GDF15 linked to maternal risk of nausea and vomiting during pregnancy
GDF15, a hormone acting on the brainstem, has been implicated in the nausea and vomiting of pregnancy, including its most severe form, hyperemesis gravidarum (HG), but a full mechanistic understanding is lacking 1 – 4 . Here we report that fetal production of GDF15 and maternal sensitivity to it bot...
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creator | Fejzo, M. Rocha, N. Cimino, I. Lockhart, S. M. Petry, C. J. Kay, R. G. Burling, K. Barker, P. George, A. L. Yasara, N. Premawardhena, A. Gong, S. Cook, E. Rimmington, D. Rainbow, K. Withers, D. J. Cortessis, V. Mullin, P. M. MacGibbon, K. W. Jin, E. Kam, A. Campbell, A. Polasek, O. Tzoneva, G. Gribble, F. M. Yeo, G. S. H. Lam, B. Y. H. Saudek, V. Hughes, I. A. Ong, K. K. Perry, J. R. B. Sutton Cole, A. Baumgarten, M. Welsh, P. Sattar, N. Smith, G. C. S. Charnock-Jones, D. S. Coll, A. P. Meek, C. L. Mettananda, S. Hayward, C. Mancuso, N. O’Rahilly, S. |
description | GDF15, a hormone acting on the brainstem, has been implicated in the nausea and vomiting of pregnancy, including its most severe form, hyperemesis gravidarum (HG), but a full mechanistic understanding is lacking
1
–
4
. Here we report that fetal production of GDF15 and maternal sensitivity to it both contribute substantially to the risk of HG. We confirmed that higher GDF15 levels in maternal blood are associated with vomiting in pregnancy and HG. Using mass spectrometry to detect a naturally labelled GDF15 variant, we demonstrate that the vast majority of GDF15 in the maternal plasma is derived from the feto-placental unit. By studying carriers of rare and common genetic variants, we found that low levels of GDF15 in the non-pregnant state increase the risk of developing HG. Conversely, women with β-thalassaemia, a condition in which GDF15 levels are chronically high
5
, report very low levels of nausea and vomiting of pregnancy. In mice, the acute food intake response to a bolus of GDF15 is influenced bi-directionally by prior levels of circulating GDF15 in a manner suggesting that this system is susceptible to desensitization. Our findings support a putative causal role for fetally derived GDF15 in the nausea and vomiting of human pregnancy, with maternal sensitivity, at least partly determined by prepregnancy exposure to the hormone, being a major influence on its severity. They also suggest mechanism-based approaches to the treatment and prevention of HG.
Elevated circulating levels of GDF15 in pregnant women are associated with severe nausea and vomiting, and sensitivity to such symptoms during pregnancy is partly determined by prepregnancy levels of this hormone. |
doi_str_mv | 10.1038/s41586-023-06921-9 |
format | Article |
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1
–
4
. Here we report that fetal production of GDF15 and maternal sensitivity to it both contribute substantially to the risk of HG. We confirmed that higher GDF15 levels in maternal blood are associated with vomiting in pregnancy and HG. Using mass spectrometry to detect a naturally labelled GDF15 variant, we demonstrate that the vast majority of GDF15 in the maternal plasma is derived from the feto-placental unit. By studying carriers of rare and common genetic variants, we found that low levels of GDF15 in the non-pregnant state increase the risk of developing HG. Conversely, women with β-thalassaemia, a condition in which GDF15 levels are chronically high
5
, report very low levels of nausea and vomiting of pregnancy. In mice, the acute food intake response to a bolus of GDF15 is influenced bi-directionally by prior levels of circulating GDF15 in a manner suggesting that this system is susceptible to desensitization. Our findings support a putative causal role for fetally derived GDF15 in the nausea and vomiting of human pregnancy, with maternal sensitivity, at least partly determined by prepregnancy exposure to the hormone, being a major influence on its severity. They also suggest mechanism-based approaches to the treatment and prevention of HG.
