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Fasting plasma chenodeoxycholic acid and cholic acid concentrations are inversely correlated with insulin sensitivity in adults
Accumulating data suggest a novel role for bile acids (BAs) in modulating metabolic homeostasis. BA treatment has been shown to improve glucose tolerance and to increase energy expenditure in mice. Here, we investigated the relationship between fasting plasma BAs concentrations and metabolic paramet...
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Published in: | Nutrition & metabolism 2011-07, Vol.8 (1), p.48-48 |
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description | Accumulating data suggest a novel role for bile acids (BAs) in modulating metabolic homeostasis. BA treatment has been shown to improve glucose tolerance and to increase energy expenditure in mice. Here, we investigated the relationship between fasting plasma BAs concentrations and metabolic parameters in humans.
Fasting plasma glucose, insulin and lipid profile were measured in 14 healthy volunteers, 20 patients with type 2 diabetes (T2D), and 22 non-diabetic abdominally obese subjects. Insulin sensitivity was also assessed by the determination of the glucose infusion rate (GIR) during a hyperinsulinemic-euglycemic clamp in a subgroup of patients (9 healthy and 16 T2D subjects). Energy expenditure was measured by indirect calorimetry. Plasma cholic acid (CA), chenodeoxycholic acid (CDCA) and deoxycholic acid (DCA) concentrations were analyzed by gas chromatograph-mass spectrometry. In univariable analysis, a positive association was found between HOMA-IR and plasma CDCA (β = 0.09, p = 0.001), CA (β = 0.03, p = 0.09) and DCA concentrations (β = 0.07, p < 0.0001). Spearman analysis retrieved an inverse relationship between plasma CDCA (r = -0.44, p = 0.03), CA (r = -0.65, p = 0.001) and the GIR. HOMA-IR remained positively associated with CDCA (β = 0.11, p = 0.01), CA (β = 0.04, p = 0.01) and DCA (β = 0.06, p = 0.007) in multivariable analysis, after adjustment for age, gender, BMI, HbA1C and plasma lipid parameters. In contrast, HbA1c, energy expenditure and plasma lipid concentrations were not correlated with plasma BAs levels in multivariable analysis.
Both plasma CDCA, CA and DCA concentrations were negatively associated with insulin sensitivity in a wide range of subjects. |
doi_str_mv | 10.1186/1743-7075-8-48 |
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Fasting plasma glucose, insulin and lipid profile were measured in 14 healthy volunteers, 20 patients with type 2 diabetes (T2D), and 22 non-diabetic abdominally obese subjects. Insulin sensitivity was also assessed by the determination of the glucose infusion rate (GIR) during a hyperinsulinemic-euglycemic clamp in a subgroup of patients (9 healthy and 16 T2D subjects). Energy expenditure was measured by indirect calorimetry. Plasma cholic acid (CA), chenodeoxycholic acid (CDCA) and deoxycholic acid (DCA) concentrations were analyzed by gas chromatograph-mass spectrometry. In univariable analysis, a positive association was found between HOMA-IR and plasma CDCA (β = 0.09, p = 0.001), CA (β = 0.03, p = 0.09) and DCA concentrations (β = 0.07, p < 0.0001). Spearman analysis retrieved an inverse relationship between plasma CDCA (r = -0.44, p = 0.03), CA (r = -0.65, p = 0.001) and the GIR. HOMA-IR remained positively associated with CDCA (β = 0.11, p = 0.01), CA (β = 0.04, p = 0.01) and DCA (β = 0.06, p = 0.007) in multivariable analysis, after adjustment for age, gender, BMI, HbA1C and plasma lipid parameters. In contrast, HbA1c, energy expenditure and plasma lipid concentrations were not correlated with plasma BAs levels in multivariable analysis.
