Glucose Tolerance and Free Fatty Acid Metabolism in Adults with Variations in TCF7L2 rs7903146
Abstract Objective TCF7L2 variant rs7903146 is associated with increased risk for Type 2 diabetes. We investigated the effect of TCF7L2 variant rs7903146 and glucose tolerance on free fatty acid (FFA) metabolism. Research design and methods We recruited 120 individuals, half homozygous for the major...
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description | Abstract Objective TCF7L2 variant rs7903146 is associated with increased risk for Type 2 diabetes. We investigated the effect of TCF7L2 variant rs7903146 and glucose tolerance on free fatty acid (FFA) metabolism. Research design and methods We recruited 120 individuals, half homozygous for the major CC allele and half homozygous for the minor TT allele at rs7903146; each underwent a 2-h, 75 g oral glucose tolerance test (OGTT). Plasma glucose, insulin and free fatty acid concentrations were measured on blood collected before and during the OGTT. Results Total FFA concentrations and percent FA species during OGTT were not different in CC and TT carriers when males and females were considered together. However, monounsaturated fatty acid (MUFA) concentrations and percentages were greater in TT than CC females during the OGTT. TT carriers with high HOMA-IR had significantly greater fasting FFA concentrations, lower disposition index (DI) and greater AUC of glucose than high HOMA-IR CC carriers, whereas no such differences were observed in the low HOMA-IR group. We found that fasting (826 ± 25 vs. 634 ± 22 μmol/L, P < 0.0001) and OGTT plasma FFA concentrations were greater in IGT than NGT subjects, and the difference remained after adjusting for sex, age, BMI, and genotype. Finally, IGT subjects had greater MUFA concentrations and percentages than NGT subjects during OGTT. Conclusions Despite similar fasting insulin and glucose, fasting plasma FFA are greater in IGT than NGT adults. Insulin resistance and sex influence plasma FFA responses amongst carriers of the minor T allele of TCF7L2 rs7903146. |
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We investigated the effect of TCF7L2 variant rs7903146 and glucose tolerance on free fatty acid (FFA) metabolism. Research design and methods We recruited 120 individuals, half homozygous for the major CC allele and half homozygous for the minor TT allele at rs7903146; each underwent a 2-h, 75 g oral glucose tolerance test (OGTT). Plasma glucose, insulin and free fatty acid concentrations were measured on blood collected before and during the OGTT. Results Total FFA concentrations and percent FA species during OGTT were not different in CC and TT carriers when males and females were considered together. However, monounsaturated fatty acid (MUFA) concentrations and percentages were greater in TT than CC females during the OGTT. TT carriers with high HOMA-IR had significantly greater fasting FFA concentrations, lower disposition index (DI) and greater AUC of glucose than high HOMA-IR CC carriers, whereas no such differences were observed in the low HOMA-IR group. We found that fasting (826 ± 25 vs. 634 ± 22 μmol/L, P < 0.0001) and OGTT plasma FFA concentrations were greater in IGT than NGT subjects, and the difference remained after adjusting for sex, age, BMI, and genotype. Finally, IGT subjects had greater MUFA concentrations and percentages than NGT subjects during OGTT. Conclusions Despite similar fasting insulin and glucose, fasting plasma FFA are greater in IGT than NGT adults. Insulin resistance and sex influence plasma FFA responses amongst carriers of the minor T allele of TCF7L2 rs7903146.</description><identifier>ISSN: 0026-0495</identifier><identifier>EISSN: 1532-8600</identifier><identifier>DOI: 10.1016/j.metabol.2016.11.018</identifier><identifier>PMID: 28183453</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Aged ; Endocrinology & Metabolism ; Fatty acids ; Fatty Acids, Nonesterified - metabolism ; Female ; Free fatty acids ; Genetic Variation - genetics ; Genotype ; Glucose Tolerance Test ; Heterozygote ; Humans ; Insulin - blood ; Insulin action ; Insulin secretion ; Male ; Middle Aged ; Polymorphism, Single Nucleotide ; Prediabetes ; Transcription Factor 7-Like 2 Protein - genetics ; Transcription Factor 7-Like 2 Protein - metabolism ; Young Adult</subject><ispartof>Metabolism, clinical and experimental, 2017-03, Vol.68, p.55-63</ispartof><rights>2016 Elsevier Inc.