Weight-loss maintenance is accompanied by interconnected alterations in circulating FGF21-adiponectin-leptin and bioactive sphingolipids
Weight loss is often followed by weight regain. Characterizing endocrine alterations accompanying weight reduction and regain may disentangle the complex biology of weight-loss maintenance. Here, we profile energy-balance-regulating metabokines and sphingolipids in adults with obesity undergoing an...
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creator | Fiorenza, Matteo Checa, Antonio Sandsdal, Rasmus M. Jensen, Simon B.K. Juhl, Christian R. Noer, Mikkel H. Bogh, Nicolai P. Lundgren, Julie R. Janus, Charlotte Stallknecht, Bente M. Holst, Jens Juul Madsbad, Sten Wheelock, Craig E. Torekov, Signe S. |
description | Weight loss is often followed by weight regain. Characterizing endocrine alterations accompanying weight reduction and regain may disentangle the complex biology of weight-loss maintenance. Here, we profile energy-balance-regulating metabokines and sphingolipids in adults with obesity undergoing an initial low-calorie diet-induced weight loss and a subsequent weight-loss maintenance phase with exercise, glucagon-like peptide-1 (GLP-1) analog therapy, both combined, or placebo. We show that circulating growth differentiation factor 15 (GDF15) and C16:0-C18:0 ceramides transiently increase upon initial diet-induced weight loss. Conversely, circulating fibroblast growth factor 21 (FGF21) is downregulated following weight-loss maintenance with combined exercise and GLP-1 analog therapy, coinciding with increased adiponectin, decreased leptin, and overall decrements in ceramide and sphingosine-1-phosphate levels. Subgroup analyses reveal differential alterations in FGF21-adiponectin-leptin-sphingolipids between weight maintainers and regainers. Clinically, cardiometabolic health outcomes associate with selective metabokine-sphingolipid remodeling signatures. Collectively, our findings indicate distinct FGF21, GDF15, and ceramide responses to diverse phases of weight change and suggest that weight-loss maintenance involves alterations within the metabokine-sphingolipid axis.
[Display omitted]
•Diet-induced weight loss (WL) transiently increases GDF15 and C16:0-C18:0 ceramides•Sustained WL leads to reduced FGF21, leptin, ceramides, and S1P and increased adiponectin•Weight maintainers and regainers exhibit distinct metabokine-sphingolipid alterations•Clinically, these alterations associate with changes in cardiometabolic health outcomes
Fiorenza et al. reveal selective and dynamic alterations in energy-balance-regulating metabokines and sphingolipids throughout weight loss, weight-loss maintenance, and weight regain in adults with obesity. Weight-loss maintenance elicits distinct remodeling patterns within the FGF21-adiponectin-leptin-sphingolipid axis as compared with weight regain, and these changes are associated with cardiometabolic health outcomes. |
doi_str_mv | 10.1016/j.xcrm.2024.101629 |
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[Display omitted]
•Diet-induced weight loss (WL) transiently increases GDF15 and C16:0-C18:0 ceramides•Sustained WL leads to reduced FGF21, leptin, ceramides, and S1P and increased adiponectin•Weight maintainers and regainers exhibit distinct metabokine-sphingolipid alterations•Clinically, these alterations associate with changes in cardiometabolic health outcomes
Fiorenza et al. reveal selective and dynamic alterations in energy-balance-regulating metabokines and sphingolipids throughout weight loss, weight-loss maintenance, and weight regain in adults with obesity. Weight-loss maintenance elicits distinct remodeling patterns within the FGF21-adiponectin-leptin-sphingolipid axis as compared with weight regain, and these changes are associated with cardiometabolic health outcomes.</description><identifier>ISSN: 2666-3791</identifier><identifier>EISSN: 2666-3791</identifier><identifier>DOI: 10.1016/j.xcrm.2024.101629</identifier><identifier>PMID: 38959886</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>adiponectin ; Adiponectin - blood ; Adiponectin - metabolism ; Adult ; ceramide ; Ceramides - blood ; Ceramides - metabolism ; cytokines ; exercise ; Female ; FGF21 ; Fibroblast Growth Factors - blood ; Fibroblast Growth Factors - metabolism ; GDF15 ; GLP-1 receptor agonist ; Growth Differentiation Factor 15 - blood ; Growth Differentiation Factor 15 - metabolism ; Humans ; leptin ; Leptin - blood ; Leptin - metabolism ; Male ; Middle Aged ; obesity ; Obesity - blood ; Obesity - metabolism ; sphingolipids ; Sphingolipids - blood ; Sphingolipids - metabolism ; Weight Loss</subject><ispartof>Cell reports. Medicine, 2024-07, Vol.5 (7), p.101629, Article 101629</ispartof><rights>2024 The Authors</rights><rights>Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.