Mid-Follicular Phase Pulses of Inhibin B Are Absent in Polycystic Ovarian Syndrome and Are Initiated by Successful Laparoscopic Ovarian Diathermy: A Possible Mechanism Regulating Emergence of the Dominant Follicle
The hypothalamic pulse generator of GnRH is recognized to be central to ovulatory function as evidenced by the anovulation of women with hypogonadotrophic hypogonadism due to Kallmann’s syndrome or severe anorexia nervosa. LH is released from the anterior pituitary in pulses, the frequency of which...
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creator | Lockwood, Gillian M Muttukrishna, S Groome, N. P Matthews, D. R Ledger, W. L |
description | The hypothalamic pulse generator of GnRH is recognized to be central to
ovulatory function as evidenced by the anovulation of women with
hypogonadotrophic hypogonadism due to Kallmann’s syndrome or severe
anorexia nervosa. LH is released from the anterior pituitary in pulses,
the frequency of which is closely entrained with those of GnRH. In
contrast, secretion of FSH is influenced by a number of regulatory
molecules, including GnRH, estradiol, inhibin, and activin. The close
temporal relationship between changes in levels of inhibin B and FSH in
the mid-follicular phase suggests that the release of inhibin B by the
preovulatory follicle critically regulates pituitary FSH secretion.
Polycystic ovarian syndrome (PCOS) is one of the most common endocrine
disorders affecting ovulation, and abnormal ovarian morphology as
detected by ultrasonography remains the most sensitive diagnostic
marker for this disorder. The etiology of PCOS is unclear, but its
effective treatment by both anti-estrogens and by exogenous FSH
suggests that a primary disorder of FSH regulation may be central. To
investigate the possible role of inhibin B in the pathology of PCOS,
serum inhibin B levels were measured in 10 women with PCOS on cycle day
5 of a spontaneous or progestrogen-provoked bleed and compared with
levels on cycle day 5 of 10 women with regular ovulatory cycles. The
mean serum inhibin B levels in the PCOS patients were significantly
higher at 248 (±43.4) pg/mL compared with normal controls, 126
(±18.6) pg/mL (P < 0.01). Ten women with
clomiphene resistant PCOS and 5 normal controls consented to undergo
serial blood sampling on cycle day 5. Time Series Analysis using a
Fourier Transformation to analyze the power spectrum of the data
revealed that in normal women there is a distinct periodicity in
inhibin B levels with a clear peak detectable every 60–70 min
(P < 0.05), whereas in women with ovulatory
dysfunction due to PCOS, no such pattern of regular pulsatility was
seen. Four women with PCOS whose anovulation was successfully treated
with laparoscopic ovarian diathermy (LOD) underwent repeat venous
sampling following LOD. Their serum inhibin B levels fell to the upper
limit of the normal range (160± 38.5) pg/mL, and pulsatility was
initiated It is possible that inhibin B pulses are being generated
directly by the ovary in response to pulses of GnRH in the peripheral
circulation, or indirectly in response to FSH pulses arising in the
pituitary. The function of inhibin B |
doi_str_mv | 10.1210/jcem.83.5.4756 |
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ovulatory function as evidenced by the anovulation of women with
hypogonadotrophic hypogonadism due to Kallmann’s syndrome or severe
anorexia nervosa. LH is released from the anterior pituitary in pulses,
the frequency of which is closely entrained with those of GnRH. In
contrast, secretion of FSH is influenced by a number of regulatory
molecules, including GnRH, estradiol, inhibin, and activin. The close
temporal relationship between changes in levels of inhibin B and FSH in
the mid-follicular phase suggests that the release of inhibin B by the
preovulatory follicle critically regulates pituitary FSH secretion.
