The relationship of sterol regulatory element–binding protein cleavage–activation protein and apolipoprotein E gene polymorphisms with metabolic changes during weight reduction
Abstract Sterol regulatory element–binding protein cleavage–activating protein (SCAP) and apolipoprotein E (apo E) regulate cellular and plasma lipid metabolism. Therefore, variations in the corresponding genes might influence weight reduction and obesity-associated metabolic changes. We investigate...
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Veröffentlicht in: | Metabolism, clinical and experimental clinical and experimental, 2007-07, Vol.56 (7), p.876-880 |
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creator | Nieminen, Tuomo Matinheikki, Jussi Nenonen, Arja Kukkonen-Harjula, Katriina Lindi, Virpi Hämelahti, Päivi Laaksonen, Reijo Fan, Yue-Mei Kähönen, Mika Fogelholm, Mikael Lehtimäki, Terho |
description | Abstract Sterol regulatory element–binding protein cleavage–activating protein (SCAP) and apolipoprotein E (apo E) regulate cellular and plasma lipid metabolism. Therefore, variations in the corresponding genes might influence weight reduction and obesity-associated metabolic changes. We investigated the relationships of SCAP (Ile796Val) and apo E polymorphisms on metabolic changes during weight reduction by using a 12-week very low-energy diet. Body composition, serum lipids, plasma glucose, and insulin were assessed in 78 healthy premenopausal women (initial body mass index, 34 ± 4 kg/m2 ; age, 40 ± 4 years) before and after the intervention. The SCAP genotype groups did not differ in the responses of any parameters measured during weight reduction. Apo E did not differentiate the weight loss, but the changes in total and low-density lipoprotein cholesterol for the genotype groups apo E ε 2/3, ε 3/3, as well as ε 3/4 and ε 4/4 combined were −0.94 ± 0.56 and −0.59 ± 0.32, −0.71 ± 0.49 and −0.49 ± 0.45, and −0.55 ± 0.47 and −0.37 ± 0.39 mmol/L, respectively ( P < .05 for both). In conclusion, neither the SCAP Ile796Val nor the apo E polymorphism was associated with weight loss in obese premenopausal women. However, the apo E—but not SCAP genotype—seems to be one of the modifying factors for serum cholesterol concentrations during very low-energy diet in obese premenopausal women. |
doi_str_mv | 10.1016/j.metabol.2007.02.003 |
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Therefore, variations in the corresponding genes might influence weight reduction and obesity-associated metabolic changes. We investigated the relationships of SCAP (Ile796Val) and apo E polymorphisms on metabolic changes during weight reduction by using a 12-week very low-energy diet. Body composition, serum lipids, plasma glucose, and insulin were assessed in 78 healthy premenopausal women (initial body mass index, 34 ± 4 kg/m2 ; age, 40 ± 4 years) before and after the intervention. The SCAP genotype groups did not differ in the responses of any parameters measured during weight reduction. Apo E did not differentiate the weight loss, but the changes in total and low-density lipoprotein cholesterol for the genotype groups apo E ε 2/3, ε 3/3, as well as ε 3/4 and ε 4/4 combined were −0.94 ± 0.56 and −0.59 ± 0.32, −0.71 ± 0.49 and −0.49 ± 0.45, and −0.55 ± 0.47 and −0.37 ± 0.39 mmol/L, respectively ( P < .05 for both). In conclusion, neither the SCAP Ile796Val nor the apo E polymorphism was associated with weight loss in obese premenopausal women. However, the apo E—but not SCAP genotype—seems to be one of the modifying factors for serum cholesterol concentrations during very low-energy diet in obese premenopausal women.</description><identifier>ISSN: 0026-0495</identifier><identifier>EISSN: 1532-8600</identifier><identifier>DOI: 10.1016/j.metabol.2007.02.003</identifier><identifier>PMID: 17570245</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adult ; Apolipoproteins E - genetics ; Biological and medical sciences ; Caloric Restriction ; Cholesterol - blood ; Cholesterol, LDL - blood ; Endocrinology & Metabolism ; Female ; Humans ; Intracellular Signaling Peptides and Proteins - genetics ; Medical sciences ; Membrane Proteins - genetics ; Metabolic diseases ; Middle Aged ; Polymorphism, Genetic ; Weight Loss - physiology</subject><ispartof>Metabolism, clinical and experimental, 2007-07, Vol.56 (7), p.876-880</ispartof><rights>Elsevier Inc.</rights><rights>2007 Elsevier Inc.