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effect of pegylated recombinant human leptin (PEG-OB) on weight loss and inflammatory status in obese subjects
OBJECTIVE: To investigate whether weekly subcutaneous administration of 60 mg of long-acting pegylated human leptin (PEG-OB) for 8 weeks was able to influence weight loss, metabolic profile and inflammatory status of obese subjects on a mildly hypoenergetic diet (deficit: 3.2 MJ/day). DESIGN: A pros...
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Published in: | International Journal of Obesity 2002-04, Vol.26 (4), p.504-509 |
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container_title | International Journal of Obesity |
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creator | Hukshorn, C.J Dielen, F.M.H. van Buurman, W.A Westerterp-Plantenga, M.S Campfield, L.A Saris, W.H.M |
description | OBJECTIVE: To investigate whether weekly subcutaneous administration of 60 mg of long-acting pegylated human leptin (PEG-OB) for 8 weeks was able to influence weight loss, metabolic profile and inflammatory status of obese subjects on a mildly hypoenergetic diet (deficit: 3.2 MJ/day). DESIGN: A prospective, randomized, double-blind and placebo-controlled single-center trial. SUBJECTS: Twenty-eight healthy, obese subjects (16 women, 12 men; age 22-65 y; body mass index 27.7-38.7 kg/m2). MEASUREMENTS: Bodyweight, metabolic profile (including lipids), C-reactive protein (CRP) and soluble TNF α-receptor (sTNF-R) 55 and 75 levels. RESULTS: At the end of the study no significant differences in the delta or percentage weight loss between the placebo (n=14) and PEG-OB (n=14) groups was observed. Also the changes in metabolic profile, CRP, sTNF-R55 and R75 concentrations between the two groups after 8 weeks of treatment did not differ. CONCLUSION: Weekly injection of 60 mg PEG-OB did not lead to additional weight loss after 8 weeks of treatment. Furthermore, PEG-OB administration did not affect the changes in metabolic profile and the inflammatory status of obese subjects. |
doi_str_mv | 10.1038/sj.ijo.0801952 |
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DESIGN: A prospective, randomized, double-blind and placebo-controlled single-center trial. SUBJECTS: Twenty-eight healthy, obese subjects (16 women, 12 men; age 22-65 y; body mass index 27.7-38.7 kg/m2). MEASUREMENTS: Bodyweight, metabolic profile (including lipids), C-reactive protein (CRP) and soluble TNF α-receptor (sTNF-R) 55 and 75 levels. RESULTS: At the end of the study no significant differences in the delta or percentage weight loss between the placebo (n=14) and PEG-OB (n=14) groups was observed. Also the changes in metabolic profile, CRP, sTNF-R55 and R75 concentrations between the two groups after 8 weeks of treatment did not differ. CONCLUSION: Weekly injection of 60 mg PEG-OB did not lead to additional weight loss after 8 weeks of treatment. Furthermore, PEG-OB administration did not affect the changes in metabolic profile and the inflammatory status of obese subjects.</description><identifier>ISSN: 0307-0565</identifier><identifier>EISSN: 1476-5497</identifier><identifier>DOI: 10.1038/sj.ijo.0801952</identifier><identifier>CODEN: IJOBDP</identifier><language>eng</language><publisher>Basingstoke: Nature Publishing Group</publisher><subject>Analysis. Health state ; Biological and medical sciences ; Body mass index ; C-reactive protein ; Cytokines ; Diet ; Drug dosages ; Epidemiology ; General aspects ; humans ; leptin ; Lipids ; low calorie diet ; Medical sciences ; men ; Metabolic diseases ; Metabolism ; Nutrition research ; Obesity ; Proteins ; Public health. Hygiene ; Public health. Hygiene-occupational medicine ; subcutaneous injection ; Substance abuse treatment ; Tumor necrosis factor-TNF ; tumor necrosis factors ; Weight control ; weight loss ; women</subject><ispartof>International Journal of Obesity, 2002-04, Vol.26 (4), p.504-509</ispartof><rights>2002 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Apr 