Both plasma CDCA, CA and DCA concentrations were negatively associated with insulin sensitivity in a wide range of subjects.</description><identifier>ISSN: 1743-7075</identifier><identifier>EISSN: 1743-7075</identifier><identifier>DOI: 10.1186/1743-7075-8-48</identifier><identifier>PMID: 21736725</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Bile acids ; Blood sugar ; Brief Communication ; Chenodeoxycholic acid ; Cholic acid ; energy expenditure ; Food and Nutrition ; FXR ; Human health and pathology ; hyperinsulinemic-euglycemic clamp ; insulin resistance ; Life Sciences ; Physiological aspects ; TGR5 ; Tissues and Organs ; type 2 diabetes</subject><ispartof>Nutrition & metabolism, 2011-07, Vol.8 (1), p.48-48</ispartof><rights>COPYRIGHT 2011 BioMed Central Ltd.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright ©2011 Cariou et al; licensee BioMed Central Ltd. 2011 Cariou et al; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b651t-3ed9f222add670fdca8fcd7285eb5e8fe84f3e94220d62c5e7ccb04595e547973</citedby><cites>FETCH-LOGICAL-b651t-3ed9f222add670fdca8fcd7285eb5e8fe84f3e94220d62c5e7ccb04595e547973</cites><orcidid>0000-0002-6252-9853 ; 0000-0002-4045-0503 ; 0000-0002-1580-8040</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/PMC3143920/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3143920/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,37013,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21736725$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://inserm.hal.science/inserm-00611430$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Cariou, Bertrand</creatorcontrib><creatorcontrib>Chetiveaux, Maud</creatorcontrib><creatorcontrib>Zaïr, Yassine</creatorcontrib><creatorcontrib>Pouteau, Etienne</creatorcontrib><creatorcontrib>Disse, Emmanuel</creatorcontrib><creatorcontrib>Guyomarc'h-Delasalle, Béatrice</creatorcontrib><creatorcontrib>Laville, Martine</creatorcontrib><creatorcontrib>Krempf, Michel</creatorcontrib><title>Fasting plasma chenodeoxycholic acid and cholic acid concentrations are inversely correlated with insulin sensitivity in adults</title><title>Nutrition & metabolism</title><addtitle>Nutr Metab (Lond)</addtitle><description>Accumulating data suggest a novel role for bile acids (BAs) in modulating metabolic homeostasis. BA treatment has been shown to improve glucose tolerance and to increase energy expenditure in mice. Here, we investigated the relationship between fasting plasma BAs concentrations and metabolic parameters in humans.
Fasting plasma glucose, insulin and lipid profile were measured in 14 healthy volunteers, 20 patients with type 2 diabetes (T2D), and 22 non-diabetic abdominally obese subjects. Insulin sensitivity was also assessed by the determination of the glucose infusion rate (GIR) during a hyperinsulinemic-euglycemic clamp in a subgroup of patients (9 healthy and 16 T2D subjects). Energy expenditure was measured by indirect calorimetry. Plasma cholic acid (CA), chenodeoxycholic acid (CDCA) and deoxycholic acid (DCA) concentrations were analyzed by gas chromatograph-mass spectrometry. In univariable analysis, a positive association was found between HOMA-IR and plasma CDCA (β = 0.09, p = 0.001), CA (β = 0.03, p = 0.09) and DCA concentrations (β = 0.07, p < 0.0001). Spearman analysis retrieved an inverse relationship between plasma CDCA (r = -0.44, p = 0.03), CA (r = -0.65, p = 0.001) and the GIR. HOMA-IR remained positively associated with CDCA (β = 0.11, p = 0.01), CA (β = 0.04, p = 0.01) and DCA (β = 0.06, p = 0.007) in multivariable analysis, after adjustment for age, gender, BMI, HbA1C and plasma lipid parameters. In contrast, HbA1c, energy expenditure and plasma lipid concentrations were not correlated with plasma BAs levels in multivariable analysis.