</rights><rights>2024 The Authors 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c445t-63cf9dd0c3ecf670bc9cb53b03bd54fe844066dff2d65662be159c38b5c5e04c3</cites><orcidid>0000-0001-6779-0252</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11293340/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11293340/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,550,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38959886$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:159101966$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Fiorenza, Matteo</creatorcontrib><creatorcontrib>Checa, Antonio</creatorcontrib><creatorcontrib>Sandsdal, Rasmus M.</creatorcontrib><creatorcontrib>Jensen, Simon B.K.</creatorcontrib><creatorcontrib>Juhl, Christian R.</creatorcontrib><creatorcontrib>Noer, Mikkel H.</creatorcontrib><creatorcontrib>Bogh, Nicolai P.</creatorcontrib><creatorcontrib>Lundgren, Julie R.</creatorcontrib><creatorcontrib>Janus, Charlotte</creatorcontrib><creatorcontrib>Stallknecht, Bente M.</creatorcontrib><creatorcontrib>Holst, Jens Juul</creatorcontrib><creatorcontrib>Madsbad, Sten</creatorcontrib><creatorcontrib>Wheelock, Craig E.</creatorcontrib><creatorcontrib>Torekov, Signe S.</creatorcontrib><title>Weight-loss maintenance is accompanied by interconnected alterations in circulating FGF21-adiponectin-leptin and bioactive sphingolipids</title><title>Cell reports. Medicine</title><addtitle>Cell Rep Med</addtitle><description>Weight loss is often followed by weight regain. Characterizing endocrine alterations accompanying weight reduction and regain may disentangle the complex biology of weight-loss maintenance. Here, we profile energy-balance-regulating metabokines and sphingolipids in adults with obesity undergoing an initial low-calorie diet-induced weight loss and a subsequent weight-loss maintenance phase with exercise, glucagon-like peptide-1 (GLP-1) analog therapy, both combined, or placebo. We show that circulating growth differentiation factor 15 (GDF15) and C16:0-C18:0 ceramides transiently increase upon initial diet-induced weight loss. Conversely, circulating fibroblast growth factor 21 (FGF21) is downregulated following weight-loss maintenance with combined exercise and GLP-1 analog therapy, coinciding with increased adiponectin, decreased leptin, and overall decrements in ceramide and sphingosine-1-phosphate levels. Subgroup analyses reveal differential alterations in FGF21-adiponectin-leptin-sphingolipids between weight maintainers and regainers. Clinically, cardiometabolic health outcomes associate with selective metabokine-sphingolipid remodeling signatures. Collectively, our findings indicate distinct FGF21, GDF15, and ceramide responses to diverse phases of weight change and suggest that weight-loss maintenance involves alterations within the metabokine-sphingolipid axis.
[Display omitted]
•Diet-induced weight loss (WL) transiently increases GDF15 and C16:0-C18:0 ceramides•Sustained WL leads to reduced FGF21, leptin, ceramides, and S1P and increased adiponectin•Weight maintainers and regainers exhibit distinct metabokine-sphingolipid alterations•Clinically, these alterations associate with changes in cardiometabolic health outcomes