Polycystic ovarian syndrome (PCOS) is one of the most common endocrine
disorders affecting ovulation, and abnormal ovarian morphology as
detected by ultrasonography remains the most sensitive diagnostic
marker for this disorder. The etiology of PCOS is unclear, but its
effective treatment by both anti-estrogens and by exogenous FSH
suggests that a primary disorder of FSH regulation may be central. To
investigate the possible role of inhibin B in the pathology of PCOS,
serum inhibin B levels were measured in 10 women with PCOS on cycle day
5 of a spontaneous or progestrogen-provoked bleed and compared with
levels on cycle day 5 of 10 women with regular ovulatory cycles. The
mean serum inhibin B levels in the PCOS patients were significantly
higher at 248 (±43.4) pg/mL compared with normal controls, 126
(±18.6) pg/mL (P < 0.01). Ten women with
clomiphene resistant PCOS and 5 normal controls consented to undergo
serial blood sampling on cycle day 5. Time Series Analysis using a
Fourier Transformation to analyze the power spectrum of the data
revealed that in normal women there is a distinct periodicity in
inhibin B levels with a clear peak detectable every 60–70 min
(P < 0.05), whereas in women with ovulatory
dysfunction due to PCOS, no such pattern of regular pulsatility was
seen. Four women with PCOS whose anovulation was successfully treated
with laparoscopic ovarian diathermy (LOD) underwent repeat venous
sampling following LOD. Their serum inhibin B levels fell to the upper
limit of the normal range (160± 38.5) pg/mL, and pulsatility was
initiated It is possible that inhibin B pulses are being generated
directly by the ovary in response to pulses of GnRH in the peripheral
circulation, or indirectly in response to FSH pulses arising in the
pituitary. The function of inhibin B pulses in the mid-follicular phase
of the normal cycle remains to be elucidated, but the absence of the
normal pulsatile pattern in women with PCOS, in conjunction with high
basal levels of inhibin B arising from the multiple small follicles
characteristic of the PCOS ovary, appears to reinforce the development
of a large cohort of small, developmentally arrested, and ultimately
atretic follicles in these patients. Initiation of normal inhibin B
pulsatility by LOD in patients with polycystic ovaries appears to
correlate with the post-operative onset of ovular cycles.</description><identifier>ISSN: 0021-972X</identifier><identifier>EISSN: 1945-7197</identifier><identifier>DOI: 10.1210/jcem.83.5.4756</identifier><identifier>PMID: 9589683</identifier><identifier>CODEN: JCEMAZ</identifier><language>eng</language><publisher>Bethesda, MD: Endocrine Society</publisher><subject>Biological and medical sciences ; Diathermy - methods ; Female ; Female genital diseases ; Follicle Stimulating Hormone - secretion ; Follicular Phase ; Fourier Analysis ; Gynecology. Andrology. Obstetrics ; Humans ; Inhibins - secretion ; Laparoscopy ; Luteinizing Hormone - secretion ; Medical sciences ; Non tumoral diseases ; Ovarian Follicle - physiopathology ; Ovary - physiopathology ; Periodicity ; Polycystic Ovary Syndrome - physiopathology ; Polycystic Ovary Syndrome - therapy</subject><ispartof>The journal of clinical endocrinology and metabolism, 1998-05, Vol.83 (5), p.1730-1735</ispartof><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3656-dd1c88fea33a2eedb99ab5ce24c081def6eeee4435ca88d279eb2a2109ad99843</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2240384$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9589683$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lockwood, Gillian M</creatorcontrib><creatorcontrib>Muttukrishna, S</creatorcontrib><creatorcontrib>Groome, N. P</creatorcontrib><creatorcontrib>Matthews, D. R</creatorcontrib><creatorcontrib>Ledger, W. L</creatorcontrib><title>Mid-Follicular Phase Pulses of Inhibin B Are Absent in Polycystic Ovarian Syndrome and Are Initiated by Successful Laparoscopic Ovarian Diathermy: A Possible Mechanism Regulating Emergence of the Dominant Follicle</title><title>The journal of clinical endocrinology and metabolism</title><addtitle>J Clin Endocrinol Metab</addtitle><description>The hypothalamic pulse generator of GnRH is recognized to be central to
ovulatory function as evidenced by the anovulation of women with
hypogonadotrophic hypogonadism due to Kallmann’s syndrome or severe
anorexia nervosa. LH is released from the anterior pituitary in pulses,
the frequency of which is closely entrained with those of GnRH. In
contrast, secretion of FSH is influenced by a number of regulatory
molecules, including GnRH, estradiol, inhibin, and activin. The close
temporal relationship between changes in levels of inhibin B and FSH in
the mid-follicular phase suggests that the release of inhibin B by the
preovulatory follicle critically regulates pituitary FSH secretion.