</rights><rights>Copyright © 2016 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c522t-e5e91efba667deb97e641dc817b1005cd55a192bb0568e0ab283a7c7e81df4c03</citedby><cites>FETCH-LOGICAL-c522t-e5e91efba667deb97e641dc817b1005cd55a192bb0568e0ab283a7c7e81df4c03</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.2016.11.018$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28183453$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lu, Jin</creatorcontrib><creatorcontrib>Varghese, Ron T</creatorcontrib><creatorcontrib>Zhou, Lianzhen</creatorcontrib><creatorcontrib>Vella, Adrian</creatorcontrib><creatorcontrib>Jensen, Michael D</creatorcontrib><title>Glucose Tolerance and Free Fatty Acid Metabolism in Adults with Variations in TCF7L2 rs7903146</title><title>Metabolism, clinical and experimental</title><addtitle>Metabolism</addtitle><description>Abstract Objective TCF7L2 variant rs7903146 is associated with increased risk for Type 2 diabetes. We investigated the effect of TCF7L2 variant rs7903146 and glucose tolerance on free fatty acid (FFA) metabolism. Research design and methods We recruited 120 individuals, half homozygous for the major CC allele and half homozygous for the minor TT allele at rs7903146; each underwent a 2-h, 75 g oral glucose tolerance test (OGTT). Plasma glucose, insulin and free fatty acid concentrations were measured on blood collected before and during the OGTT. Results Total FFA concentrations and percent FA species during OGTT were not different in CC and TT carriers when males and females were considered together. However, monounsaturated fatty acid (MUFA) concentrations and percentages were greater in TT than CC females during the OGTT. TT carriers with high HOMA-IR had significantly greater fasting FFA concentrations, lower disposition index (DI) and greater AUC of glucose than high HOMA-IR CC carriers, whereas no such differences were observed in the low HOMA-IR group. We found that fasting (826 ± 25 vs. 634 ± 22 μmol/L, P < 0.0001) and OGTT plasma FFA concentrations were greater in IGT than NGT subjects, and the difference remained after adjusting for sex, age, BMI, and genotype. Finally, IGT subjects had greater MUFA concentrations and percentages than NGT subjects during OGTT. Conclusions Despite similar fasting insulin and glucose, fasting plasma FFA are greater in IGT than NGT adults. Insulin resistance and sex influence plasma FFA responses amongst carriers of the minor T allele of TCF7L2 rs7903146.</description><subject>Adult</subject><subject>Aged</subject><subject>Endocrinology & Metabolism</subject><subject>Fatty acids</subject><subject>Fatty Acids, Nonesterified - metabolism</subject><subject>Female</subject><subject>Free fatty acids</subject><subject>Genetic Variation - genetics</subject><subject>Genotype</subject><subject>Glucose Tolerance Test</subject><subject>Heterozygote</subject><subject>Humans</subject><subject>Insulin - blood</subject><subject>Insulin action</subject><subject>Insulin secretion</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Prediabetes</subject><subject>Transcription Factor 7-Like 2 Protein - genetics</subject><subject>Transcription Factor 7-Like 2 Protein - metabolism</subject><subject>Young Adult</subject><issn>0026-0495</issn><issn>1532-8600</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkkGP0zAQhSMEYsvCTwD5yCVhJokd57KoqrYLUhEHCkcsx5myLm682Mmi_nsctayACyfLmvfe2PNNlr1EKBBQvNkXBxp1511RpmuBWADKR9kCeVXmUgA8zhYApcihbvlF9izGPQA0jRRPs4tSoqxqXi2yrzduMj4S23pHQQ-GmB56tg5EbK3H8ciWxvbsw6mXjQdmB7bsJzdG9tOOt-yLDlaP1g9xrmxX62ZTshCbFiqsxfPsyU67SC_O52X2eX29Xb3LNx9v3q-Wm9zwshxz4tQi7TotRNNT1zYkauyNxKZDAG56zjW2ZdcBF5JAd6WsdGMaktjvagPVZXZ1yr2bugP1hoYxaKfugj3ocFReW_V3ZbC36pu_V7wCyQWmgNfngOB_TBRHdbDRkHN6ID9FhVI0vK7SqJOUn6Qm-BgD7R7aIKiZjdqrMxs1s1GIKrFJvld_vvHB9RtGErw9CShN6t5SUNFYSkh6G8iMqvf2vy2u_kkwzg7WaPedjhT3fgpDwqBQxVKB-jQvyLwf6VfJDm31Cwy1txo</recordid><startdate>20170301</startdate><enddate>20170301</enddate><creator>Lu, Jin</creator><creator>Varghese, Ron T</creator><creator>Zhou, Lianzhen</creator><creator>Vella, Adrian</creator><creator>Jensen, Michael D</creator><general>Elsevier