Elevated circulating levels of GDF15 in pregnant women are associated with severe nausea and vomiting, and sensitivity to such symptoms during pregnancy is partly determined by prepregnancy levels of this hormone.</description><identifier>ISSN: 0028-0836</identifier><identifier>ISSN: 1476-4687</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/s41586-023-06921-9</identifier><identifier>PMID: 38092039</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>45 ; 631/208/205 ; 64/60 ; 692/308/575 ; 692/699/2732 ; 82/1 ; 82/58 ; Animals ; beta-Thalassemia - blood ; beta-Thalassemia - metabolism ; Brain stem ; Desensitization ; Female ; Fetus - metabolism ; Fetuses ; Food intake ; Genetic diversity ; Genetic variance ; Growth Differentiation Factor 15 - blood ; Growth Differentiation Factor 15 - metabolism ; Hormones - blood ; Hormones - metabolism ; Humanities and Social Sciences ; Humans ; Hyperemesis Gravidarum - complications ; Hyperemesis Gravidarum - metabolism ; Hyperemesis Gravidarum - prevention & control ; Hyperemesis Gravidarum - therapy ; Mass spectrometry ; Mass spectroscopy ; Mice ; multidisciplinary ; Nausea ; Nausea - blood ; Nausea - complications ; Nausea - metabolism ; Peptides ; Placenta - metabolism ; Pregnancy ; Pregnancy complications ; Risk ; Science ; Science (multidisciplinary) ; Scientific imaging ; Sensitivity ; Thalassemia ; Vomiting ; Vomiting - blood ; Vomiting - complications ; Vomiting - metabolism</subject><ispartof>Nature (London), 2024-01, Vol.625 (7996), p.760-767</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>Copyright Nature Publishing Group Jan 25, 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c541t-be8b01126bf57ef985daa9ad7731dc0f340675d2fa4895f2d8b831e70938c2e63</citedby><cites>FETCH-LOGICAL-c541t-be8b01126bf57ef985daa9ad7731dc0f340675d2fa4895f2d8b831e70938c2e63</cites><orcidid>0000-0001-5796-4423 ; 0000-0002-1480-4849 ; 0000-0003-4689-7530 ; 0000-0001-6800-687X ; 0000-0003-0198-5078 ; 0000-0002-2339-1089 ; 0000-0002-0760-0418 ; 0000-0002-9352-5927 ; 0000-0002-9405-9550 ; 0000-0003-4980-9057 ; 0000-0003-2092-4350 ; 0000-0002-6642-9825 ; 0009-0009-0335-1571 ; 0000-0002-6534-3114 ; 0000-0003-2199-4449 ; 0000-0003-1397-5408 ; 0000-0001-6483-3771 ; 0000-0003-2124-0997 ; 0000-0002-2936-4890 ; 0000-0002-3827-8687 ; 0000-0002-7970-3643 ; 0000-0002-6782-1626 ; 0000-0002-1604-2593</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/s41586-023-06921-9$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/s41586-023-06921-9$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38092039$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fejzo, M.</creatorcontrib><creatorcontrib>Rocha, N.</creatorcontrib><creatorcontrib>Cimino, I.</creatorcontrib><creatorcontrib>Lockhart, S. M.</creatorcontrib><creatorcontrib>Petry, C. J.</creatorcontrib><creatorcontrib>Kay, R. G.</creatorcontrib><creatorcontrib>Burling, K.</creatorcontrib><creatorcontrib>Barker, P.</creatorcontrib><creatorcontrib>George, A. L.</creatorcontrib><creatorcontrib>Yasara, N.</creatorcontrib><creatorcontrib>Premawardhena, A.</creatorcontrib><creatorcontrib>Gong, S.</creatorcontrib><creatorcontrib>Cook, E.</creatorcontrib><creatorcontrib>Rimmington, D.</creatorcontrib><creatorcontrib>Rainbow, K.</creatorcontrib><creatorcontrib>Withers, D. J.</creatorcontrib><creatorcontrib>Cortessis, V.</creatorcontrib><creatorcontrib>Mullin, P. M.</creatorcontrib><creatorcontrib>MacGibbon, K. W.</creatorcontrib><creatorcontrib>Jin, E.</creatorcontrib><creatorcontrib>Kam, A.</creatorcontrib><creatorcontrib>Campbell, A.</creatorcontrib><creatorcontrib>Polasek, O.</creatorcontrib><creatorcontrib>Tzoneva, G.</creatorcontrib><creatorcontrib>Gribble, F. M.</creatorcontrib><creatorcontrib>Yeo, G. S. H.</creatorcontrib><creatorcontrib>Lam, B. Y. H.</creatorcontrib><creatorcontrib>Saudek, V.</creatorcontrib><creatorcontrib>Hughes, I. A.</creatorcontrib><creatorcontrib>Ong, K. K.</creatorcontrib><creatorcontrib>Perry, J. R. B.</creatorcontrib><creatorcontrib>Sutton Cole, A.</creatorcontrib><creatorcontrib>Baumgarten, M.