Subsequent menstrual disorder after spontaneous menarche in Turner syndrome
Objective Turner syndrome (TS) is a congenital disease characterized by delayed puberty, ovarian dysgenesis and short stature. Although most patients are diagnosed with primary amenorrhea, approximately 15‐20% of patients with TS are reported to have spontaneous menarche. However, little is known ab...
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Veröffentlicht in: | Clinical endocrinology (Oxford) 2021-07, Vol.95 (1), p.163-168 |
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creator | Komura, Naoko Mabuchi, Seiji Sawada, Kenjiro Nishio, Yukihiro Kimura, Tadashi Komura, Hiroko |
description | Objective
Turner syndrome (TS) is a congenital disease characterized by delayed puberty, ovarian dysgenesis and short stature. Although most patients are diagnosed with primary amenorrhea, approximately 15‐20% of patients with TS are reported to have spontaneous menarche. However, little is known about their menstruation status after spontaneous menarche. In the current study, we investigated the menstrual abnormalities after spontaneous menarche in TS patients.
Design
Retrospective study.
Patients
This study included TS patients with spontaneous menarche at Osaka Police Hospital or Komura Women’s Clinic between April 2015 and December 2019.
Measurements
Data regarding the age of menarche, menstruation status and chromosomal karyotype were collected and retrospectively analyzed.
Results
Of 172 TS patients, 32 with spontaneous menarche were identified. The median age of menarche was 12 years old. Premature ovarian insufficiency (POI) after menarche was observed in 12 patients (37.5%) and the median age at menopause was 20 years old. The average period from spontaneous menarche to menopause in these patients was 5.1 years. Five patients (15.6%) had irregular menstruation and 15 (46.9%) had regular menstruation. When examined according to the structural abnormality of the X chromosome, all patients with structural abnormality of the X chromosome were diagnosed with POI after spontaneous menarche, and none with mosaic without structural abnormality were diagnosed with POI.
Conclusion
Approximately one‐third of TS patients with spontaneous menarche were diagnosed with POI after menarche for an average of 5.1 years. Counseling is required for TS patients and their parents, including information about menstrual abnormalities or fertility preservation. |
doi_str_mv | 10.1111/cen.14449 |
format | Article |
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Turner syndrome (TS) is a congenital disease characterized by delayed puberty, ovarian dysgenesis and short stature. Although most patients are diagnosed with primary amenorrhea, approximately 15‐20% of patients with TS are reported to have spontaneous menarche. However, little is known about their menstruation status after spontaneous menarche. In the current study, we investigated the menstrual abnormalities after spontaneous menarche in TS patients.
Design
Retrospective study.
Patients
This study included TS patients with spontaneous menarche at Osaka Police Hospital or Komura Women’s Clinic between April 2015 and December 2019.
Measurements
Data regarding the age of menarche, menstruation status and chromosomal karyotype were collected and retrospectively analyzed.
Results
Of 172 TS patients, 32 with spontaneous menarche were identified. The median age of menarche was 12 years old. Premature ovarian insufficiency (POI) after menarche was observed in 12 patients (37.5%) and the median age at menopause was 20 years old. The average period from spontaneous menarche to menopause in these patients was 5.1 years. Five patients (15.6%) had irregular menstruation and 15 (46.9%) had regular menstruation. When examined according to the structural abnormality of the X chromosome, all patients with structural abnormality of the X chromosome were diagnosed with POI after spontaneous menarche, and none with mosaic without structural abnormality were diagnosed with POI.