</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-fc61105611b27ca1f5b73b6e98700e8be705b429562820b9f9845ec1175994893</citedby><cites>FETCH-LOGICAL-c448t-fc61105611b27ca1f5b73b6e98700e8be705b429562820b9f9845ec1175994893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.metabol.2007.02.003$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18903500$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17570245$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nieminen, Tuomo</creatorcontrib><creatorcontrib>Matinheikki, Jussi</creatorcontrib><creatorcontrib>Nenonen, Arja</creatorcontrib><creatorcontrib>Kukkonen-Harjula, Katriina</creatorcontrib><creatorcontrib>Lindi, Virpi</creatorcontrib><creatorcontrib>Hämelahti, Päivi</creatorcontrib><creatorcontrib>Laaksonen, Reijo</creatorcontrib><creatorcontrib>Fan, Yue-Mei</creatorcontrib><creatorcontrib>Kähönen, Mika</creatorcontrib><creatorcontrib>Fogelholm, Mikael</creatorcontrib><creatorcontrib>Lehtimäki, Terho</creatorcontrib><title>The relationship of sterol regulatory element–binding protein cleavage–activation protein and apolipoprotein E gene polymorphisms with metabolic changes during weight reduction</title><title>Metabolism, clinical and experimental</title><addtitle>Metabolism</addtitle><description>Abstract Sterol regulatory element–binding protein cleavage–activating protein (SCAP) and apolipoprotein E (apo E) regulate cellular and plasma lipid metabolism. Therefore, variations in the corresponding genes might influence weight reduction and obesity-associated metabolic changes. We investigated the relationships of SCAP (Ile796Val) and apo E polymorphisms on metabolic changes during weight reduction by using a 12-week very low-energy diet. Body composition, serum lipids, plasma glucose, and insulin were assessed in 78 healthy premenopausal women (initial body mass index, 34 ± 4 kg/m2 ; age, 40 ± 4 years) before and after the intervention. The SCAP genotype groups did not differ in the responses of any parameters measured during weight reduction. Apo E did not differentiate the weight loss, but the changes in total and low-density lipoprotein cholesterol for the genotype groups apo E ε 2/3, ε 3/3, as well as ε 3/4 and ε 4/4 combined were −0.94 ± 0.56 and −0.59 ± 0.32, −0.71 ± 0.49 and −0.49 ± 0.45, and −0.55 ± 0.47 and −0.37 ± 0.39 mmol/L, respectively ( P < .05 for both). In conclusion, neither the SCAP Ile796Val nor the apo E polymorphism was associated with weight loss in obese premenopausal women. However, the apo E—but not SCAP genotype—seems to be one of the modifying factors for serum cholesterol concentrations during very low-energy diet in obese premenopausal women.</description><subject>Adult</subject><subject>Apolipoproteins E - genetics</subject><subject>Biological and medical sciences</subject><subject>Caloric Restriction</subject><subject>Cholesterol - blood</subject><subject>Cholesterol, LDL - blood</subject><subject>Endocrinology & Metabolism</subject><subject>Female</subject><subject>Humans</subject><subject>Intracellular Signaling Peptides and Proteins - genetics</subject><subject>Medical sciences</subject><subject>Membrane Proteins - genetics</subject><subject>Metabolic diseases</subject><subject>Middle Aged</subject><subject>Polymorphism, Genetic</subject><subject>Weight Loss - physiology</subject><issn>0026-0495</issn><issn>1532-8600</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUkuO1DAQtRCIGRqOAPIGdt2UnTifDWg0Gj7SSCwYJHaW41QSN4kd7KRHveMOXIUTcRIcOjASGza2VPXqVdV7RchTBjsGLHu53w04qcr1Ow6Q74DvAJJ75JyJhG-LDOA-OQfg2RbSUpyRRyHsIQLzIntIzlgucuCpOCc_bjqkHns1GWdDZ0bqGhom9K6P4XaOCeePFHsc0E4_v32vjK2Nbeno3YTGUt2jOqgWY0rpyRx-E_3NKltTNbrejO5P6Iq2aJHG4HFwfuxMGAK9NVNH14WMprpTtsVA69kvvW7RtN0U56lnvdA_Jg8a1Qd8sv4b8unN1c3lu-31h7fvLy-utzpNi2nb6IwxEPGpeK4Va0SVJ1WGZZEDYFFhDqJKeSkyXnCoyqYsUoGaRXXKMi3KZENenHjj7F9nDJMcTNDY98qim4PkbBEx4REoTkDtXQgeGzl6Myh_lAzkYpfcy3U7udglgctoV6x7tjaYqwHru6rVnwh4vgJU0KpvvLLahDtcUUIiItOGvD7hMMpxMOhl0Aatxtp41JOsnfnvKK_-YdC9sSY2_YJHDHs3exu1lkyGWCA_Lre1nBbky1kln5NfNFTRuw</recordid><startdate>20070701</startdate><enddate>20070701</enddate><creator>Nieminen, Tuomo</creator><creator>Matinheikki, Jussi</creator><creator>Nenonen, Arja</creator><creator>Kukkonen-Harjula, Katriina</creator><creator>Lindi, Virpi</creator><creator>Hämelahti, Päivi</creator><creator>Laaksonen, Reijo</creator><creator>Fan, Yue-Mei</creator><creator>Kähönen, Mika</creator><creator>Fogelholm, Mikael</creator><creator>Lehtimäki, Terho</creator><general>Elsevier Inc</general><general>Elsevier</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>7TS</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20070701</creationdate><title>The relationship of sterol regulatory element–binding protein cleavage–activation protein and apolipoprotein E gene polymorphisms with metabolic changes during weight reduction</title><author>Nieminen, Tuomo ; Matinheikki, Jussi ; Nenonen, Arja ; Kukkonen-Harjula, Katriina ; Lindi, Virpi ; Hämelahti, Päivi ; Laaksonen, Reijo ; Fan, Yue-Mei ; Kähönen, Mika ; Fogelholm, Mikael ; Lehtimäki, Terho</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-fc61105611b27ca1f5b73b6e98700e8be705b429562820b9f9845ec1175994893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Apolipoproteins E - genetics</topic><topic>Biological and medical sciences</topic><topic>Caloric Restriction</topic><topic>Cholesterol - blood</topic><topic>Cholesterol, LDL - blood</topic><topic>Endocrinology & Metabolism</topic><topic>Female</topic><topic>Humans</topic><topic>Intracellular Signaling Peptides and Proteins - genetics</topic><topic>Medical sciences</topic><topic>Membrane Proteins - genetics</topic><topic>Metabolic diseases</topic><topic>Middle Aged</topic><topic>Polymorphism, Genetic</topic><topic>Weight Loss - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nieminen, Tuomo</creatorcontrib><creatorcontrib>Matinheikki, Jussi</creatorcontrib><creatorcontrib>Nenonen, Arja</creatorcontrib><creatorcontrib>Kukkonen-Harjula, Katriina</creatorcontrib><creatorcontrib>Lindi, Virpi</creatorcontrib><creatorcontrib>Hämelahti, Päivi</creatorcontrib><creatorcontrib>Laaksonen, Reijo</creatorcontrib><creatorcontrib>Fan, Yue-Mei</creatorcontrib><creatorcontrib>Kähönen, Mika</creatorcontrib><creatorcontrib>Fogelholm, Mikael</creatorcontrib><creatorcontrib>Lehtimäki, Terho</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>Physical Education Index</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Metabolism, clinical and experimental</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nieminen, Tuomo</au><au>Matinheikki, Jussi</au><au>Nenonen, Arja</au><au>Kukkonen-Harjula, Katriina</au><au>Lindi, Virpi</au><au>Hämelahti, Päivi</au><au>Laaksonen, Reijo</au><au>Fan, Yue-Mei</au><au>Kähönen, Mika</au><au>Fogelholm, Mikael</au><au>Lehtimäki, Terho</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The relationship of sterol regulatory element–binding protein cleavage–activation protein and apolipoprotein E gene polymorphisms with metabolic changes during weight reduction</atitle><jtitle>Metabolism, clinical and experimental</jtitle><addtitle>Metabolism</addtitle><date>2007-07-01</date><risdate>2007</risdate><volume>56</volume><issue>7</issue><spage>876</spage><epage>880</epage><pages>876-880</pages><issn>0026-0495</issn><eissn>1532-8600</eissn><abstract>Abstract Sterol regulatory element–binding protein cleavage–activating protein (SCAP) and apolipoprotein E (apo E) regulate cellular and plasma lipid metabolism. Therefore, variations in the corresponding genes might influence weight reduction and obesity-associated metabolic changes. We investigated the relationships of SCAP (Ile796Val) and apo E polymorphisms on metabolic changes during weight reduction by using a 12-week very low-energy diet. Body composition, serum lipids, plasma glucose, and insulin were assessed in 78 healthy premenopausal women (initial body mass index, 34 ± 4 kg/m2 ; age, 40 ± 4 years) before and after the intervention. The SCAP genotype groups did not differ in the responses of any parameters measured during weight reduction. Apo E did not differentiate the weight loss, but the changes in total and low-density lipoprotein cholesterol for the genotype groups apo E ε 2/3, ε 3/3, as well as ε 3/4 and ε 4/4 combined were −0.94 ± 0.56 and −0.59 ± 0.32, −0.71 ± 0.49 and −0.49 ± 0.45, and −0.55 ± 0.47 and −0.37 ± 0.39 mmol/L, respectively ( P < .05 for both). In conclusion, neither the SCAP Ile796Val nor the apo E polymorphism was associated with weight loss in obese premenopausal women. However, the apo E—but not SCAP genotype—seems to be one of the modifying factors for serum cholesterol concentrations during very low-energy diet in obese premenopausal women.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>17570245</pmid><doi>10.1016/j.metabol.2007.02.003</doi><tpages>5</tpages></addata></record> |
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subjects | Adult Apolipoproteins E - genetics Biological and medical sciences Caloric Restriction Cholesterol - blood Cholesterol, LDL - blood Endocrinology & Metabolism Female Humans Intracellular Signaling Peptides and Proteins - genetics Medical sciences Membrane Proteins - genetics Metabolic diseases Middle Aged Polymorphism, Genetic Weight Loss - physiology |
title | The relationship of sterol regulatory element–binding protein cleavage–activation protein and apolipoprotein E gene polymorphisms with metabolic changes during weight reduction |
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