Fiorenza et al. reveal selective and dynamic alterations in energy-balance-regulating metabokines and sphingolipids throughout weight loss, weight-loss maintenance, and weight regain in adults with obesity. Weight-loss maintenance elicits distinct remodeling patterns within the FGF21-adiponectin-leptin-sphingolipid axis as compared with weight regain, and these changes are associated with cardiometabolic health outcomes.</description><subject>adiponectin</subject><subject>Adiponectin - blood</subject><subject>Adiponectin - metabolism</subject><subject>Adult</subject><subject>ceramide</subject><subject>Ceramides - blood</subject><subject>Ceramides - metabolism</subject><subject>cytokines</subject><subject>exercise</subject><subject>Female</subject><subject>FGF21</subject><subject>Fibroblast Growth Factors - blood</subject><subject>Fibroblast Growth Factors - metabolism</subject><subject>GDF15</subject><subject>GLP-1 receptor agonist</subject><subject>Growth Differentiation Factor 15 - blood</subject><subject>Growth Differentiation Factor 15 - metabolism</subject><subject>Humans</subject><subject>leptin</subject><subject>Leptin - blood</subject><subject>Leptin - metabolism</subject><subject>Male</subject><subject>Middle Aged</subject><subject>obesity</subject><subject>Obesity - blood</subject><subject>Obesity - metabolism</subject><subject>sphingolipids</subject><subject>Sphingolipids - blood</subject><subject>Sphingolipids - metabolism</subject><subject>Weight Loss</subject><issn>2666-3791</issn><issn>2666-3791</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>D8T</sourceid><recordid>eNp9UU1v1DAQjRCIVqV_gAPKkUu2_kicREJCqGJLpUpcQBwtZzzZ9ZLYwc4u9B_ws5mwS9VeuHhm3nvzbPll2WvOVpxxdbVb_YI4rgQT5V9AtM-yc6GUKmTd8ueP-rPsMqUdY0xUnDeSvczOZNNWbdOo8-z3N3Sb7VwMIaV8NM7P6I0HzF3KDUAYJ-Md2ry7zxcuQvAeYSbEDDSa2QWfiMrBRdgPNPtNvr5ZC14Y66awiJ0vBpyo5MaTkwuGsAPmadqSOgxucja9yl70Zkh4eaoX2df1xy_Xn4q7zze31x_uCijLai6UhL61loFE6FXNOmihq2THZGerssemLJlStu-FVZVSokNetSCbroIKWQnyIiuOvuknTvtOT9GNJt7rYJw-Qd-pQ93UpWpr0r8_6okZ0QL6OZrhydpTxrut3oSD5ly0UpaMHN6eHGL4scc069ElwGEwHsM-acnqqmacTpKKoxQi5RGxf7iHM72krHd6iV0vsetj7LT05vELH1b-hUyCd0cB0r8eHEadwCGFbF2keLQN7n_-fwDovsPy</recordid><startdate>20240716</startdate><enddate>20240716</enddate><creator>Fiorenza, Matteo</creator><creator>Checa, Antonio</creator><creator>Sandsdal, Rasmus M.</creator><creator>Jensen, Simon B.K.</creator><creator>Juhl, Christian R.</creator><creator>Noer, Mikkel H.</creator><creator>Bogh, Nicolai P.</creator><creator>Lundgren, Julie R.</creator><creator>Janus, Charlotte</creator><creator>Stallknecht, Bente M.</creator><creator>Holst, Jens Juul</creator><creator>Madsbad, Sten</creator><creator>Wheelock, Craig E.</creator><creator>Torekov, Signe S.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</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><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>ZZAVC</scope><orcidid>https://orcid.org/0000-0001-6779-0252</orcidid></search><sort><creationdate>20240716</creationdate><title>Weight-loss maintenance is accompanied by interconnected alterations in circulating FGF21-adiponectin-leptin and bioactive sphingolipids</title><author>Fiorenza, Matteo ; Checa, Antonio ; Sandsdal, Rasmus M. ; Jensen, Simon B.K. ; Juhl, Christian R. ; Noer, Mikkel H. ; Bogh, Nicolai P. ; Lundgren, Julie R. ; Janus, Charlotte ; Stallknecht, Bente M. ; Holst, Jens Juul ; Madsbad, Sten ; Wheelock, Craig E. ; Torekov, Signe S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c445t-63cf9dd0c3ecf670bc9cb53b03bd54fe844066dff2d65662be159c38b5c5e04c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>adiponectin</topic><topic>Adiponectin - blood</topic><topic>Adiponectin - metabolism</topic><topic>Adult</topic><topic>ceramide</topic><topic>Ceramides - blood</topic><topic>Ceramides - metabolism</topic><topic>cytokines</topic><topic>exercise</topic><topic>Female</topic><topic>FGF21</topic><topic>Fibroblast Growth Factors - blood</topic><topic>Fibroblast Growth Factors - metabolism</topic><topic>GDF15</topic><topic>GLP-1 receptor agonist</topic><topic>Growth Differentiation Factor 15 - blood</topic><topic>Growth Differentiation Factor 15 - metabolism</topic><topic>Humans</topic><topic>leptin</topic><topic>Leptin - blood</topic><topic>Leptin - metabolism</topic><topic>Male</topic><topic>Middle Aged</topic><topic>obesity</topic><topic>Obesity - blood</topic><topic>Obesity - metabolism</topic><topic>sphingolipids</topic><topic>Sphingolipids - blood</topic><topic>Sphingolipids - metabolism</topic><topic>Weight Loss</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fiorenza, Matteo</creatorcontrib><creatorcontrib>Checa, Antonio</creatorcontrib><creatorcontrib>Sandsdal, Rasmus M.</creatorcontrib><creatorcontrib>Jensen, Simon B.K.</creatorcontrib><creatorcontrib>Juhl, Christian R.</creatorcontrib><creatorcontrib>Noer, Mikkel H.</creatorcontrib><creatorcontrib>Bogh, Nicolai P.</creatorcontrib><creatorcontrib>Lundgren, Julie R.