Literature DB >> 27995424

Fragile X premutation in women: recognizing the health challenges beyond primary ovarian insufficiency.

Luis R Hoyos1, Mili Thakur2,3.   

Abstract

Fragile X premutation carriers have 55-200 CGG repeats in the 5' untranslated region of the FMR1 gene. Women with this premutation face many physical and emotional challenges in their life. Approximately 20% of these women will develop fragile X-associated primary ovarian insufficiency (FXPOI). In addition, they suffer from increased rates of menstrual dysfunction, diminished ovarian reserve, reduction in age of menopause, infertility, dizygotic twinning, and risk of having an offspring with a premutation or full mutation. Consequent chronic hypoestrogenism may result in impaired bone health and increased cardiovascular risk. Neuropsychiatric issues include risk of developing fragile X-associated tremor/ataxia syndrome, neuropathy, musculoskeletal problems, increased prevalence of anxiety, depression, and sleep disturbances independent of the stress of raising an offspring with fragile X syndrome and higher risk of postpartum depression. Some studies have reported a higher prevalence of thyroid abnormalities and hypertension in these women. Reproductive health providers play an important role in the health supervision of women with fragile X premutation. Awareness of these risks and correlation of the various manifestations could help in early diagnosis and coordination of care and services for these women and their families. This paper reviews current evidence regarding the possible conditions that may present in women with premutation-sized repeats beyond FXPOI.

Entities:  

Keywords:  Fragile X premutation; Fragile X-associated tremor/ataxia syndrome; Health concerns in fragile X premutation carriers; Premature ovarian insufficiency; Primary ovarian insufficiency

Mesh:

Substances:

Year:  2016        PMID: 27995424      PMCID: PMC5360682          DOI: 10.1007/s10815-016-0854-6

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


  54 in total

1.  Analysis of the molecular parameters that could predict the risk of manifesting premature ovarian failure in female premutation carriers of fragile X syndrome.

Authors:  Maria-Isabel Tejada; Eva García-Alegría; Amaia Bilbao; Cristina Martínez-Bouzas; Elena Beristain; Marisa Poch; Maria A Ramos-Arroyo; Blanca López; Isabel Fernandez Carvajal; Maria-Pilar Ribate; Feliciano Ramos
Journal:  Menopause       Date:  2008 Sep-Oct       Impact factor: 2.953

2.  Testicular and pituitary inclusion formation in fragile X associated tremor/ataxia syndrome.

Authors:  Claudia M Greco; Kultida Soontrapornchai; Juthamas Wirojanan; John E Gould; Paul J Hagerman; Randi J Hagerman
Journal:  J Urol       Date:  2007-04       Impact factor: 7.450

3.  Association of FMR1 repeat size with ovarian dysfunction.

Authors:  A K Sullivan; M Marcus; M P Epstein; E G Allen; A E Anido; J J Paquin; M Yadav-Shah; S L Sherman
Journal:  Hum Reprod       Date:  2004-12-17       Impact factor: 6.918

Review 4.  Understanding the molecular basis of fragile X syndrome.

Authors:  P Jin; S T Warren
Journal:  Hum Mol Genet       Date:  2000-04-12       Impact factor: 6.150

5.  Expanded clinical phenotype of women with the FMR1 premutation.

Authors:  Sarah M Coffey; Kylee Cook; Nicole Tartaglia; Flora Tassone; Danh V Nguyen; Ruiqin Pan; Hannah E Bronsky; Jennifer Yuhas; Mariya Borodyanskaya; Jim Grigsby; Melanie Doerflinger; Paul J Hagerman; Randi J Hagerman
Journal:  Am J Med Genet A       Date:  2008-04-15       Impact factor: 2.802

Review 6.  The fragile-X premutation: a maturing perspective.

Authors:  Paul J Hagerman; Randi J Hagerman
Journal:  Am J Hum Genet       Date:  2004-03-29       Impact factor: 11.025

7.  The effect of CGG repeat number on ovarian response among fragile X premutation carriers undergoing preimplantation genetic diagnosis.