Both plasma CDCA, CA and DCA concentrations were negatively associated with insulin sensitivity in a wide range of subjects.</description><subject>Bile acids</subject><subject>Blood sugar</subject><subject>Brief Communication</subject><subject>Chenodeoxycholic acid</subject><subject>Cholic acid</subject><subject>energy expenditure</subject><subject>Food and Nutrition</subject><subject>FXR</subject><subject>Human health and pathology</subject><subject>hyperinsulinemic-euglycemic clamp</subject><subject>insulin resistance</subject><subject>Life Sciences</subject><subject>Physiological aspects</subject><subject>TGR5</subject><subject>Tissues and Organs</subject><subject>type 2 diabetes</subject><issn>1743-7075</issn><issn>1743-7075</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp1kstvEzEQh1cIREvhyhGtxAEhscXP9e6lUlRRGikSEo-z5diziatdu9je0Jz413HYEiVQ5IPtmW9-9jyK4iVG5xg39XssGK0EErxqKtY8Kk73hscH55PiWYw3CFHKWvS0OCFY0FoQflr8vFIxWbcqb3sVB1XqNThvwN9t9dr3VpdKW1MqZ8rDu_ZOg0tBJetdLFWA0roNhAj9NjtDgF4lMOUPm9bZE8feujKCizbZjU3bbCuVGfsUnxdPOtVHeHG_nxXfrj58vbyuFp8-zi9ni2pZc5wqCqbtCCHKmFqgzmjVdNoI0nBYcmg6aFhHoWWEIFMTzUFovUSMtxw4E62gZ8V80jVe3cjbYAcVttIrK38bfFhJFZLVPUjC8uKY6QZpBpq2mC0xrTuOUc0F51nrYtK6HZcDmKkS_ZHoscfZtVz5jaSY0ZagLPBuElj_FXY9W8hcLgiDRKjGGUcbnPHZhC-t_897xx7tB7nrvdz1XjaSNVnjzf2fg_8-QkxysFFD3ysHfoyyEW0takJ25OuJXKlcDOs6nzX1jpYzUufCYIbqTJ0_QOVlYLB5PKCz2X4U8PYoIDMJ7tJKjTHK-ZfPD4rr4GMM0O1zxUjuxv7f7F4ddmSP_5lz-gvNEf4s</recordid><startdate>20110707</startdate><enddate>20110707</enddate><creator>Cariou, Bertrand</creator><creator>Chetiveaux, Maud</creator><creator>Zaïr, Yassine</creator><creator>Pouteau, Etienne</creator><creator>Disse, Emmanuel</creator><creator>Guyomarc'h-Delasalle, Béatrice</creator><creator>Laville, Martine</creator><creator>Krempf, Michel</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-6252-9853</orcidid><orcidid>https://orcid.org/0000-0002-4045-0503</orcidid><orcidid>https://orcid.org/0000-0002-1580-8040</orcidid></search><sort><creationdate>20110707</creationdate><title>Fasting plasma chenodeoxycholic acid and cholic acid concentrations are inversely correlated with insulin sensitivity in adults</title><author>Cariou, Bertrand ; 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BA treatment has been shown to improve glucose tolerance and to increase energy expenditure in mice. Here, we investigated the relationship between fasting plasma BAs concentrations and metabolic parameters in humans.
Fasting plasma glucose, insulin and lipid profile were measured in 14 healthy volunteers, 20 patients with type 2 diabetes (T2D), and 22 non-diabetic abdominally obese subjects. Insulin sensitivity was also assessed by the determination of the glucose infusion rate (GIR) during a hyperinsulinemic-euglycemic clamp in a subgroup of patients (9 healthy and 16 T2D subjects). Energy expenditure was measured by indirect calorimetry. Plasma cholic acid (CA), chenodeoxycholic acid (CDCA) and deoxycholic acid (DCA) concentrations were analyzed by gas chromatograph-mass spectrometry. In univariable analysis, a positive association was found between HOMA-IR and plasma CDCA (β = 0.09, p = 0.001), CA (β = 0.03, p = 0.09) and DCA concentrations (β = 0.07, p < 0.0001). Spearman analysis retrieved an inverse relationship between plasma CDCA (r = -0.44, p = 0.03), CA (r = -0.65, p = 0.001) and the GIR. HOMA-IR remained positively associated with CDCA (β = 0.11, p = 0.01), CA (β = 0.04, p = 0.01) and DCA (β = 0.06, p = 0.007) in multivariable analysis, after adjustment for age, gender, BMI, HbA1C and plasma lipid parameters. In contrast, HbA1c, energy expenditure and plasma lipid concentrations were not correlated with plasma BAs levels in multivariable analysis.
Both plasma CDCA, CA and DCA concentrations were negatively associated with insulin sensitivity in a wide range of subjects.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>21736725</pmid><doi>10.1186/1743-7075-8-48</doi><orcidid>https://orcid.org/0000-0002-6252-9853</orcidid><orcidid>https://orcid.org/0000-0002-4045-0503</orcidid><orcidid>https://orcid.org/0000-0002-1580-8040</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bile acids Blood sugar Brief Communication Chenodeoxycholic acid Cholic acid energy expenditure Food and Nutrition FXR Human health and pathology hyperinsulinemic-euglycemic clamp insulin resistance Life Sciences Physiological aspects TGR5 Tissues and Organs type 2 diabetes |
title | Fasting plasma chenodeoxycholic acid and cholic acid concentrations are inversely correlated with insulin sensitivity in adults |
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