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Lipoprotein abnormalities and their consequences for patients with Type 2 diabetes
Abstract
Dyslipidaemia is common in patients with Type 2 diabetes and is held to be responsible for considerable CVD-related morbidity and mortality. Patients with Type 2 diabetes are at high risk from complications associated with atherosclerosis and should therefore receive preventive interventions. At the level of the adipocyte, impaired insulin action leads to increased rates of intracellular hydrolysis of triglycerides with the release of NEFA. The rise in NEFA provides substrate for the liver that, in the presence of impaired insulin action and relative insulin deficiency, is associated with complex alterations in plasma lipids: * Plasma VLDL levels are raised. (i). Increased VLDL levels are associated with post-prandial hyperlipidaemia that is compounded by impaired LPL activity. The latter may be independently associated with CAD. (ii). Remnant particles can deliver more cholesterol to macrophages than LDL-C particles. Thrombogenic alterations in the coagulation system also ensue from hypertriglyceridaemia. * Plasma HDL-C levels are reduced. (i). The reduction in cardioprotective HDL-C means a reduction of cholesterol efflux from the tissues--the first step in reverse cholesterol transport to the liver from peripheral tissues. (ii). The antioxidant and antiatherogenic activities of HDL-C are reduced when circulating levels are low. * LDL-C particles become small and dense. Small, dense LDL-C particles are held to be more atherogenic than their larger, buoyant counterparts because they (a) are more liable to oxidation and (b) may more readily adhere to and subsequently invade the arterial wall. The atherogenicity of LDL-C may also be enhanced by nonenzymatic glycation. Metabolic and lipid abnormalities can often be improved with lifestyle changes, including dietary modification, weight loss, smoking cessation and increased exercise. Although attainment of better glycaemic control may improve diabetic dyslipidaemia, pharmacological intervention is usually required. Several large-scale clinical trials, including 4S and more recently HPS, have clearly demonstrated the benefits of statins in reducing cardiovascular events. By virtue of their high absolute risk of CVD, many patients with Type 2 diabetes may achieve a greater risk reduction than their non-diabetic counterparts. For example, in 4S there was a 43% reduction in total mortality risk among patients with diabetes compared with 29% for non-diabetics and a reduced risk of MI by 55% vs. 32% for diabetic and non-diabetics, respectively. In the diabetic subgroup in HPS, there were reductions of approximately 25-30% in the risk of first major vascular events. More recently, the lipid-lowering arm of the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT) was halted early because of a significant reduction in cardiovascular events compared with placebo. Surprisingly an analysis of subgroups failed to show significance among the diabetic population, although the sample size, shortened follow-up period and higher drop-in statin use among diabetics on placebo may have affected results. The Collaborative Atorvastatin Diabetes Study (CARDS), involving 2800 patients with Type 2 diabetes, was halted 2 years early in June 2003 because patients allocated atorvastatin had significant reductions in MI, stroke and surgical procedures compared with those receiving placebo. The UKPDS demonstrated that the appearance and progression of certain microvascular complications of Type 2 diabetes could be reduced by treatment directed at hyperglycaemia and hypertension. In addition, correction of dyslipidaemia in patients with diabetes is important in reducing the high toll from macrovascular disease. The subjects in the HPS had similar lipid profiles to the participants in UKPDS, suggesting that additional benefit would accrue from a therapeutic assault on the main cardiovascular risk factors simultaneously. We now have firm evidence that appropriate use of statins in patients with Type 2 diabetes can significantly reduce cardiovascular morbidity and mortality.
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“Since elevated plasma glucose, lipids, and lipid oxidation have been associated with coronary artery disease (CAD),52,53 these data suggest the potential role of edible berries in ameliorating these risk factors.”
From Berries: emerging impact on cardiovascular health (2010) · cites this paper as [52]
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“T Patients with T2DM are susceptible to metabolic complications including dyslipidemia, increased inflammatory markers [28], oxidative stress, and hypertension [3].”
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“It is prevalent in patients with T2DM and is believed to be the major cause of considerable CVD-related morbidity and mortality [14, 15].”
