Plasma oxidizability in subjects with normal glucose tolerance, impaired glucose tolerance, and NIDDM
Plasma oxidizability in subjects with normal glucose tolerance, impaired glucose tolerance, and NIDDM. S M Haffner , A Agil , L Mykkanen , M P Stern and I Jialal Department of Medicine, University of Texas Health Science Center at San Antonio, Texas 78284-7873, USA. Abstract OBJECTIVE--Several lines...
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Published in | Diabetes care Vol. 18; no. 5; pp. 646 - 653 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Alexandria, VA
American Diabetes Association
01.05.1995
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Subjects | |
Online Access | Get full text |
ISSN | 0149-5992 1935-5548 |
DOI | 10.2337/diacare.18.5.646 |
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Abstract | Plasma oxidizability in subjects with normal glucose tolerance, impaired glucose tolerance, and NIDDM.
S M Haffner ,
A Agil ,
L Mykkanen ,
M P Stern and
I Jialal
Department of Medicine, University of Texas Health Science Center at San Antonio, Texas 78284-7873, USA.
Abstract
OBJECTIVE--Several lines of evidence support an atherogenic role for oxidized low-density lipoprotein (LDL). Studies on LDL
oxidation in diabetes to date have examined LDL isolated from plasma, but have failed to evaluate the other pro- and antioxidant
factors present in vivo, the balance of which could be crucial in determining the susceptibility of LDL to lipid peroxidation.
RESEARCH DESIGN AND METHODS--We examined the oxidizability of plasma from Mexican-Americans in the San Antonio Heart Study.
The oxidizability of plasma in 75 subjects with normal glucose tolerance (NGT), impaired glucose tolerance (IGT), and non-insulin-dependent
diabetes mellitus (NIDDM) was studied after co-incubation with a free radical initiator, 2,2'-azobis-2-amidinopropane hydrochloride
(AAPH). Lipid peroxide (LPO) levels were measured by a modified fluorimetric assay. RESULTS--Baseline LPO levels (mumol/l;
means +/- SE) were similar in the three glucose tolerance categories (NGT, 1.99 +/- 0.07; IGT, 1.88 +/- 0.07; NIDDM, 1.97
+/- 0.07; P = 0.521). However, after incubation with AAPH (NGT, 4.30 +/- 0.20; IGT, 4.45 +/- 0.20; NIDDM, 5.35 +/- 0.20; P
= 0.003), the diabetic plasma had significantly greater amounts of LPOs compared with the other two groups. There was no significant
difference in LPOs between the NGT and IGT groups. The statistical significance of increased oxidizability of the diabetic
plasma persisted after exclusion of patients who smoked cigarettes (n = 15) or who had vascular disease (n = 4). CONCLUSIONS--In
conclusion, this study shows that the plasma of Mexican-American subjects with NIDDM is more prone to lipid peroxidation than
that of non-Hispanic whites. |
---|---|
AbstractList | Plasma oxidizability in subjects with normal glucose tolerance, impaired glucose tolerance, and NIDDM.
S M Haffner ,
A Agil ,
L Mykkanen ,
M P Stern and
I Jialal
Department of Medicine, University of Texas Health Science Center at San Antonio, Texas 78284-7873, USA.
Abstract
OBJECTIVE--Several lines of evidence support an atherogenic role for oxidized low-density lipoprotein (LDL). Studies on LDL
oxidation in diabetes to date have examined LDL isolated from plasma, but have failed to evaluate the other pro- and antioxidant
factors present in vivo, the balance of which could be crucial in determining the susceptibility of LDL to lipid peroxidation.
RESEARCH DESIGN AND METHODS--We examined the oxidizability of plasma from Mexican-Americans in the San Antonio Heart Study.
