Plasma Lipidomic Profile Signature of Hypertension in Mexican American Families: Specific Role of Diacylglycerols
Both as a component of metabolic syndrome and as an independent entity, hypertension poses a continued challenge with regard to its diagnosis, pathogenesis, and treatment. Previous studies have documented connections between hypertension and indicators of lipid metabolism. Novel technologies, such a...
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Published in: | Hypertension (Dallas, Tex. 1979) Vol. 62; no. 3; pp. 621 - 626 |
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Main Authors: | , , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
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Hagerstown, MD
American Heart Association, Inc
01-09-2013
Lippincott Williams & Wilkins |
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Abstract | Both as a component of metabolic syndrome and as an independent entity, hypertension poses a continued challenge with regard to its diagnosis, pathogenesis, and treatment. Previous studies have documented connections between hypertension and indicators of lipid metabolism. Novel technologies, such as plasma lipidomic profiling, promise a better understanding of disorders in which there is a derangement of the lipid metabolism. However, association of plasma lipidomic profiles with hypertension in a high-risk population, such as Mexican Americans, has not been evaluated before. Using the rich data and sample resource from the ongoing San Antonio Family Heart Study, we conducted plasma lipidomic profiling by combining high-performance liquid chromatography with tandem mass spectroscopy to characterize 319 lipid species in 1192 individuals from 42 large and extended Mexican American families. Robust statistical analyses using polygenic regression models, liability threshold models, and bivariate trait analyses implemented in the SOLAR software were conducted after accounting for obesity, insulin resistance, and relative abundance of various lipoprotein fractions. Diacylglycerols, in general, and the DG 16:0/22:5 and DG 16:0/22:6 lipid species, in particular, were significantly associated with systolic blood pressure (SBP), diastolic blood pressure (DBP), and mean arterial pressure (MAP), as well as liability of incident hypertension measured during 7140.17 person-years of follow-up. Four lipid species, including the DG 16:0/22:5 and DG 16:0/22:6 species, showed significant genetic correlations with the liability of hypertension in bivariate trait analyses. Our results demonstrate the value of plasma lipidomic profiling in the context of hypertension and identify disturbance of diacylglycerol metabolism as an independent biomarker of hypertension. |
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AbstractList | Both as a component of metabolic syndrome and as an independent entity, hypertension poses a continued challenge with regard to its diagnosis, pathogenesis, and treatment. Previous studies have documented connections between hypertension and indicators of lipid metabolism. Novel technologies, such as plasma lipidomic profiling, promise a better understanding of disorders in which there is a derangement of the lipid metabolism. However, association of plasma lipidomic profiles with hypertension in a high-risk population, such as Mexican Americans, has not been evaluated before. Using the rich data and sample resource from the ongoing San Antonio Family Heart Study, we conducted plasma lipidomic profiling by combining high-performance liquid chromatography with tandem mass spectroscopy to characterize 319 lipid species in 1192 individuals from 42 large and extended Mexican American families. Robust statistical analyses using polygenic regression models, liability threshold models, and bivariate trait analyses implemented in the SOLAR software were conducted after accounting for obesity, insulin resistance, and relative abundance of various lipoprotein fractions. Diacylglycerols, in general, and the DG 16:0/22:5 and DG 16:0/22:6 lipid species, in particular, were significantly associated with systolic blood pressure (SBP), diastolic blood pressure (DBP), and mean arterial pressure (MAP), as well as liability of incident hypertension measured during 7140.17 person-years of follow-up. Four lipid species, including the DG 16:0/22:5 and DG 16:0/22:6 species, showed significant genetic correlations with the liability of hypertension in bivariate trait analyses. Our results demonstrate the value of plasma lipidomic profiling in the context of hypertension and identify disturbance of diacylglycerol metabolism as an independent biomarker of hypertension. Both as a component of metabolic syndrome and as an independent entity, hypertension poses a continued challenge with regard to its diagnosis, pathogenesis and treatment. Previous studies have documented connections between hypertension and indicators of lipid metabolism. Novel technologies like plasma lipidomic profiling promise a better understanding of disorders in which there is a derangement of the lipid metabolism. However, association