Hypothalamic–pituitary–ovarian dysfunction after prepubertal chemotherapy and cranial irradiation for acute leukaemia
BACKGROUND: We assessed adult hypothalamic–pituitary–ovarian function following treatment with chemotherapy and cranial irradiation for childhood acute lymphoblastic leukaemia. METHODS: The patients (n = 12) had median age at diagnosis of 4.7 years, and at assessment of 20.8 years. They collected a...
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Veröffentlicht in: | Human reproduction (Oxford) 2001-09, Vol.16 (9), p.1838-1844 |
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creator | Bath, Louise E. Anderson, Richard A. Critchley, Hilary O.D. Kelnar, Christopher J.H. Wallace, W.Hamish B. |
description | BACKGROUND: We assessed adult hypothalamic–pituitary–ovarian function following treatment with chemotherapy and cranial irradiation for childhood acute lymphoblastic leukaemia. METHODS: The patients (n = 12) had median age at diagnosis of 4.7 years, and at assessment of 20.8 years. They collected a daily urine sample over two to five consecutive menstrual cycles (total of 41 cycles) for analysis of LH and steroid excretion. Blood sampling and ovarian ultrasound examination was performed in the early follicular phase. Sixteen healthy women with regular menstrual cycles were recruited as controls. RESULTS: Urinary LH excretion was significantly lower in patients throughout the cycle, particularly during the LH surge (P < 0.0001). The length of the luteal phase was significantly shorter in patients than in normal controls (12.2 ± 0.3 versus 13.6 ± 0.4 days, P = 0.01) with a high prevalence of short (≤11 days) luteal phases (15/39 cycles). Luteal phase pregnanediol excretion was slightly but not significantly lower. Follicular and luteal phase excretion of oestrone was lower in patients than in controls (P = 0.01). Early follicular phase plasma oestradiol was also lower in the patient group (P = 0.032) although LH, FSH, inhibin A and B concentrations were similar. CONCLUSIONS: These data indicate that treatment for childhood leukaemia results in subtle ovulatory disorder in some patients, probably related to cranial irradiation. Follow-up of these women is required to detect any effect on reproductive potential. |
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METHODS: The patients (n = 12) had median age at diagnosis of 4.7 years, and at assessment of 20.8 years. They collected a daily urine sample over two to five consecutive menstrual cycles (total of 41 cycles) for analysis of LH and steroid excretion. Blood sampling and ovarian ultrasound examination was performed in the early follicular phase. Sixteen healthy women with regular menstrual cycles were recruited as controls. RESULTS: Urinary LH excretion was significantly lower in patients throughout the cycle, particularly during the LH surge (P < 0.0001). The length of the luteal phase was significantly shorter in patients than in normal controls (12.2 ± 0.3 versus 13.6 ± 0.4 days, P = 0.01) with a high prevalence of short (≤11 days) luteal phases (15/39 cycles). Luteal phase pregnanediol excretion was slightly but not significantly lower. Follicular and luteal phase excretion of oestrone was lower in patients than in controls (P = 0.01). Early follicular phase plasma oestradiol was also lower in the patient group (P = 0.032) although LH, FSH, inhibin A and B concentrations were similar. CONCLUSIONS: These data indicate that treatment for childhood leukaemia results in subtle ovulatory disorder in some patients, probably related to cranial irradiation. Follow-up of these women is required to detect any effect on reproductive potential.</description><identifier>ISSN: 0268-1161</identifier><identifier>EISSN: 1460-2350</identifier><identifier>DOI: 10.1093/humrep/16.9.1838</identifier><identifier>PMID: 11527885</identifier><identifier>CODEN: HUREEE</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Acute Disease ; Adult ; Biological and medical sciences ; chemotherapy ; Combined Modality Therapy ; Cranial Irradiation ; Drug toxicity and drugs side effects treatment ; Estradiol - blood ; Estrone - urine ; Female ; Follicular Phase - urine ; Hormones - blood ; Humans ; Hypothalamo-Hypophyseal System - physiopathology ; leukaemia ; Leukemia - drug therapy ; Leukemia - radiotherapy ; Luteal Phase - physiology ; Luteinizing Hormone - urine ; Medical sciences ; Menstrual Cycle - urine ; ovary ; Ovary - physiopathology ; Pharmacology. Drug treatments ; pituitary ; Pregnanediol - urine ; Puberty ; radiotherapy ; Reference Values ; Time Factors ; Toxicity: urogenital system</subject><ispartof>Human reproduction (Oxford), 2001-09, Vol.16 (9), p.1838-1844</ispartof><rights>European Society of Human Reproduction and Embryology 2001</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-20588ecd7f6a882115b4edda2f713a63b89c4566e63eccba7b8a5f6336a14b663</citedby><cites>FETCH-LOGICAL-c441t-20588ecd7f6a882115b4edda2f713a63b89c4566e63eccba7b8a5f6336a14b663</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,1585,27929,27930</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14061067$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11527885$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bath, Louise E.