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“Diet Baseline mean (SD) Final mean (SD) Difference (95% CI) 𝑃𝑃 value Total cholesterol (mmol/L) Almond 5.88 (0.66) 5.55 (0.65) −0.14 (−0.29, 0.01) 0.073 Sun�ower kernel 6.11 (0.68) 5.56 (0.59) HDL cholesterol (mmol/L) Almond 1.27 (0.32) 1.26 (0.31) −0.04 (−0.085, −0.001) 0.045 Sun�ower kernel 1.32 (0.33) 1.25 (0.31) T…”
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Role of SN1 Lipases on Plasma Lipids in Metabolic Syndrome and Obesity
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“Lower LPL activity has been associated with severe hypertriglyceridemia accompanied by low levels of high-density lipoprotein–cholesterol (HDL-C).(3,4) HL is involved in HDL metabolism as well as being responsible for the metabolism of apolipoprotein B–containing lipoproteins (especially intermediate-density lipoprote…”
Extended-release niacin with laropiprant: a review on efficacy, clinical effectiveness and safety
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“The sdLDL is more susceptible to oxidation and glycation compared with more buoyant LDL; hence it is assumed to be more atherogenic [76-78].”
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Current pharmacotherapeutic concepts for the treatment of cardiovascular disease in diabetics
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“These small LDL particles that occupy the vessel wall are easier to oxidize and extremely atherogenic [Koba et al. 2008; Hayashi et al. 2007; Krentz 2003; Goldberg 2001].”
BackgroundAttenuation of Some Metabolic Deteriorations Induced by Diabetes Mellitus Using Carnosine
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“Diabetes mellitus often involves abnormal lipid metabolism which causes complications in diabetic subjects (Krentz, 2003).”
BackgroundLipid profile among diabetes patients in Gaborone, Botswana
Mengesha, A. Y. (2006) · Journal of Endocrinology Metabolism and Diabetes of South Africa · doi:10.1080/22201009.2006.10872137 · Cited by 24
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“Height, weight, body mass index (BMI), waist, systolic blood pressure (SBP), diastolic blood pressure (DBP), fasting blood glucose, HbA1c, total cholesterol (TC), triglyceride (TG), high density lipoprotein cholesterol (HDL), low density lipoprotein cholesterol (LDL), and creatinine of samples were determined (Table 1…”
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“It is transported by LDLs to the tissues, which means that lower LDL levels (for instance, because of statin therapy) can lead to less a -to- copherol delivered to the tissues [76].”
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Association among Microalbuminuria and Oxidative Stress Biomarkers in Patients with Type 2 Diabetes
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“Moreover, the altered concentrations of lipoproteins are also found in glomerulopathy or chronic renal failure.(33) Interestingly, in our study, we observed a linear relationship between LDL cholesterol and microalbuminuria.”
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“with diabetes mellitus by the sheer presence of hyperglycaemia [6].”
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Models for Changing Patient Behavior
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Effective care of patients with type 2 diabetes and dyslipidemia: A nurse's perspective
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“It often involved abnormal lipid metabolism which is metabolic disorder in diabetic complications (Bansal et al., 2012; Krentz, 2003).”
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“[25] Small, dense LDL particles are considered more atherogenic than the larger, buoyant LDL particles because they are more readily oxidized and glycated, which make them more likely to invade the arterial wall.[26,27] This can initiate atherosclerosis or lead to increased migration and apoptosis of vascular smooth m…”
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Metadata
- Authors
- Krentz, A. J.
- Affiliations
- Southampton General Hospital (GB)
- Corresponding author
- Krentz, Andrew J
- ORCID
- Krentz, Andrew J
- Venue
- Diabetes Obesity and Metabolism
- Publisher
- Wiley
- Published
- 2003-10-22
- Volume
- 5
- Issue
- s1
- Pages
- S19-27
- ISSN
- 1462-8902 (ISSN-L)
- 1463-1326
- OpenAlex
- W2117545273
- Cited by
- 205
- References
- 56
- Citations by year
- 2025: 3 · 2024: 2 · 2023: 7 · 2022: 5 · 2021: 7 · 2020: 7 · 2019: 4 · 2018: 5 · 2017: 9 · 2016: 12 · 2015: 10 · 2014: 21 · 2013: 10 · 2012: 14
- FWCI
- 1.66
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Diabetes Obesity and Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipoproteins and Cardiovascular Health
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipid metabolism and disorders
- Keywords
- type 2 diabetes, dyslipidemia, cardiovascular disease, atherosclerosis, hypertriglyceridemia, small dense LDL, HDL cholesterol, remnant lipoproteins, lipoprotein lipase, VLDL, glycation, statins, lifestyle modification, reverse cholesterol transport, coronary artery disease, thrombosis
- MeSH terms
- Coronary Artery Disease, Diabetes Mellitus, Type 2, Diabetic Angiopathies, Humans, Hyperlipidemias, Insulin Resistance, Cholesterol, HDL, Cholesterol, LDL, Risk Factors, Hypertriglyceridemia, Randomized Controlled Trials as Topic
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