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c383t-d7547f5e849b513c5292b891c5610645816cf77ae7ad071e4f5c74be51a316ce3</citedby><cites>FETCH-LOGICAL-c383t-d7547f5e849b513c5292b891c5610645816cf77ae7ad071e4f5c74be51a316ce3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13592893$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Hukshorn, C.J</creatorcontrib><creatorcontrib>Dielen, F.M.H. van</creatorcontrib><creatorcontrib>Buurman, W.A</creatorcontrib><creatorcontrib>Westerterp-Plantenga, M.S</creatorcontrib><creatorcontrib>Campfield, L.A</creatorcontrib><creatorcontrib>Saris, W.H.M</creatorcontrib><title>effect of pegylated recombinant human leptin (PEG-OB) on weight loss and inflammatory status in obese subjects</title><title>International Journal of Obesity</title><description>OBJECTIVE: To investigate whether weekly subcutaneous administration of 60 mg of long-acting pegylated human leptin (PEG-OB) for 8 weeks was able to influence weight loss, metabolic profile and inflammatory status of obese subjects on a mildly hypoenergetic diet (deficit: 3.2 MJ/day). DESIGN: A prospective, randomized, double-blind and placebo-controlled single-center trial. SUBJECTS: Twenty-eight healthy, obese subjects (16 women, 12 men; age 22-65 y; body mass index 27.7-38.7 kg/m2). MEASUREMENTS: Bodyweight, metabolic profile (including lipids), C-reactive protein (CRP) and soluble TNF α-receptor (sTNF-R) 55 and 75 levels. RESULTS: At the end of the study no significant differences in the delta or percentage weight loss between the placebo (n=14) and PEG-OB (n=14) groups was observed. Also the changes in metabolic profile, CRP, sTNF-R55 and R75 concentrations between the two groups after 8 weeks of treatment did not differ. CONCLUSION: Weekly injection of 60 mg PEG-OB did not lead to additional weight loss after 8 weeks of treatment. Furthermore, PEG-OB administration did not affect the changes in metabolic profile and the inflammatory status of obese subjects.</description><subject>Analysis. Health state</subject><subject>Biological and medical sciences</subject><subject>Body mass index</subject><subject>C-reactive protein</subject><subject>Cytokines</subject><subject>Diet</subject><subject>Drug dosages</subject><subject>Epidemiology</subject><subject>General aspects</subject><subject>humans</subject><subject>leptin</subject><subject>Lipids</subject><subject>low calorie diet</subject><subject>Medical sciences</subject><subject>men</subject><subject>Metabolic diseases</subject><subject>Metabolism</subject><subject>Nutrition research</subject><subject>Obesity</subject><subject>Proteins</subject><subject>Public health. Hygiene</subject><subject>Public health. Hygiene-occupational medicine</subject><subject>subcutaneous injection</subject><subject>Substance abuse treatment</subject><subject>Tumor necrosis factor-TNF</subject><subject>tumor necrosis factors</subject><subject>Weight control</subject><subject>weight loss</subject><subject>women</subject><issn>0307-0565</issn><issn>1476-5497</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNpFkEFr3DAQhUVpoNu0114rCoX24M1Isizr2IQ0LQQSSHMWsna0sbGlrSRT9t9XZRd6Gpj53nvMI-QDgy0D0V_laTtOcQs9MC35K7Jhreoa2Wr1mmxAgGpAdvINeZvzBABSAt-QgN6jKzR6esD9cbYFdzShi8swBhsKfVkXG-iMhzIG-uXx9q55uP5KY6B_cNy_FDrHnKkNOzoGP9tlsSWmI83FljXXHY0DZqR5HaYak9-RC2_njO_P85I8f7_9dfOjuX-4-3nz7b5xohel2SnZKi-xb_UgmXCSaz70mjnZMeha2bPOeaUsKrsDxbD10ql2QMmsqCcUl-TTyfeQ4u8VczFTXFOokYYzzbXgABXaniCX6hMJvTmkcbHpaBiYf5WaPJlaqTlXWgWfz642Ozv7ZIMb83-VkJr3WlTu44nzNhq7T5V5fuLAZK1dia4D8RcxBICO</recordid><startdate>20020401</startdate><enddate>20020401</enddate><creator>Hukshorn, C.J</creator><creator>Dielen, F.M.H. van</creator><creator>Buurman, W.A</creator><creator>Westerterp-Plantenga, M.S</creator><creator>Campfield, L.A</creator><creator>Saris, W.H.M</creator><general>Nature Publishing Group</general><general>Nature Publishing</general><scope>FBQ</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T2</scope><scope>7TK</scope><scope>7TS</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope></search><sort><creationdate>20020401</creationdate><title>effect of pegylated recombinant human leptin (PEG-OB) on weight loss and inflammatory status in obese subjects</title><author>Hukshorn, C.J ; Dielen, F.M.H. van ; Buurman, W.A ; Westerterp-Plantenga, M.S ; Campfield, L.A ; Saris, W.H.M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c383t-d7547f5e849b513c5292b891c5610645816cf77ae7ad071e4f5c74be51a316ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Analysis. Health state</topic><topic>Biological and medical sciences</topic><topic>Body mass index</topic><topic>C-reactive protein</topic><topic>Cytokines</topic><topic>Diet</topic><topic>Drug dosages</topic><topic>Epidemiology</topic><topic>General aspects</topic><topic>humans</topic><topic>leptin</topic><topic>Lipids</topic><topic>low calorie diet</topic><topic>Medical sciences</topic><topic>men</topic><topic>Metabolic diseases</topic><topic>Metabolism</topic><topic>Nutrition research</topic><topic>Obesity</topic><topic>Proteins</topic><topic>Public health. Hygiene</topic><topic>Public health. Hygiene-occupational medicine</topic><topic>subcutaneous injection</topic><topic>Substance abuse treatment</topic><topic>Tumor necrosis factor-TNF</topic><topic>tumor necrosis factors</topic><topic>Weight control</topic><topic>weight loss</topic><topic>women</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hukshorn, C.J</creatorcontrib><creatorcontrib>Dielen, F.M.H. van</creatorcontrib><creatorcontrib>Buurman, W.A</creatorcontrib><creatorcontrib>Westerterp-Plantenga, M.S</creatorcontrib><creatorcontrib>Campfield, L.A</creatorcontrib><creatorcontrib>Saris, W.H.M</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>Agricultural Science Collection</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><jtitle>International Journal of Obesity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hukshorn, C.J</au><au>Dielen, F.M.H. van</au><au>Buurman, W.A</au><au>Westerterp-Plantenga, M.S</au><au>Campfield, L.A</au><au>Saris, W.H.M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>effect of pegylated recombinant human leptin (PEG-OB) on weight loss and inflammatory status in obese subjects</atitle><jtitle>International Journal of Obesity</jtitle><date>2002-04-01</date><risdate>2002</risdate><volume>26</volume><issue>4</issue><spage>504</spage><epage>509</epage><pages>504-509</pages><issn>0307-0565</issn><eissn>1476-5497</eissn><coden>IJOBDP</coden><abstract>OBJECTIVE: To investigate whether weekly subcutaneous administration of 60 mg of long-acting pegylated human leptin (PEG-OB) for 8 weeks was able to influence weight loss, metabolic profile and inflammatory status of obese subjects on a mildly hypoenergetic diet (deficit: 3.2 MJ/day). DESIGN: A prospective, randomized, double-blind and placebo-controlled single-center trial. SUBJECTS: Twenty-eight healthy, obese subjects (16 women, 12 men; age 22-65 y; body mass index 27.7-38.7 kg/m2). MEASUREMENTS: Bodyweight, metabolic profile (including lipids), C-reactive protein (CRP) and soluble TNF α-receptor (sTNF-R) 55 and 75 levels. RESULTS: At the end of the study no significant differences in the delta or percentage weight loss between the placebo (n=14) and PEG-OB (n=14) groups was observed. Also the changes in metabolic profile, CRP, sTNF-R55 and R75 concentrations between the two groups after 8 weeks of treatment did not differ. CONCLUSION: Weekly injection of 60 mg PEG-OB did not lead to additional weight loss after 8 weeks of treatment. Furthermore, PEG-OB administration did not affect the changes in metabolic profile and the inflammatory status of obese subjects.</abstract><cop>Basingstoke</cop><pub>Nature Publishing Group</pub><doi>10.1038/sj.ijo.0801952</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis. Health state Biological and medical sciences Body mass index C-reactive protein Cytokines Diet Drug dosages Epidemiology General aspects humans leptin Lipids low calorie diet Medical sciences men Metabolic diseases Metabolism Nutrition research Obesity Proteins Public health. Hygiene Public health. Hygiene-occupational medicine subcutaneous injection Substance abuse treatment Tumor necrosis factor-TNF tumor necrosis factors Weight control weight loss women |
title | effect of pegylated recombinant human leptin (PEG-OB) on weight loss and inflammatory status in obese subjects |
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