</creatorcontrib><creatorcontrib>Welsh, P.</creatorcontrib><creatorcontrib>Sattar, N.</creatorcontrib><creatorcontrib>Smith, G. C. S.</creatorcontrib><creatorcontrib>Charnock-Jones, D. S.</creatorcontrib><creatorcontrib>Coll, A. P.</creatorcontrib><creatorcontrib>Meek, C. L.</creatorcontrib><creatorcontrib>Mettananda, S.</creatorcontrib><creatorcontrib>Hayward, C.</creatorcontrib><creatorcontrib>Mancuso, N.</creatorcontrib><creatorcontrib>O’Rahilly, S.</creatorcontrib><title>GDF15 linked to maternal risk of nausea and vomiting during pregnancy</title><title>Nature (London)</title><addtitle>Nature</addtitle><addtitle>Nature</addtitle><description>GDF15, a hormone acting on the brainstem, has been implicated in the nausea and vomiting of pregnancy, including its most severe form, hyperemesis gravidarum (HG), but a full mechanistic understanding is lacking
1
–
4
. Here we report that fetal production of GDF15 and maternal sensitivity to it both contribute substantially to the risk of HG. We confirmed that higher GDF15 levels in maternal blood are associated with vomiting in pregnancy and HG. Using mass spectrometry to detect a naturally labelled GDF15 variant, we demonstrate that the vast majority of GDF15 in the maternal plasma is derived from the feto-placental unit. By studying carriers of rare and common genetic variants, we found that low levels of GDF15 in the non-pregnant state increase the risk of developing HG. Conversely, women with β-thalassaemia, a condition in which GDF15 levels are chronically high
5
, report very low levels of nausea and vomiting of pregnancy. In mice, the acute food intake response to a bolus of GDF15 is influenced bi-directionally by prior levels of circulating GDF15 in a manner suggesting that this system is susceptible to desensitization. Our findings support a putative causal role for fetally derived GDF15 in the nausea and vomiting of human pregnancy, with maternal sensitivity, at least partly determined by prepregnancy exposure to the hormone, being a major influence on its severity. They also suggest mechanism-based approaches to the treatment and prevention of HG.
Elevated circulating levels of GDF15 in pregnant women are associated with severe nausea and vomiting, and sensitivity to such symptoms during pregnancy is partly determined by prepregnancy levels of this hormone.</description><subject>45</subject><subject>631/208/205</subject><subject>64/60</subject><subject>692/308/575</subject><subject>692/699/2732</subject><subject>82/1</subject><subject>82/58</subject><subject>Animals</subject><subject>beta-Thalassemia - blood</subject><subject>beta-Thalassemia - metabolism</subject><subject>Brain stem</subject><subject>Desensitization</subject><subject>Female</subject><subject>Fetus - metabolism</subject><subject>Fetuses</subject><subject>Food intake</subject><subject>Genetic diversity</subject><subject>Genetic variance</subject><subject>Growth Differentiation Factor 15 - blood</subject><subject>Growth Differentiation Factor 15 - metabolism</subject><subject>Hormones - blood</subject><subject>Hormones - metabolism</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Hyperemesis Gravidarum - complications</subject><subject>Hyperemesis Gravidarum - metabolism</subject><subject>Hyperemesis Gravidarum - prevention & control</subject><subject>Hyperemesis Gravidarum - therapy</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Mice</subject><subject>multidisciplinary</subject><subject>Nausea</subject><subject>Nausea - blood</subject><subject>Nausea - complications</subject><subject>Nausea - metabolism</subject><subject>Peptides</subject><subject>Placenta - metabolism</subject><subject>Pregnancy</subject><subject>Pregnancy complications</subject><subject>Risk</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Scientific imaging</subject><subject>Sensitivity</subject><subject>Thalassemia</subject><subject>Vomiting</subject><subject>Vomiting - blood</subject><subject>Vomiting - complications</subject><subject>Vomiting - metabolism</subject><issn>0028-0836</issn><issn>1476-4687</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kUtP3TAQRq2qFVwef6CLylI33YSO3_YKId4SEhtYW07s3AYS-9ZOkPj3JL1AH4vKi1n4zOfxHIQ-EzgiwPT3wonQsgLKKpCGksp8QCvClay41OojWgFQXYFmchftlfIAAIIovoN2mQZDgZkVOr88uyAC9118DB6PCQ9uDDm6HueuPOLU4uimEhx20eOnNHRjF9fYT3kpmxzW0cXm-QB9al1fwuFr3Uf3F-d3p1fVze3l9enJTdUITsaqDroGQqisW6FCa7TwzhnnlWLEN9AyDlIJT1vHtREt9brWjAQFhumGBsn20fE2dzPVQ_BNiGN2vd3kbnD52SbX2b9vYvfDrtOTJaDnI9Sc8O01IaefUyijHbrShL53MaSpWGqAGkUFFTP69R_0IU3LahaKGC45F2ym6JZqciolh_Z9GgJ20WS3muysyf7SZM3c9OXPf7y3vHmZAbYFymbZdMi_3_5P7Aub5p0J</recordid><startdate>20240125</startdate><enddate>20240125</enddate><creator>Fejzo, M.</creator><creator>Rocha, N.</creator><creator>Cimino, I.</creator><creator>Lockhart, S. 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M. ; Petry, C. J. ; Kay, R. G. ; Burling, K. ; Barker, P. ; George, A. L. ; Yasara, N. ; Premawardhena, A. ; Gong, S. ; Cook, E. ; Rimmington, D. ; Rainbow, K. ; Withers, D. J. ; Cortessis, V. ; Mullin, P. M. ; MacGibbon, K. W. ; Jin, E. ; Kam, A. ; Campbell, A. ; Polasek, O. ; Tzoneva, G. ; Gribble, F. M. ; Yeo, G. S. H. ; Lam, B. Y. H. ; Saudek, V. ; Hughes, I. A. ; Ong, K. K. ; Perry, J. R. B. ; Sutton Cole, A. ; Baumgarten, M. ; Welsh, P. ; Sattar, N. ; Smith, G. C. S. ; Charnock-Jones, D. S. ; Coll, A. P. ; Meek, C. 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M.</au><au>Petry, C. J.</au><au>Kay, R. G.</au><au>Burling, K.</au><au>Barker, P.</au><au>George, A. L.</au><au>Yasara, N.</au><au>Premawardhena, A.</au><au>Gong, S.</au><au>Cook, E.</au><au>Rimmington, D.</au><au>Rainbow, K.</au><au>Withers, D. J.</au><au>Cortessis, V.</au><au>Mullin, P. M.</au><au>MacGibbon, K. W.</au><au>Jin, E.</au><au>Kam, A.</au><au>Campbell, A.</au><au>Polasek, O.</au><au>Tzoneva, G.</au><au>Gribble, F. M.</au><au>Yeo, G. S. H.</au><au>Lam, B. Y. H.</au><au>Saudek, V.</au><au>Hughes, I. A.</au><au>Ong, K. K.</au><au>Perry, J. R. B.</au><au>Sutton Cole, A.</au><au>Baumgarten, M.</au><au>Welsh, P.</au><au>Sattar, N.</au><au>Smith, G. C. S.</au><au>Charnock-Jones, D. S.</au><au>Coll, A. P.</au><au>Meek, C. L.</au><au>Mettananda, S.</au><au>Hayward, C.</au><au>Mancuso, N.</au><au>O’Rahilly, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GDF15 linked to maternal risk of nausea and vomiting during pregnancy</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><addtitle>Nature</addtitle><date>2024-01-25</date><risdate>2024</risdate><volume>625</volume><issue>7996</issue><spage>760</spage><epage>767</epage><pages>760-767</pages><issn>0028-0836</issn><issn>1476-4687</issn><eissn>1476-4687</eissn><abstract>GDF15, a hormone acting on the brainstem, has been implicated in the nausea and vomiting of pregnancy, including its most severe form, hyperemesis gravidarum (HG), but a full mechanistic understanding is lacking
1
–
4
. Here we report that fetal production of GDF15 and maternal sensitivity to it both contribute substantially to the risk of HG. We confirmed that higher GDF15 levels in maternal blood are associated with vomiting in pregnancy and HG. Using mass spectrometry to detect a naturally labelled GDF15 variant, we demonstrate that the vast majority of GDF15 in the maternal plasma is derived from the feto-placental unit. By studying carriers of rare and common genetic variants, we found that low levels of GDF15 in the non-pregnant state increase the risk of developing HG. Conversely, women with β-thalassaemia, a condition in which GDF15 levels are chronically high
5
, report very low levels of nausea and vomiting of pregnancy. In mice, the acute food intake response to a bolus of GDF15 is influenced bi-directionally by prior levels of circulating GDF15 in a manner suggesting that this system is susceptible to desensitization. Our findings support a putative causal role for fetally derived GDF15 in the nausea and vomiting of human pregnancy, with maternal sensitivity, at least partly determined by prepregnancy exposure to the hormone, being a major influence on its severity. They also suggest mechanism-based approaches to the treatment and prevention of HG.
