.1204529 10.5935/1518-0557.20180010 10.1016/B978-0-323-47912-7.00022-6 10.1186/s12967-021-02837-y 10.4103/jhrs.JHRS_164_19 10.1210/jc.2012-1230 10.1016/s0015-0282(02)04670-8 10.1080/09513590.2021.1974382 10.1093/humrep/14.1.252 10.1054/bjoc.2000.1380 10.1016/j.fertnstert.2012.09.046 |
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Copyright | Copyright © 2023 Huang, Fu, Zhang, Zhao, Yao, Xia, Tang, Xu, He, Liang, Lu and Li. Copyright © 2023 Huang, Fu, Zhang, Zhao, Yao, Xia, Tang, Xu, He, Liang, Lu and Li 2023 Huang, Fu, Zhang, Zhao, Yao, Xia, Tang, Xu, He, Liang, Lu and Li |
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SubjectTerms | Endocrinology endometrial receptivity MEN1 personalized embryo transfer PGT-M RNA-seq |
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Title | Integrated treatment guided by RNA-seq–based endometrial receptivity assessment for infertility complicated by MEN1 |
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