Abstract:Metabolic syndrome risk factors (MSRF) can lead to cardiovascular disease (CVD) and its prevalence is increasing at an alarming rate in the United States and worldwide. Pathways leading directly from visceral adiposity to the genesis of free fatty acids and lipid accumulation are mediators of insulin resistance and hypertension. These conditions lead to a proinflammatory and prothrombotic state that can potentiate cardiovascular disease. Metabolic syndrome risk factors are interrelated and associated with pred… Show more
“…18 In recent studies, 11,12 the use of CPB improved blood glucose, fructosamine, and HbA 1c levels in T2DM. These results are consistent with those reported in previous studies evaluating the efficacy of CP 8,9,[19][20][21] and biotin 22 in individuals with T2DM. 23,24 Glycemic control remains the cornerstone of therapeutic strategies in patients with T2DM and its complications.…”
Section: Discussionsupporting
confidence: 93%
“…In recent studies, 11,12 the use of CPB improved blood glucose, fructosamine, and HbA 1c levels in T2DM. These results are consistent with those reported in previous studies evaluating the efficacy of CP 8,9,19–21 and biotin 22 in individuals with T2DM 23,24 …”
Dyslipidemia, often found in type 2 diabetes mellitus (T2DM) patients, plays an important role in the progression of cardiometabolic syndrome. Two essential nutrients, chromium and biotin, may maintain optimal glycemic control. The authors report here a randomized, double-blind placebo-controlled trial (N=348; chromium picolinate and biotin combination [CPB]: 226, placebo: 122; T2DM participants with hemoglobin A1c [HbA1c] >or=7%) evaluating the effects of CPB on lipid and lipoprotein levels. Participants were randomly assigned (2:1 ratio) to receive either CPB (600 microg chromium as chromium picolinate and 2 mg biotin) or a matching placebo once daily for 90 days. Statistical analyses were conducted in all eligible participants. Subsequent supplemental analyses were performed in T2DM participants with hypercholesterolemia (HC) and in those using stable doses of statins. In the primary analysis, CPB lowered HbA1c (P<.05) and glucose (P<.02) significantly compared with the placebo group. No significant changes were observed in other lipid levels. In participants with HC and T2DM, significant changes in total cholesterol and low-density lipoprotein cholesterol (LDL-C) levels and atherogenic index were observed in the CPB group (P<.05). Significant decreases in LDL-C, total cholesterol, HbA1c , and very low-density cholesterol levels (P<.05) were observed in the CPB group taking statins. CPB treatment was well tolerated with no adverse effects, dissimilar from those associated with placebo. These data suggest that intervention with CPB improves cardiometabolic risk factors.
“…18 In recent studies, 11,12 the use of CPB improved blood glucose, fructosamine, and HbA 1c levels in T2DM. These results are consistent with those reported in previous studies evaluating the efficacy of CP 8,9,[19][20][21] and biotin 22 in individuals with T2DM. 23,24 Glycemic control remains the cornerstone of therapeutic strategies in patients with T2DM and its complications.…”
Section: Discussionsupporting
confidence: 93%
“…In recent studies, 11,12 the use of CPB improved blood glucose, fructosamine, and HbA 1c levels in T2DM. These results are consistent with those reported in previous studies evaluating the efficacy of CP 8,9,19–21 and biotin 22 in individuals with T2DM 23,24 …”
Dyslipidemia, often found in type 2 diabetes mellitus (T2DM) patients, plays an important role in the progression of cardiometabolic syndrome. Two essential nutrients, chromium and biotin, may maintain optimal glycemic control. The authors report here a randomized, double-blind placebo-controlled trial (N=348; chromium picolinate and biotin combination [CPB]: 226, placebo: 122; T2DM participants with hemoglobin A1c [HbA1c] >or=7%) evaluating the effects of CPB on lipid and lipoprotein levels. Participants were randomly assigned (2:1 ratio) to receive either CPB (600 microg chromium as chromium picolinate and 2 mg biotin) or a matching placebo once daily for 90 days. Statistical analyses were conducted in all eligible participants. Subsequent supplemental analyses were performed in T2DM participants with hypercholesterolemia (HC) and in those using stable doses of statins. In the primary analysis, CPB lowered HbA1c (P<.05) and glucose (P<.02) significantly compared with the placebo group. No significant changes were observed in other lipid levels. In participants with HC and T2DM, significant changes in total cholesterol and low-density lipoprotein cholesterol (LDL-C) levels and atherogenic index were observed in the CPB group (P<.05). Significant decreases in LDL-C, total cholesterol, HbA1c , and very low-density cholesterol levels (P<.05) were observed in the CPB group taking statins. CPB treatment was well tolerated with no adverse effects, dissimilar from those associated with placebo. These data suggest that intervention with CPB improves cardiometabolic risk factors.
“…In fact, CrPic showed multiple beneficial effects in T2DM, including attenuating body weight gain [3], improving lipid profiles [1][2][3][4][5][6], and enhancing endothelial function [4]. Chromium picolinate improves insulin sensitivity and may reduce other associated complications [7]. The mechanisms of CrPic action have remained obscure, despite multiple pathways of action being proposed, including a decrease in hepatic glucose production, an increase in peripheral glucose disposal, and a reduction of intestinal glucose absorption [8,9].…”
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