Elevated circulating levels of GDF15 in pregnant women are associated with severe nausea and vomiting, and sensitivity to such symptoms during pregnancy is partly determined by prepregnancy levels of this hormone.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>38092039</pmid><doi>10.1038/s41586-023-06921-9</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-5796-4423</orcidid><orcidid>https://orcid.org/0000-0002-1480-4849</orcidid><orcidid>https://orcid.org/0000-0003-4689-7530</orcidid><orcidid>https://orcid.org/0000-0001-6800-687X</orcidid><orcidid>https://orcid.org/0000-0003-0198-5078</orcidid><orcidid>https://orcid.org/0000-0002-2339-1089</orcidid><orcidid>https://orcid.org/0000-0002-0760-0418</orcidid><orcidid>https://orcid.org/0000-0002-9352-5927</orcidid><orcidid>https://orcid.org/0000-0002-9405-9550</orcidid><orcidid>https://orcid.org/0000-0003-4980-9057</orcidid><orcidid>https://orcid.org/0000-0003-2092-4350</orcidid><orcidid>https://orcid.org/0000-0002-6642-9825</orcidid><orcidid>https://orcid.org/0009-0009-0335-1571</orcidid><orcidid>https://orcid.org/0000-0002-6534-3114</orcidid><orcidid>https://orcid.org/0000-0003-2199-4449</orcidid><orcidid>https://orcid.org/0000-0003-1397-5408</orcidid><orcidid>https://orcid.org/0000-0001-6483-3771</orcidid><orcidid>https://orcid.org/0000-0003-2124-0997</orcidid><orcidid>https://orcid.org/0000-0002-2936-4890</orcidid><orcidid>https://orcid.org/0000-0002-3827-8687</orcidid><orcidid>https://orcid.org/0000-0002-7970-3643</orcidid><orcidid>https://orcid.org/0000-0002-6782-1626</orcidid><orcidid>https://orcid.org/0000-0002-1604-2593</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0028-0836 |
ispartof | Nature (London), 2024-01, Vol.625 (7996), p.760-767 |
issn | 0028-0836 1476-4687 1476-4687 |
language | eng |
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source | MEDLINE; SpringerLink Journals; Nature Journals Online |
subjects | 45 631/208/205 64/60 692/308/575 692/699/2732 82/1 82/58 Animals beta-Thalassemia - blood beta-Thalassemia - metabolism Brain stem Desensitization Female Fetus - metabolism Fetuses Food intake Genetic diversity Genetic variance Growth Differentiation Factor 15 - blood Growth Differentiation Factor 15 - metabolism Hormones - blood Hormones - metabolism Humanities and Social Sciences Humans Hyperemesis Gravidarum - complications Hyperemesis Gravidarum - metabolism Hyperemesis Gravidarum - prevention & control Hyperemesis Gravidarum - therapy Mass spectrometry Mass spectroscopy Mice multidisciplinary Nausea Nausea - blood Nausea - complications Nausea - metabolism Peptides Placenta - metabolism Pregnancy Pregnancy complications Risk Science Science (multidisciplinary) Scientific imaging Sensitivity Thalassemia Vomiting Vomiting - blood Vomiting - complications Vomiting - metabolism |
title | GDF15 linked to maternal risk of nausea and vomiting during pregnancy |
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