Conclusion
Approximately one‐third of TS patients with spontaneous menarche were diagnosed with POI after menarche for an average of 5.1 years. Counseling is required for TS patients and their parents, including information about menstrual abnormalities or fertility preservation.</description><identifier>ISSN: 0300-0664</identifier><identifier>EISSN: 1365-2265</identifier><identifier>DOI: 10.1111/cen.14449</identifier><identifier>PMID: 33617655</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Age ; Amenorrhea ; Fertility ; Genetic disorders ; karyotype ; Karyotypes ; Menarche ; Menopause ; Menstruation ; Ovaries ; primary ovarian insufficiency ; Puberty ; spontaneous menarche ; Turner syndrome ; Turner's syndrome ; X chromosomes</subject><ispartof>Clinical endocrinology (Oxford), 2021-07, Vol.95 (1), p.163-168</ispartof><rights>2021 John Wiley & Sons Ltd</rights><rights>2021 John Wiley & Sons Ltd.</rights><rights>Copyright © 2021 John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3539-d2f8f161acea98c7f9f33902477c7213bca1a0a64b21f9a719321ee81a8e37b43</citedby><cites>FETCH-LOGICAL-c3539-d2f8f161acea98c7f9f33902477c7213bca1a0a64b21f9a719321ee81a8e37b43</cites><orcidid>0000-0002-8104-750X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fcen.14449$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fcen.14449$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33617655$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Komura, Naoko</creatorcontrib><creatorcontrib>Mabuchi, Seiji</creatorcontrib><creatorcontrib>Sawada, Kenjiro</creatorcontrib><creatorcontrib>Nishio, Yukihiro</creatorcontrib><creatorcontrib>Kimura, Tadashi</creatorcontrib><creatorcontrib>Komura, Hiroko</creatorcontrib><title>Subsequent menstrual disorder after spontaneous menarche in Turner syndrome</title><title>Clinical endocrinology (Oxford)</title><addtitle>Clin Endocrinol (Oxf)</addtitle><description>Objective
Turner syndrome (TS) is a congenital disease characterized by delayed puberty, ovarian dysgenesis and short stature. Although most patients are diagnosed with primary amenorrhea, approximately 15‐20% of patients with TS are reported to have spontaneous menarche. However, little is known about their menstruation status after spontaneous menarche. In the current study, we investigated the menstrual abnormalities after spontaneous menarche in TS patients.
Design
Retrospective study.
Patients
This study included TS patients with spontaneous menarche at Osaka Police Hospital or Komura Women’s Clinic between April 2015 and December 2019.
Measurements
Data regarding the age of menarche, menstruation status and chromosomal karyotype were collected and retrospectively analyzed.
Results
Of 172 TS patients, 32 with spontaneous menarche were identified. The median age of menarche was 12 years old. Premature ovarian insufficiency (POI) after menarche was observed in 12 patients (37.5%) and the median age at menopause was 20 years old. The average period from spontaneous menarche to menopause in these patients was 5.1 years. Five patients (15.6%) had irregular menstruation and 15 (46.9%) had regular menstruation. When examined according to the structural abnormality of the X chromosome, all patients with structural abnormality of the X chromosome were diagnosed with POI after spontaneous menarche, and none with mosaic without structural abnormality were diagnosed with POI.
Conclusion
Approximately one‐third of TS patients with spontaneous menarche were diagnosed with POI after menarche for an average of 5.1 years. Counseling is required for TS patients and their parents, including information about menstrual abnormalities or fertility preservation.</description><subject>Age</subject><subject>Amenorrhea</subject><subject>Fertility</subject><subject>Genetic disorders</subject><subject>karyotype</subject><subject>Karyotypes</subject><subject>Menarche</subject><subject>Menopause</subject><subject>Menstruation</subject><subject>Ovaries</subject><subject>primary ovarian insufficiency</subject><subject>Puberty</subject><subject>spontaneous menarche</subject><subject>Turner syndrome</subject><subject>Turner's syndrome</subject><subject>X chromosomes</subject><issn>0300-0664</issn><issn>1365-2265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp10LtOwzAYBWALgWi5DLwAisQCQ6jvjkdUcRMVDJTZcpw_IlUuxU6E-va4pDAg4cEe_Ono6CB0RvA1iWfmoL0mnHO9h6aESZFSKsU-mmKGcYql5BN0FMIKYywyrA7RhDFJlBRiip5ehzzAxwBtnzTQht4Ptk6KKnS-AJ_Yso93WHdtb1vohrBF1rt3SKo2WQ6-3X5v2sJ3DZygg9LWAU537zF6u7tdzh_Sxcv94_xmkTommE4LWmYlkcQ6sDpzqtQlYxpTrpRTlLDcWWKxlTynpNRWEc0oAciIzYCpnLNjdDnmrn0Xm4feNFVwUNdjRUO5plJijmmkF3_oqoulYztDBZMqOqGjuhqV810IHkqz9lVj_cYQbLYLm7iw-V442vNd4pA3UPzKn0kjmI3gs6ph83-Smd8-j5Ff4KqEsQ</recordid><startdate>202107</startdate><enddate>202107</enddate><creator>Komura, Naoko</creator><creator>Mabuchi, Seiji</creator><creator>Sawada, Kenjiro</creator><creator>Nishio, Yukihiro</creator><creator>Kimura, Tadashi</creator><creator>Komura, Hiroko</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8104-750X</orcidid></search><sort><creationdate>202107</creationdate><title>Subsequent