Polycystic ovarian syndrome (PCOS) is one of the most common endocrine
disorders affecting ovulation, and abnormal ovarian morphology as
detected by ultrasonography remains the most sensitive diagnostic
marker for this disorder. The etiology of PCOS is unclear, but its
effective treatment by both anti-estrogens and by exogenous FSH
suggests that a primary disorder of FSH regulation may be central. To
investigate the possible role of inhibin B in the pathology of PCOS,
serum inhibin B levels were measured in 10 women with PCOS on cycle day
5 of a spontaneous or progestrogen-provoked bleed and compared with
levels on cycle day 5 of 10 women with regular ovulatory cycles. The
mean serum inhibin B levels in the PCOS patients were significantly
higher at 248 (±43.4) pg/mL compared with normal controls, 126
(±18.6) pg/mL (P < 0.01). Ten women with
clomiphene resistant PCOS and 5 normal controls consented to undergo
serial blood sampling on cycle day 5. Time Series Analysis using a
Fourier Transformation to analyze the power spectrum of the data
revealed that in normal women there is a distinct periodicity in
inhibin B levels with a clear peak detectable every 60–70 min
(P < 0.05), whereas in women with ovulatory
dysfunction due to PCOS, no such pattern of regular pulsatility was
seen. Four women with PCOS whose anovulation was successfully treated
with laparoscopic ovarian diathermy (LOD) underwent repeat venous
sampling following LOD. Their serum inhibin B levels fell to the upper
limit of the normal range (160± 38.5) pg/mL, and pulsatility was
initiated It is possible that inhibin B pulses are being generated
directly by the ovary in response to pulses of GnRH in the peripheral
circulation, or indirectly in response to FSH pulses arising in the
pituitary. The function of inhibin B pulses in the mid-follicular phase
of the normal cycle remains to be elucidated, but the absence of the
normal pulsatile pattern in women with PCOS, in conjunction with high
basal levels of inhibin B arising from the multiple small follicles
characteristic of the PCOS ovary, appears to reinforce the development
of a large cohort of small, developmentally arrested, and ultimately
atretic follicles in these patients. Initiation of normal inhibin B
pulsatility by LOD in patients with polycystic ovaries appears to
correlate with the post-operative onset of ovular cycles.</description><subject>Biological and medical sciences</subject><subject>Diathermy - methods</subject><subject>Female</subject><subject>Female genital diseases</subject><subject>Follicle Stimulating Hormone - secretion</subject><subject>Follicular Phase</subject><subject>Fourier Analysis</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Inhibins - secretion</subject><subject>Laparoscopy</subject><subject>Luteinizing Hormone - secretion</subject><subject>Medical sciences</subject><subject>Non tumoral diseases</subject><subject>Ovarian Follicle - physiopathology</subject><subject>Ovary - physiopathology</subject><subject>Periodicity</subject><subject>Polycystic Ovary Syndrome - physiopathology</subject><subject>Polycystic Ovary Syndrome - therapy</subject><issn>0021-972X</issn><issn>1945-7197</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU2P0zAQhiMEWsrClRuSD4hbShznw-ZW9gMqdbUVCxK3aGJPWleOHewEKT-U_4O7rVZc8MWy5pnx-86bJG9ptqQ5zT4eJPZLzpblsqjL6lmyoKIo05qK-nmyyLKcpqLOf75MXoVwyDJaFCW7SC5EyUXF2SL5c6dVeuuM0XIy4Ml2DwHJdjIBA3EdWdu9brUln8nKI1m1Ae1I4nvrzCznMGpJ7n-D12DJw2yVdz0SsOqRXls9ahhRkXYmD5OUGEI3GbKBAbwL0g3_dF9Hco--nz-RVZwegm4NkjuUe7A69OQb7qLAUdsduenR79BKPAqMTeTa9dpCFHYyYvB18qKDaOHN-b5MftzefL_6mm7uv6yvVptUsqqsUqWo5LxDYAxyRNUKAW0pMS9kxqnCrsJ4ioKVEjhXeS2wzSFuXYASghfsMvlwmjt492vCMDa9DhKNAYtuCk0tOK9oxSK4PIEyGg8eu2bwugc_NzRrjjk2xxwbzpqyOeYYG96dJ09tj-oJPwcX6-_PdQgSTOfBSh2esDwvMvYosDxhaJWTXlscfEyhObjJ27iZ_33_F2uAvWc</recordid><startdate>199805</startdate><enddate>199805</enddate><creator>Lockwood, Gillian