Literature DB >> 33495935

Fertility preservation for genetic diseases leading to premature ovarian insufficiency (POI).

Antonio La Marca1,2, Elisa Mastellari3.   

Abstract

PURPOSE: The current review aims to summarize the data available concerning the applicability of fertility preservation techniques to genetic conditions at risk of premature ovarian insufficiency (POI).
METHODS: A literature review through the PubMed Database was carried out.
RESULTS: About 10% of cases of POI is related to genetic diseases. The most frequent conditions associated with POI are Turner syndrome and fragile X pre-mutation; mutation of BRCA 1-2 genes and several other mutations and genetic syndromes have recently been highlighted, although they rarely occur. If a diagnosis is issued before POI onset, counseling on currently available fertility preservation techniques is advisable. In case of spontaneous menarche (this can occur variably depending on the mutation) established techniques like embryo or oocyte cryopreservation can be proposed, even if, in some cases, their effectiveness may be reduced by ovarian alterations connected to the mutation. Ovarian tissue cryopreservation has recently been defined as an established medical procedure for fertility preservation in young cancer patients and may be an option for prepubertal patients. However, it is still experimental in special populations with genetic diseases causing POI. New innovative experimental techniques, like in vitro maturation of immature oocytes (IVM) and vitro activation (IVA) of immature follicles on ovarian tissue, have shown limited but encouraging data and they will be probably available in the near future. For a correct risk-benefit evaluation, the following aspects should be considered: actual knowledge about the pathology-specific efficacy of the various techniques, the average age of onset of POI, the possible risks associated with the procedure in relation to the underlying pathology, the probability of spontaneous conception, as well as the health implications of a possible future pregnancy..
CONCLUSIONS: Fertility preservation techniques represent a crucial opportunity for patients with genetic risk of POI. Early diagnosis increases the chances to apply these techniques. No specific recommendations concerning fertility preservation for each genetic pathology are available, and clinicians should first counsel the patient and her relatives about known risks and benefits of the available techniques, both those established and those considered as experimental.

Entities:  

Keywords:  BRCA; Cryopreservation; FMR1; Fertility; Genetic; Ovarian insufficiency; Turner

Mesh:

Substances:

Year:  2021        PMID: 33495935      PMCID: PMC8079553          DOI: 10.1007/s10815-021-02067-7

Source DB:  PubMed          Journal:  J Assist Reprod Genet        ISSN: 1058-0468            Impact factor:   3.412


  112 in total

Review 1.  Fertility Preservation in Women with Turner Syndrome: A Comprehensive Review and Practical Guidelines.

Authors:  Kutluk Oktay; Giuliano Bedoschi; Karen Berkowitz; Richard Bronson; Banafsheh Kashani; Peter McGovern; Lubna Pal; Gwendolyn Quinn; Karen Rubin
Journal:  J Pediatr Adolesc Gynecol       Date:  2015-10-17       Impact factor: 1.814

Review 2.  Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency.

Authors:  Ilpo Huhtaniemi; Outi Hovatta; Antonio La Marca; Gabriel Livera; Danielle Monniaux; Luca Persani; Abdelkader Heddar; Katarzyna Jarzabek; Triin Laisk-Podar; Andres Salumets; Juha S Tapanainen; Reiner A Veitia; Jenny A Visser; Peter Wieacker; Slawomir Wolczynski; Micheline Misrahi
Journal:  Trends Endocrinol Metab       Date:  2018-04-26       Impact factor: 12.015

3.  Spontaneous pubertal development in Turner's syndrome. Italian Study Group for Turner's Syndrome.

Authors:  A M Pasquino; F Passeri; I Pucarelli; M Segni; G Municchi
Journal:  J Clin Endocrinol Metab       Date:  1997-06       Impact factor: 5.958

4.  Turner syndrome: four challenges across the lifespan.

Authors:  Erica J Sutton; Aideen McInerney-Leo; Carolyn A Bondy; Sarah E Gollust; Donnice King; Barbara Biesecker
Journal:  Am J Med Genet A       Date:  2005-12-01       Impact factor: 2.802

Review 5.  Turner syndrome: contemporary thoughts and reproductive issues.

Authors:  Richard H Reindollar
Journal:  Semin Reprod Med       Date:  2011-10-03       Impact factor: 1.303

6.  Fertility preservation in girls with turner syndrome: prognostic signs of the presence of ovarian follicles.

Authors:  Birgit Borgström; Borgström Birgit; Julius Hreinsson; Hreinsson Julius; Carsten Rasmussen; Rasmussen Carsten; Maryam Sheikhi; Sheikhi Maryam; Gabriel Fried; Fried Gabriel; Victoria Keros; Keros Victoria; Margareta Fridström; Fridström Margareta; Outi Hovatta; Hovatta Outi
Journal:  J Clin Endocrinol Metab       Date:  2008-10-28       Impact factor: 5.958

7.  Reproductive performance in women with sex chromosome mosaicism.

Authors:  D N Singh; S Hara; H W Foster; E M Grimes
Journal:  Obstet Gynecol       Date:  1980-05       Impact factor: 7.661

8.  Ovarian function and in vitro fertilization (IVF) in Turner syndrome.

Authors:  Outi Hovatta
Journal:  Pediatr Endocrinol Rev       Date:  2012-05

Review 9.  Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features.

Authors:  T Ogata; N Matsuo
Journal:  Hum Genet       Date:  1995-06       Impact factor: 4.132

10.  Reproductive and obstetric outcomes in mosaic Turner's Syndrome: a cross-sectional study and review of the literature.

Authors:  Emek Doğer; Yiğit Çakıroğlu; Yasin Ceylan; Esen Ulak; Özkan Özdamar; Eray Çalışkan
Journal:  Reprod Biol Endocrinol       Date:  2015-06-10       Impact factor: 5.211

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  3 in total

1.  Identification and Validation of Autophagy-Related Genes in Primary Ovarian Insufficiency by Gene Expression Profile and Bioinformatic Analysis.

Authors:  Siji Lv; Jiani Sun; Jing Sun
Journal:  Anal Cell Pathol (Amst)       Date:  2022-07-04       Impact factor: 4.133

2.  Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency.

Authors:  Ayberk Turkyilmaz; Ceren Alavanda; Esra Arslan Ates; Bilgen Bilge Geckinli; Hamza Polat; Mehmet Gokcu; Taner Karakaya; Alper Han Cebi; Mehmet Ali Soylemez; Ahmet İlter Guney; Pinar Ata; Ahmet Arman
Journal:  J Assist Reprod Genet       Date:  2022-01-22       Impact factor: 3.357

Review 3.  The Trends and Hotspots in Premature Ovarian Insufficiency Therapy from 2000 to 2022.

Authors:  Yan Tong; Nan Cheng; Xinran Jiang; Kai Wang; Fei Wang; Xinxin Lin; Fang Wang
Journal:  Int J Environ Res Public Health       Date:  2022-09-17       Impact factor: 4.614

  3 in total

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