menstrual disorder after spontaneous menarche in Turner syndrome</title><author>Komura, Naoko ; Mabuchi, Seiji ; Sawada, Kenjiro ; Nishio, Yukihiro ; Kimura, Tadashi ; Komura, Hiroko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3539-d2f8f161acea98c7f9f33902477c7213bca1a0a64b21f9a719321ee81a8e37b43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Age</topic><topic>Amenorrhea</topic><topic>Fertility</topic><topic>Genetic disorders</topic><topic>karyotype</topic><topic>Karyotypes</topic><topic>Menarche</topic><topic>Menopause</topic><topic>Menstruation</topic><topic>Ovaries</topic><topic>primary ovarian insufficiency</topic><topic>Puberty</topic><topic>spontaneous menarche</topic><topic>Turner syndrome</topic><topic>Turner's syndrome</topic><topic>X chromosomes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Komura, Naoko</creatorcontrib><creatorcontrib>Mabuchi, Seiji</creatorcontrib><creatorcontrib>Sawada, Kenjiro</creatorcontrib><creatorcontrib>Nishio, Yukihiro</creatorcontrib><creatorcontrib>Kimura, Tadashi</creatorcontrib><creatorcontrib>Komura, Hiroko</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical endocrinology (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Komura, Naoko</au><au>Mabuchi, Seiji</au><au>Sawada, Kenjiro</au><au>Nishio, Yukihiro</au><au>Kimura, Tadashi</au><au>Komura, Hiroko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Subsequent menstrual disorder after spontaneous menarche in Turner syndrome</atitle><jtitle>Clinical endocrinology (Oxford)</jtitle><addtitle>Clin Endocrinol (Oxf)</addtitle><date>2021-07</date><risdate>2021</risdate><volume>95</volume><issue>1</issue><spage>163</spage><epage>168</epage><pages>163-168</pages><issn>0300-0664</issn><eissn>1365-2265</eissn><abstract>Objective
Turner syndrome (TS) is a congenital disease characterized by delayed puberty, ovarian dysgenesis and short stature. Although most patients are diagnosed with primary amenorrhea, approximately 15‐20% of patients with TS are reported to have spontaneous menarche. However, little is known about their menstruation status after spontaneous menarche. In the current study, we investigated the menstrual abnormalities after spontaneous menarche in TS patients.
Design
Retrospective study.
Patients
This study included TS patients with spontaneous menarche at Osaka Police Hospital or Komura Women’s Clinic between April 2015 and December 2019.
Measurements
Data regarding the age of menarche, menstruation status and chromosomal karyotype were collected and retrospectively analyzed.
Results
Of 172 TS patients, 32 with spontaneous menarche were identified. The median age of menarche was 12 years old. Premature ovarian insufficiency (POI) after menarche was observed in 12 patients (37.5%) and the median age at menopause was 20 years old. The average period from spontaneous menarche to menopause in these patients was 5.1 years. Five patients (15.6%) had irregular menstruation and 15 (46.9%) had regular menstruation. When examined according to the structural abnormality of the X chromosome, all patients with structural abnormality of the X chromosome were diagnosed with POI after spontaneous menarche, and none with mosaic without structural abnormality were diagnosed with POI.
Conclusion
Approximately one‐third of TS patients with spontaneous menarche were diagnosed with POI after menarche for an average of 5.1 years. Counseling is required for TS patients and their parents, including information about menstrual abnormalities or fertility preservation.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33617655</pmid><doi>10.1111/cen.14449</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-8104-750X</orcidid></addata></record> |
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source | Wiley Online Library Journals Frontfile Complete |
subjects | Age Amenorrhea Fertility Genetic disorders karyotype Karyotypes Menarche Menopause Menstruation Ovaries primary ovarian insufficiency Puberty spontaneous menarche Turner syndrome Turner's syndrome X chromosomes |
title | Subsequent menstrual disorder after spontaneous menarche in Turner syndrome |
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