M</creator><creator>Muttukrishna, S</creator><creator>Groome, N. P</creator><creator>Matthews, D. R</creator><creator>Ledger, W. L</creator><general>Endocrine Society</general><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>199805</creationdate><title>Mid-Follicular Phase Pulses of Inhibin B Are Absent in Polycystic Ovarian Syndrome and Are Initiated by Successful Laparoscopic Ovarian Diathermy: A Possible Mechanism Regulating Emergence of the Dominant Follicle</title><author>Lockwood, Gillian M ; Muttukrishna, S ; Groome, N. P ; Matthews, D. R ; Ledger, W. L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3656-dd1c88fea33a2eedb99ab5ce24c081def6eeee4435ca88d279eb2a2109ad99843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Biological and medical sciences</topic><topic>Diathermy - methods</topic><topic>Female</topic><topic>Female genital diseases</topic><topic>Follicle Stimulating Hormone - secretion</topic><topic>Follicular Phase</topic><topic>Fourier Analysis</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Inhibins - secretion</topic><topic>Laparoscopy</topic><topic>Luteinizing Hormone - secretion</topic><topic>Medical sciences</topic><topic>Non tumoral diseases</topic><topic>Ovarian Follicle - physiopathology</topic><topic>Ovary - physiopathology</topic><topic>Periodicity</topic><topic>Polycystic Ovary Syndrome - physiopathology</topic><topic>Polycystic Ovary Syndrome - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lockwood, Gillian M</creatorcontrib><creatorcontrib>Muttukrishna, S</creatorcontrib><creatorcontrib>Groome, N. P</creatorcontrib><creatorcontrib>Matthews, D. R</creatorcontrib><creatorcontrib>Ledger, W. L</creatorcontrib><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>The journal of clinical endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lockwood, Gillian M</au><au>Muttukrishna, S</au><au>Groome, N. P</au><au>Matthews, D. R</au><au>Ledger, W. L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mid-Follicular Phase Pulses of Inhibin B Are Absent in Polycystic Ovarian Syndrome and Are Initiated by Successful Laparoscopic Ovarian Diathermy: A Possible Mechanism Regulating Emergence of the Dominant Follicle</atitle><jtitle>The journal of clinical endocrinology and metabolism</jtitle><addtitle>J Clin Endocrinol Metab</addtitle><date>1998-05</date><risdate>1998</risdate><volume>83</volume><issue>5</issue><spage>1730</spage><epage>1735</epage><pages>1730-1735</pages><issn>0021-972X</issn><eissn>1945-7197</eissn><coden>JCEMAZ</coden><abstract>The hypothalamic pulse generator of GnRH is recognized to be central to
ovulatory function as evidenced by the anovulation of women with
hypogonadotrophic hypogonadism due to Kallmann’s syndrome or severe
anorexia nervosa. LH is released from the anterior pituitary in pulses,
the frequency of which is closely entrained with those of GnRH. In
contrast, secretion of FSH is influenced by a number of regulatory
molecules, including GnRH, estradiol, inhibin, and activin. The close
temporal relationship between changes in levels of inhibin B and FSH in
the mid-follicular phase suggests that the release of inhibin B by the
preovulatory follicle critically regulates pituitary FSH secretion.