</creatorcontrib><creatorcontrib>Anderson, Richard A.</creatorcontrib><creatorcontrib>Critchley, Hilary O.D.</creatorcontrib><creatorcontrib>Kelnar, Christopher J.H.</creatorcontrib><creatorcontrib>Wallace, W.Hamish B.</creatorcontrib><title>Hypothalamic–pituitary–ovarian dysfunction after prepubertal chemotherapy and cranial irradiation for acute leukaemia</title><title>Human reproduction (Oxford)</title><addtitle>Hum. Reprod</addtitle><addtitle>Hum. Reprod</addtitle><description>BACKGROUND: We assessed adult hypothalamic–pituitary–ovarian function following treatment with chemotherapy and cranial irradiation for childhood acute lymphoblastic leukaemia. METHODS: The patients (n = 12) had median age at diagnosis of 4.7 years, and at assessment of 20.8 years. They collected a daily urine sample over two to five consecutive menstrual cycles (total of 41 cycles) for analysis of LH and steroid excretion. Blood sampling and ovarian ultrasound examination was performed in the early follicular phase. Sixteen healthy women with regular menstrual cycles were recruited as controls. RESULTS: Urinary LH excretion was significantly lower in patients throughout the cycle, particularly during the LH surge (P < 0.0001). The length of the luteal phase was significantly shorter in patients than in normal controls (12.2 ± 0.3 versus 13.6 ± 0.4 days, P = 0.01) with a high prevalence of short (≤11 days) luteal phases (15/39 cycles). Luteal phase pregnanediol excretion was slightly but not significantly lower. Follicular and luteal phase excretion of oestrone was lower in patients than in controls (P = 0.01). Early follicular phase plasma oestradiol was also lower in the patient group (P = 0.032) although LH, FSH, inhibin A and B concentrations were similar. CONCLUSIONS: These data indicate that treatment for childhood leukaemia results in subtle ovulatory disorder in some patients, probably related to cranial irradiation. Follow-up of these women is required to detect any effect on reproductive potential.</description><subject>Acute Disease</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>chemotherapy</subject><subject>Combined Modality Therapy</subject><subject>Cranial Irradiation</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>Estradiol - blood</subject><subject>Estrone - urine</subject><subject>Female</subject><subject>Follicular Phase - urine</subject><subject>Hormones - blood</subject><subject>Humans</subject><subject>Hypothalamo-Hypophyseal System - physiopathology</subject><subject>leukaemia</subject><subject>Leukemia - drug therapy</subject><subject>Leukemia - radiotherapy</subject><subject>Luteal Phase - physiology</subject><subject>Luteinizing Hormone - urine</subject><subject>Medical sciences</subject><subject>Menstrual Cycle - urine</subject><subject>ovary</subject><subject>Ovary - physiopathology</subject><subject>Pharmacology. Drug treatments</subject><subject>pituitary</subject><subject>Pregnanediol - urine</subject><subject>Puberty</subject><subject>radiotherapy</subject><subject>Reference Values</subject><subject>Time Factors</subject><subject>Toxicity: urogenital system</subject><issn>0268-1161</issn><issn>1460-2350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE2LFDEQhoMo7rh69yR90Yv0bNLprs4c3UUdcUAEBdlLqE5XM3H7y3yIffM_-A_9JWbtwb16SkGe963iYeyp4FvBd_LiGAdH84WA7W4rlFT32EaUwPNCVvw-2_ACVC4EiDP2yPuvnKdRwUN2JkRV1EpVG7bsl3kKR-xxsOb3z1-zDdEGdEuap-_oLI5Zu_gujibYacywC-SyOW2NDbmAfWaONKQGcjgvGY5tZhyONn1Y57C1-DfWTS5DEwNlPcUbpMHiY_agw97Tk9N7zj6_ef3pap8fPrx9d_XqkJuyFCEveKUUmbbuAJUq0uVNSW2LRVcLiSAbtTNlBUAgyZgG60Zh1YGUgKJsAOQ5e7H2zm76FskHPVhvqO9xpCl6XQshecWLBPIVNG7y3lGnZ2eHpEILrm9161W3FqB3-lZ3ijw7dcdmoPYucPKbgOcnAL3BvktqjPV3XMlBcKgT93Llpjj_z9p8pa0P9OMfj-5Gp6660vsv1xoOl4frQr7XH-UfXCutAw</recordid><startdate>20010901</startdate><enddate>20010901</enddate><creator>Bath, Louise E.</creator><creator>Anderson, Richard A.</creator><creator>Critchley, Hilary O.D.</creator><creator>Kelnar, Christopher J.H.</creator><creator>Wallace, W.Hamish B.