Authors:  Guy Bibi; Mira Malcov; Yaron Yuval; Adi Reches; Dalit Ben-Yosef; Beni Almog; Ami Amit; Foad Azem
Journal:  Fertil Steril       Date:  2009-05-29       Impact factor: 7.329

8.  Examination of reproductive aging milestones among women who carry the FMR1 premutation.

Authors:  E G Allen; A K Sullivan; M Marcus; C Small; C Dominguez; M P Epstein; K Charen; W He; K C Taylor; S L Sherman
Journal:  Hum Reprod       Date:  2007-06-22       Impact factor: 6.918

9.  Fragile X syndrome: diagnostic and carrier testing.

Authors:  Stephanie Sherman; Beth A Pletcher; Deborah A Driscoll
Journal:  Genet Med       Date:  2005-10       Impact factor: 8.822

10.  FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States.

Authors:  Flora Tassone; Ka Pou Iong; Tzu-Han Tong; Joyce Lo; Louise W Gane; Elizabeth Berry-Kravis; Danh Nguyen; Lisa Y Mu; Jennifer Laffin; Don B Bailey; Randi J Hagerman
Journal:  Genome Med       Date:  2012-12-21       Impact factor: 11.117

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  15 in total

1.  Preimplantation genetic diagnosis versus prenatal diagnosis-decision-making among pregnant FMR1 premutation carriers.

Authors:  Lilach Marom Haham; Inbal Avrahami; Noam Domniz; Liat Ries-Levavi; Michal Berkenstadt; Raoul Orvieto; Yoram Cohen; Shai E Elizur
Journal:  J Assist Reprod Genet       Date:  2018-08-22       Impact factor: 3.412

Review 2.  Primary ovarian insufficiency in classic galactosemia: current understanding and future research opportunities.

Authors:  Mili Thakur; Gerald Feldman; Elizabeth E Puscheck
Journal:  J Assist Reprod Genet       Date:  2017-09-20       Impact factor: 3.412

Review 3.  Transplantation of human umbilical cord mesenchymal stem cells to treat premature ovarian failure.

Authors:  Oldouz Shareghi-Oskoue; Leili Aghebati-Maleki; Mehdi Yousefi
Journal:  Stem Cell Res Ther       Date:  2021-08-11       Impact factor: 8.079

4.  Screening for Fragile X Syndrome Among Filipino Children with Autism Spectrum Disorder.

Authors:  Angel Belle C Dy; Lourdes Bernadette S Tanchanco; Jenica Clarisse Y Sy; Myla Dominicina Levantino; Randi J Hagerman
Journal:  J Autism Dev Disord       Date:  2022-08-16

5.  Men with an FMR1 premutation and their health education needs.

Authors:  Matthew B Walsh; Krista Charen; Lisa Shubeck; Allyn McConkie-Rosell; Nadia Ali; Cecelia Bellcross; Stephanie L Sherman
Journal:  J Genet Couns       Date:  2021-03-31       Impact factor: 2.717

6.  A Single Common Assay for Robust and Rapid Fragile X Mental Retardation Syndrome Screening From Dried Blood Spots.

Authors:  Vivienne J Tan; Mulias Lian; Sultana M H Faradz; Tri I Winarni; Samuel S Chong
Journal:  Front Genet       Date:  2018-11-27       Impact factor: 4.599

Review 7.  Molecular Biomarkers in Fragile X Syndrome.

Authors:  Marwa Zafarullah; Flora Tassone
Journal:  Brain Sci       Date:  2019-04-27

8.  The prevalence of CGG repeat expansion mutation in FMR1 gene in the northern Chinese women of reproductive age.

Authors:  Yinan Ma; Xing Wei; Hong Pan; Songtao Wang; Xin Wang; Xiaowei Liu; Liying Zou; Xiaomei Wang; Xiaorong Wang; Hua Yang; Fengying Wang; Kefang Wang; Lifang Sun; Xiaolin Qiao; Yue Yang; Xiuhua Ma; Dandan Liu; Guifeng Ding; Junqi Ma; Xiuli Yang; Sainan Zhu; Yu Qi; Chenghong Yin
Journal:  BMC Med Genet       Date:  2019-05-16       Impact factor: 2.103

9.  Infertility management in primary care.

Authors:  Angela Thable; Elsie Duff; Cheryl Dika
Journal:  Nurse Pract       Date:  2020-05

10.  The significance of FMR1 CGG repeats in Chinese women with premature ovarian insufficiency and diminished ovarian reserve.

Authors:  Ruiyi Tang; Qi Yu
Journal:  Reprod Biol Endocrinol       Date:  2020-08-12       Impact factor: 5.211

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