Polycystic ovarian syndrome (PCOS) is one of the most common endocrine
disorders affecting ovulation, and abnormal ovarian morphology as
detected by ultrasonography remains the most sensitive diagnostic
marker for this disorder. The etiology of PCOS is unclear, but its
effective treatment by both anti-estrogens and by exogenous FSH
suggests that a primary disorder of FSH regulation may be central. To
investigate the possible role of inhibin B in the pathology of PCOS,
serum inhibin B levels were measured in 10 women with PCOS on cycle day
5 of a spontaneous or progestrogen-provoked bleed and compared with
levels on cycle day 5 of 10 women with regular ovulatory cycles. The
mean serum inhibin B levels in the PCOS patients were significantly
higher at 248 (±43.4) pg/mL compared with normal controls, 126
(±18.6) pg/mL (P < 0.01). Ten women with
clomiphene resistant PCOS and 5 normal controls consented to undergo
serial blood sampling on cycle day 5. Time Series Analysis using a
Fourier Transformation to analyze the power spectrum of the data
revealed that in normal women there is a distinct periodicity in
inhibin B levels with a clear peak detectable every 60–70 min
(P < 0.05), whereas in women with ovulatory
dysfunction due to PCOS, no such pattern of regular pulsatility was
seen. Four women with PCOS whose anovulation was successfully treated
with laparoscopic ovarian diathermy (LOD) underwent repeat venous
sampling following LOD. Their serum inhibin B levels fell to the upper
limit of the normal range (160± 38.5) pg/mL, and pulsatility was
initiated It is possible that inhibin B pulses are being generated
directly by the ovary in response to pulses of GnRH in the peripheral
circulation, or indirectly in response to FSH pulses arising in the
pituitary. The function of inhibin B pulses in the mid-follicular phase
of the normal cycle remains to be elucidated, but the absence of the
normal pulsatile pattern in women with PCOS, in conjunction with high
basal levels of inhibin B arising from the multiple small follicles
characteristic of the PCOS ovary, appears to reinforce the development
of a large cohort of small, developmentally arrested, and ultimately
atretic follicles in these patients. Initiation of normal inhibin B
pulsatility by LOD in patients with polycystic ovaries appears to
correlate with the post-operative onset of ovular cycles.</abstract><cop>Bethesda, MD</cop><pub>Endocrine Society</pub><pmid>9589683</pmid><doi>10.1210/jcem.83.5.4756</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals |
subjects | Biological and medical sciences Diathermy - methods Female Female genital diseases Follicle Stimulating Hormone - secretion Follicular Phase Fourier Analysis Gynecology. Andrology. Obstetrics Humans Inhibins - secretion Laparoscopy Luteinizing Hormone - secretion Medical sciences Non tumoral diseases Ovarian Follicle - physiopathology Ovary - physiopathology Periodicity Polycystic Ovary Syndrome - physiopathology Polycystic Ovary Syndrome - therapy |
title | Mid-Follicular Phase Pulses of Inhibin B Are Absent in Polycystic Ovarian Syndrome and Are Initiated by Successful Laparoscopic Ovarian Diathermy: A Possible Mechanism Regulating Emergence of the Dominant Follicle |
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