</creatorcontrib><creatorcontrib>Janus, Charlotte</creatorcontrib><creatorcontrib>Stallknecht, Bente M.</creatorcontrib><creatorcontrib>Holst, Jens Juul</creatorcontrib><creatorcontrib>Madsbad, Sten</creatorcontrib><creatorcontrib>Wheelock, Craig E.</creatorcontrib><creatorcontrib>Torekov, Signe S.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>Cell reports. Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fiorenza, Matteo</au><au>Checa, Antonio</au><au>Sandsdal, Rasmus M.</au><au>Jensen, Simon B.K.</au><au>Juhl, Christian R.</au><au>Noer, Mikkel H.</au><au>Bogh, Nicolai P.</au><au>Lundgren, Julie R.</au><au>Janus, Charlotte</au><au>Stallknecht, Bente M.</au><au>Holst, Jens Juul</au><au>Madsbad, Sten</au><au>Wheelock, Craig E.</au><au>Torekov, Signe S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Weight-loss maintenance is accompanied by interconnected alterations in circulating FGF21-adiponectin-leptin and bioactive sphingolipids</atitle><jtitle>Cell reports. Medicine</jtitle><addtitle>Cell Rep Med</addtitle><date>2024-07-16</date><risdate>2024</risdate><volume>5</volume><issue>7</issue><spage>101629</spage><pages>101629-</pages><artnum>101629</artnum><issn>2666-3791</issn><eissn>2666-3791</eissn><abstract>Weight loss is often followed by weight regain. Characterizing endocrine alterations accompanying weight reduction and regain may disentangle the complex biology of weight-loss maintenance. Here, we profile energy-balance-regulating metabokines and sphingolipids in adults with obesity undergoing an initial low-calorie diet-induced weight loss and a subsequent weight-loss maintenance phase with exercise, glucagon-like peptide-1 (GLP-1) analog therapy, both combined, or placebo. We show that circulating growth differentiation factor 15 (GDF15) and C16:0-C18:0 ceramides transiently increase upon initial diet-induced weight loss. Conversely, circulating fibroblast growth factor 21 (FGF21) is downregulated following weight-loss maintenance with combined exercise and GLP-1 analog therapy, coinciding with increased adiponectin, decreased leptin, and overall decrements in ceramide and sphingosine-1-phosphate levels. Subgroup analyses reveal differential alterations in FGF21-adiponectin-leptin-sphingolipids between weight maintainers and regainers. Clinically, cardiometabolic health outcomes associate with selective metabokine-sphingolipid remodeling signatures. Collectively, our findings indicate distinct FGF21, GDF15, and ceramide responses to diverse phases of weight change and suggest that weight-loss maintenance involves alterations within the metabokine-sphingolipid axis.
[Display omitted]
•Diet-induced weight loss (WL) transiently increases GDF15 and C16:0-C18:0 ceramides•Sustained WL leads to reduced FGF21, leptin, ceramides, and S1P and increased adiponectin•Weight maintainers and regainers exhibit distinct metabokine-sphingolipid alterations•Clinically, these alterations associate with changes in cardiometabolic health outcomes
Fiorenza et al. reveal selective and dynamic alterations in energy-balance-regulating metabokines and sphingolipids throughout weight loss, weight-loss maintenance, and weight regain in adults with obesity. Weight-loss maintenance elicits distinct remodeling patterns within the FGF21-adiponectin-leptin-sphingolipid axis as compared with weight regain, and these changes are associated with cardiometabolic health outcomes.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>38959886</pmid><doi>10.1016/j.xcrm.2024.101629</doi><orcidid>https://orcid.org/0000-0001-6779-0252</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | adiponectin Adiponectin - blood Adiponectin - metabolism Adult ceramide Ceramides - blood Ceramides - metabolism cytokines exercise Female FGF21 Fibroblast Growth Factors - blood Fibroblast Growth Factors - metabolism GDF15 GLP-1 receptor agonist Growth Differentiation Factor 15 - blood Growth Differentiation Factor 15 - metabolism Humans leptin Leptin - blood Leptin - metabolism Male Middle Aged obesity Obesity - blood Obesity - metabolism sphingolipids Sphingolipids - blood Sphingolipids - metabolism Weight Loss |
title | Weight-loss maintenance is accompanied by interconnected alterations in circulating FGF21-adiponectin-leptin and bioactive sphingolipids |
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