of plasma lipidomic profiles with hypertension in a high-risk population, like Mexican Americans, has not been evaluated before. Using the rich data and sample resource from the ongoing San Antonio Family Heart Study, we conducted plasma lipidomic profiling by combining high performance liquid chromatography with tandem mass spectroscopy to characterize 319 lipid species in 1192 individuals from 42 large and extended Mexican American families. Robust statistical analyses employing polygenic regression models, liability threshold models and bivariate trait analyses implemented in the SOLAR software were conducted after accounting for obesity, insulin resistance and relative abundance of various lipoprotein fractions. Diacylglycerols in general and the DG 16:0/22:5 and DG 16:0/22:6 lipid species in particular were significantly associated with systolic, diastolic and mean arterial pressures as well as liability of incident hypertension measured during 7767.42 person-years of follow-up. Four lipid species, including the DG 16:0/22:5 and DG 16:0/22:6 species, showed significant genetic correlations with the liability of hypertension in bivariate trait analyses. Our results demonstrate the value of plasma lipidomic profiling in the context of hypertension and identify disturbance of diacyglycerol metabolism as an independent biomarker of hypertension. |
Author | Jowett, Jeremy B. Mahaney, Michael C. Weir, Jacquelyn M. Dyer, Thomas D. Curran, Joanne E. Johnson, Matthew P. Meikle, Peter J. Rainwater, David L. Almasy, Laura Comuzzie, Anthony G. Kulkarni, Hemant Blangero, John Bellis, Claire Mamtani, Manju Barlow, Christopher K. |
AuthorAffiliation | From the Department of Genetics, Texas Biomedical Research Institute, San Antonio, TX (H.K., M.M., C.B., T.D.D., M.P.J., D.L.R., L.A., M.C.M., A.G.C., J.B., J.E.C.); and Baker IDI Heart and Diabetes Institute, Melbourne, Victoria, Australia (P.J.M., J.M.W., C.K.B., J.B.J.) |
AuthorAffiliation_xml | – name: From the Department of Genetics, Texas Biomedical Research Institute, San Antonio, TX (H.K., M.M., C.B., T.D.D., M.P.J., D.L.R., L.A., M.C.M., A.G.C., J.B., J.E.C.); and Baker IDI Heart and Diabetes Institute, Melbourne, Victoria, Australia (P.J.M., J.M.W., C.K.B., J.B.J.) – name: 2 Baker IDI Heart and Diabetes Institute, Melbourne VIC, 3004, Australia – name: 1 Department of Genetics, Texas Biomedical Research Institute, San Antonio TX, 78227 USA |
Author_xml | – sequence: 1 givenname: Hemant surname: Kulkarni fullname: Kulkarni, Hemant organization: From the Department of Genetics, Texas Biomedical Research Institute, San Antonio, TX (H.K., M.M., C.B., T.D.D., M.P.J., D.L.R., L.A., M.C.M., A.G.C., J.B., J.E.C.); and Baker IDI Heart and Diabetes Institute, Melbourne, Victoria, Australia (P.J.M., J.M.W., C.K.B., J.B.J.) – sequence: 2 givenname: Peter surname: Meikle middlename: J. fullname: Meikle, Peter J. – sequence: 3 givenname: Manju surname: Mamtani fullname: Mamtani, Manju – sequence: 4 givenname: Jacquelyn surname: Weir middlename: M. fullname: Weir, Jacquelyn M. – sequence: 5 givenname: Christopher surname: Barlow middlename: K. fullname: Barlow, Christopher K. – sequence: 6 givenname: Jeremy surname: Jowett middlename: B. fullname: Jowett, Jeremy B. – sequence: 7 givenname: Claire surname: Bellis fullname: Bellis, Claire – sequence: 8 givenname: Thomas surname: Dyer middlename: D. fullname: Dyer, Thomas D. – sequence: 9 givenname: Matthew surname: Johnson middlename: P. fullname: Johnson, Matthew P. – sequence: 10 givenname: David surname: Rainwater middlename: L. fullname: Rainwater, David L. – sequence: 11 givenname: Laura surname: Almasy fullname: Almasy, Laura – sequence: 12 givenname: Michael surname: Mahaney middlename: C. fullname: Mahaney, Michael C. – sequence: 13 givenname: Anthony surname: Comuzzie middlename: G. fullname: Comuzzie, Anthony G. – sequence: 14 givenname: John surname: Blangero fullname: Blangero, John – sequence: 15 givenname: Joanne surname: Curran middlename: E. fullname: Curran, Joanne E. |
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Keywords | Human Hypertension Biological fluid Mexican Americans Family study Diacylglycerol Lipids Cardiovascular disease Latinamerican Profile Blood plasma lipid species Family environment Arterial pressure Blood pressure Hemodynamics Circulatory system Cardiology Species lipidomics blood pressure hypertension |
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SubjectTerms | Adult Aged Arterial hypertension. Arterial hypotension Biological and medical sciences Blood and lymphatic vessels Cardiology. Vascular system Chromatography, High Pressure Liquid Cross-Sectional Studies Diglycerides - blood Female Humans Hypertension - blood Hypertension - ethnology Insulin Resistance - ethnology Insulin Resistance - physiology Lipid Metabolism - physiology Lipids - blood Male Medical sciences Mexican Americans Middle Aged Tandem Mass Spectrometry |
Title | Plasma Lipidomic Profile Signature of Hypertension in Mexican American Families: Specific Role of Diacylglycerols |
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