</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>20010901</creationdate><title>Hypothalamic–pituitary–ovarian dysfunction after prepubertal chemotherapy and cranial irradiation for acute leukaemia</title><author>Bath, Louise E. ; Anderson, Richard A. ; Critchley, Hilary O.D. ; Kelnar, Christopher J.H. ; Wallace, W.Hamish B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-20588ecd7f6a882115b4edda2f713a63b89c4566e63eccba7b8a5f6336a14b663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Acute Disease</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>chemotherapy</topic><topic>Combined Modality Therapy</topic><topic>Cranial Irradiation</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>Estradiol - blood</topic><topic>Estrone - urine</topic><topic>Female</topic><topic>Follicular Phase - urine</topic><topic>Hormones - blood</topic><topic>Humans</topic><topic>Hypothalamo-Hypophyseal System - physiopathology</topic><topic>leukaemia</topic><topic>Leukemia - drug therapy</topic><topic>Leukemia - radiotherapy</topic><topic>Luteal Phase - physiology</topic><topic>Luteinizing Hormone - urine</topic><topic>Medical sciences</topic><topic>Menstrual Cycle - urine</topic><topic>ovary</topic><topic>Ovary - physiopathology</topic><topic>Pharmacology. Drug treatments</topic><topic>pituitary</topic><topic>Pregnanediol - urine</topic><topic>Puberty</topic><topic>radiotherapy</topic><topic>Reference Values</topic><topic>Time Factors</topic><topic>Toxicity: urogenital system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bath, Louise E.</creatorcontrib><creatorcontrib>Anderson, Richard A.</creatorcontrib><creatorcontrib>Critchley, Hilary O.D.</creatorcontrib><creatorcontrib>Kelnar, Christopher J.H.</creatorcontrib><creatorcontrib>Wallace, W.Hamish B.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Human reproduction (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bath, Louise E.</au><au>Anderson, Richard A.</au><au>Critchley, Hilary O.D.</au><au>Kelnar, Christopher J.H.</au><au>Wallace, W.Hamish B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hypothalamic–pituitary–ovarian dysfunction after prepubertal chemotherapy and cranial irradiation for acute leukaemia</atitle><jtitle>Human reproduction (Oxford)</jtitle><stitle>Hum. Reprod</stitle><addtitle>Hum. Reprod</addtitle><date>2001-09-01</date><risdate>2001</risdate><volume>16</volume><issue>9</issue><spage>1838</spage><epage>1844</epage><pages>1838-1844</pages><issn>0268-1161</issn><eissn>1460-2350</eissn><coden>HUREEE</coden><abstract>BACKGROUND: We assessed adult hypothalamic–pituitary–ovarian function following treatment with chemotherapy and cranial irradiation for childhood acute lymphoblastic leukaemia. METHODS: The patients (n = 12) had median age at diagnosis of 4.7 years, and at assessment of 20.8 years. They collected a daily urine sample over two to five consecutive menstrual cycles (total of 41 cycles) for analysis of LH and steroid excretion. Blood sampling and ovarian ultrasound examination was performed in the early follicular phase. Sixteen healthy women with regular menstrual cycles were recruited as controls. RESULTS: Urinary LH excretion was significantly lower in patients throughout the cycle, particularly during the LH surge (P < 0.0001). The length of the luteal phase was significantly shorter in patients than in normal controls (12.2 ± 0.3 versus 13.6 ± 0.4 days, P = 0.01) with a high prevalence of short (≤11 days) luteal phases (15/39 cycles). Luteal phase pregnanediol excretion was slightly but not significantly lower. Follicular and luteal phase excretion of oestrone was lower in patients than in controls (P = 0.01). Early follicular phase plasma oestradiol was also lower in the patient group (P = 0.032) although LH, FSH, inhibin A and B concentrations were similar. CONCLUSIONS: These data indicate that treatment for childhood leukaemia results in subtle ovulatory disorder in some patients, probably related to cranial irradiation. Follow-up of these women is required to detect any effect on reproductive potential.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>11527885</pmid><doi>10.1093/humrep/16.9.1838</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acute Disease Adult Biological and medical sciences chemotherapy Combined Modality Therapy Cranial Irradiation Drug toxicity and drugs side effects treatment Estradiol - blood Estrone - urine Female Follicular Phase - urine Hormones - blood Humans Hypothalamo-Hypophyseal System - physiopathology leukaemia Leukemia - drug therapy Leukemia - radiotherapy Luteal Phase - physiology Luteinizing Hormone - urine Medical sciences Menstrual Cycle - urine ovary Ovary - physiopathology Pharmacology. Drug treatments pituitary Pregnanediol - urine Puberty radiotherapy Reference Values Time Factors Toxicity: urogenital system |
title | Hypothalamic–pituitary–ovarian dysfunction after prepubertal chemotherapy and cranial irradiation for acute leukaemia |
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