Inc</general><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></search><sort><creationdate>20170301</creationdate><title>Glucose Tolerance and Free Fatty Acid Metabolism in Adults with Variations in TCF7L2 rs7903146</title><author>Lu, Jin ; Varghese, Ron T ; Zhou, Lianzhen ; Vella, Adrian ; Jensen, Michael D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c522t-e5e91efba667deb97e641dc817b1005cd55a192bb0568e0ab283a7c7e81df4c03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Endocrinology & Metabolism</topic><topic>Fatty acids</topic><topic>Fatty Acids, Nonesterified - metabolism</topic><topic>Female</topic><topic>Free fatty acids</topic><topic>Genetic Variation - genetics</topic><topic>Genotype</topic><topic>Glucose Tolerance Test</topic><topic>Heterozygote</topic><topic>Humans</topic><topic>Insulin - blood</topic><topic>Insulin action</topic><topic>Insulin secretion</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Prediabetes</topic><topic>Transcription Factor 7-Like 2 Protein - genetics</topic><topic>Transcription Factor 7-Like 2 Protein - metabolism</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lu, Jin</creatorcontrib><creatorcontrib>Varghese, Ron T</creatorcontrib><creatorcontrib>Zhou, Lianzhen</creatorcontrib><creatorcontrib>Vella, Adrian</creatorcontrib><creatorcontrib>Jensen, Michael D</creatorcontrib><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><jtitle>Metabolism, clinical and experimental</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lu, Jin</au><au>Varghese, Ron T</au><au>Zhou, Lianzhen</au><au>Vella, Adrian</au><au>Jensen, Michael D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Glucose Tolerance and Free Fatty Acid Metabolism in Adults with Variations in TCF7L2 rs7903146</atitle><jtitle>Metabolism, clinical and experimental</jtitle><addtitle>Metabolism</addtitle><date>2017-03-01</date><risdate>2017</risdate><volume>68</volume><spage>55</spage><epage>63</epage><pages>55-63</pages><issn>0026-0495</issn><eissn>1532-8600</eissn><abstract>Abstract Objective TCF7L2 variant rs7903146 is associated with increased risk for Type 2 diabetes. We investigated the effect of TCF7L2 variant rs7903146 and glucose tolerance on free fatty acid (FFA) metabolism. Research design and methods We recruited 120 individuals, half homozygous for the major CC allele and half homozygous for the minor TT allele at rs7903146; each underwent a 2-h, 75 g oral glucose tolerance test (OGTT). Plasma glucose, insulin and free fatty acid concentrations were measured on blood collected before and during the OGTT. Results Total FFA concentrations and percent FA species during OGTT were not different in CC and TT carriers when males and females were considered together. However, monounsaturated fatty acid (MUFA) concentrations and percentages were greater in TT than CC females during the OGTT. TT carriers with high HOMA-IR had significantly greater fasting FFA concentrations, lower disposition index (DI) and greater AUC of glucose than high HOMA-IR CC carriers, whereas no such differences were observed in the low HOMA-IR group. We found that fasting (826 ± 25 vs. 634 ± 22 μmol/L, P < 0.0001) and OGTT plasma FFA concentrations were greater in IGT than NGT subjects, and the difference remained after adjusting for sex, age, BMI, and genotype. Finally, IGT subjects had greater MUFA concentrations and percentages than NGT subjects during OGTT. Conclusions Despite similar fasting insulin and glucose, fasting plasma FFA are greater in IGT than NGT adults. Insulin resistance and sex influence plasma FFA responses amongst carriers of the minor T allele of TCF7L2 rs7903146.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28183453</pmid><doi>10.1016/j.metabol.2016.11.018</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Endocrinology & Metabolism Fatty acids Fatty Acids, Nonesterified - metabolism Female Free fatty acids Genetic Variation - genetics Genotype Glucose Tolerance Test Heterozygote Humans Insulin - blood Insulin action Insulin secretion Male Middle Aged Polymorphism, Single Nucleotide Prediabetes Transcription Factor 7-Like 2 Protein - genetics Transcription Factor 7-Like 2 Protein - metabolism Young Adult |
title | Glucose Tolerance and Free Fatty Acid Metabolism in Adults with Variations in TCF7L2 rs7903146 |
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