The oxidizability of plasma in 75 subjects with normal glucose tolerance (NGT), impaired glucose tolerance (IGT), and non-insulin-dependent
diabetes mellitus (NIDDM) was studied after co-incubation with a free radical initiator, 2,2'-azobis-2-amidinopropane hydrochloride
(AAPH). Lipid peroxide (LPO) levels were measured by a modified fluorimetric assay. RESULTS--Baseline LPO levels (mumol/l;
means +/- SE) were similar in the three glucose tolerance categories (NGT, 1.99 +/- 0.07; IGT, 1.88 +/- 0.07; NIDDM, 1.97
+/- 0.07; P = 0.521). However, after incubation with AAPH (NGT, 4.30 +/- 0.20; IGT, 4.45 +/- 0.20; NIDDM, 5.35 +/- 0.20; P
= 0.003), the diabetic plasma had significantly greater amounts of LPOs compared with the other two groups. There was no significant
difference in LPOs between the NGT and IGT groups. The statistical significance of increased oxidizability of the diabetic
plasma persisted after exclusion of patients who smoked cigarettes (n = 15) or who had vascular disease (n = 4). CONCLUSIONS--In
conclusion, this study shows that the plasma of Mexican-American subjects with NIDDM is more prone to lipid peroxidation than
that of non-Hispanic whites. Several lines of evidence support an atherogenic role for oxidized low-density lipoprotein (LDL). Studies on LDL oxidation in diabetes to date have examined LDL isolated from plasma, but have failed to evaluate the other pro- and antioxidant factors present in vivo, the balance of which could be crucial in determining the susceptibility of LDL to lipid peroxidation.OBJECTIVESeveral lines of evidence support an atherogenic role for oxidized low-density lipoprotein (LDL). Studies on LDL oxidation in diabetes to date have examined LDL isolated from plasma, but have failed to evaluate the other pro- and antioxidant factors present in vivo, the balance of which could be crucial in determining the susceptibility of LDL to lipid peroxidation.We examined the oxidizability of plasma from Mexican-Americans in the San Antonio Heart Study. The oxidizability of plasma in 75 subjects with normal glucose tolerance (NGT), impaired glucose tolerance (IGT), and non-insulin-dependent diabetes mellitus (NIDDM) was studied after co-incubation with a free radical initiator, 2,2'-azobis-2-amidinopropane hydrochloride (AAPH). Lipid peroxide (LPO) levels were measured by a modified fluorimetric assay.RESEARCH DESIGN AND METHODSWe examined the oxidizability of plasma from Mexican-Americans in the San Antonio Heart Study. The oxidizability of plasma in 75 subjects with normal glucose tolerance (NGT), impaired glucose tolerance (IGT), and non-insulin-dependent diabetes mellitus (NIDDM) was studied after co-incubation with a free radical initiator, 2,2'-azobis-2-amidinopropane hydrochloride (AAPH). Lipid peroxide (LPO) levels were measured by a modified fluorimetric assay.Baseline LPO levels (mumol/l; means +/- SE) were similar in the three glucose tolerance categories (NGT, 1.99 +/- 0.07; IGT, 1.88 +/- 0.07; NIDDM, 1.97 +/- 0.07; P = 0.521). However, after incubation with AAPH (NGT, 4.30 +/- 0.20; IGT, 4.45 +/- 0.20; NIDDM, 5.35 +/- 0.20; P = 0.003), the diabetic plasma had significantly greater amounts of LPOs compared with the other two groups. There was no significant difference in LPOs between the NGT and IGT groups. The statistical significance of increased oxidizability of the diabetic plasma persisted after exclusion of patients who smoked cigarettes (n = 15) or who had vascular disease (n = 4).RESULTSBaseline LPO levels (mumol/l; means +/- SE) were similar in the three glucose tolerance categories (NGT, 1.99 +/- 0.07; IGT, 1.88 +/- 0.07; NIDDM, 1.97 +/- 0.07; P = 0.521). However, after incubation with AAPH (NGT, 4.30 +/- 0.20; IGT, 4.45 +/- 0.20; NIDDM, 5.35 +/- 0.20; P = 0.003), the diabetic plasma had significantly greater amounts of LPOs compared with the other two groups. There was no significant difference in LPOs between the NGT and IGT groups. The statistical significance of increased oxidizability of the diabetic plasma persisted after exclusion of patients who smoked cigarettes (n = 15) or who had vascular disease (n = 4).In conclusion, this study shows that the plasma of Mexican-American subjects with NIDDM is more prone to lipid peroxidation than that of non-Hispanic whites.CONCLUSIONSIn conclusion, this study shows that the plasma of Mexican-American subjects with NIDDM is more prone to lipid peroxidation than that of non-Hispanic whites. Several lines of evidence support an atherogenic role for oxidized low-density lipoprotein (LDL). Studies on LDL oxidation in diabetes to date have examined LDL isolated from plasma, but have failed to evaluate the other pro- and antioxidant factors present in vivo, the balance of which could be crucial in determining the susceptibility of LDL to lipid peroxidation. We examined the oxidizability of plasma from Mexican-Americans in the San Antonio Heart Study. The oxidizability of plasma in 75 subjects with normal glucose tolerance (NGT), impaired glucose tolerance (IGT), and non-insulin-dependent diabetes mellitus (NIDDM) was studied after co-incubation with a free radical initiator, 2,2'-azobis-2-amidinopropane hydrochloride (AAPH). Lipid peroxide (LPO) levels were measured by a modified fluorimetric assay. Baseline LPO levels (mumol/l; means +/- SE) were similar in the three glucose tolerance categories (NGT, 1.99 +/- 0.07; IGT, 1.88 +/- 0.07; NIDDM, 1.97 +/- 0.07; P = 0.521). However, after incubation with AAPH (NGT, 4.30 +/- 0.20; IGT, 4.45 +/- 0.20; NIDDM, 5.35 +/- 0.20; P = 0.003), the diabetic plasma had significantly greater amounts of LPOs compared with the other two groups. There was no significant difference in LPOs between the NGT and IGT groups. The statistical significance of increased oxidizability of the diabetic plasma persisted after exclusion of patients who smoked cigarettes (n = 15) or who had vascular disease (n = 4). In conclusion, this study shows that the plasma of Mexican-American subjects with NIDDM is more prone to lipid peroxidation than that of non-Hispanic whites. |
Author | S M Haffner A Agil I Jialal M P Stern L Mykkanen |
Author_xml | – sequence: 1 givenname: Steven M surname: Haffner fullname: Haffner, Steven M organization: Division of Clinical Epidemiology, Department of Medicine, University of Texas Health Science Center at San Antonio San Antonio, Texas – sequence: 2 givenname: Ahmad surname: Agil fullname: Agil, Ahmad organization: Center for Human Nutrition and Laboratory of Molecular Pathology, Department of Pathology and Internal Medicine, University of Texas Southwestern Medical Center at Dallas Dallas, Texas – sequence: 3 givenname: Leena surname: Mykkanen fullname: Mykkanen, Leena organization: Division of Clinical Epidemiology, Department of Medicine, University of Texas Health Science Center at San Antonio San Antonio, Texas – sequence: 4 givenname: Michael P surname: Stern fullname: Stern, Michael P organization: Division of Clinical Epidemiology, Department of Medicine, University of Texas Health Science Center at San Antonio San Antonio, Texas – sequence: 5 givenname: Ishwarlal surname: Jialal fullname: Jialal, Ishwarlal organization: Center for Human Nutrition and Laboratory of Molecular Pathology, Department of Pathology and Internal Medicine, University of Texas Southwestern Medical Center at Dallas Dallas, Texas |
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Keywords | Endocrinopathy Human Lipoprotein LDL Metabolic disorder Pathophysiology Lipids Metabolic interrelation Oxidation Impaired glucose tolerance Non insulin dependent diabetes |
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Snippet | Plasma oxidizability in subjects with normal glucose tolerance, impaired glucose tolerance, and NIDDM.
S M Haffner ,
A Agil ,
L Mykkanen ,
M P Stern and
I... Several lines of evidence support an atherogenic role for oxidized low-density lipoprotein (LDL). Studies on LDL oxidation in diabetes to date have examined... |
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SubjectTerms | Amidines - pharmacology Biological and medical sciences Blood Glucose - metabolism Cholesterol - blood Cholesterol, HDL - blood Cholesterol, LDL - blood Diabetes Mellitus, Type 2 - blood Diabetes. Impaired glucose tolerance Diabetic Angiopathies - blood Endocrine pancreas. Apud cells (diseases) Endocrinopathies Ethnic Groups Etiopathogenesis. Screening. Investigations. Target tissue resistance European Continental Ancestry Group Female Glucose Intolerance - blood Glucose Tolerance Test Humans In Vitro Techniques Lipid Peroxidation - drug effects Lipid Peroxides - blood Male Medical sciences Mexican Americans Middle Aged Oxidation-Reduction Reference Values Sex Characteristics Texas Triglycerides - blood Vascular Diseases - blood |
Title | Plasma oxidizability in subjects with normal glucose tolerance, impaired glucose tolerance, and NIDDM |
URI | http://care.diabetesjournals.org/content/18/5/646.abstract https://www.ncbi.nlm.nih.gov/pubmed/8586002 https://www.proquest.com/docview/77539348 |
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