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PMID |
Sentence |
1 |
19820014
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Fetuin-A inhibits the insulin receptor in vitro.
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2 |
20543523
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Fetuin-A inhibits insulin receptor autophosphorylation, which is mediated by its intrinsic tyrosine kinase activity.
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3 |
20543523
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Fetuin-A concentrations were also positively correlated with serum leptin (r = 0.150, p<0.01) and negatively with adiponectin concentrations (r = -0.208, p<0.001).
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4 |
20543523
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Stepwise regression analyses confirmed that the fetuin-A concentration was independently associated with the fasting insulin level and HOMA-IR, as were body mass index, triglyceride, LDL-cholesterol, leptin and adiponectin concentrations.
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5 |
20713686
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Higher serum fetuin-A was associated with abnormal albuminuria independent of BMI, waist circumference, homeostasis model assessment of insulin resistance, blood pressure, and other determinants of albuminuria in middle-aged and elderly Chinese women with NGT.
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6 |
20660040
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The liver-secreted protein Fetuin-A is elevated in insulin resistance, is an independent predictor of type 2 diabetes and is associated with atherosclerosis.
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7 |
20660040
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Delta (?) Fetuin-A concentrations correlated with ?fasting insulin (r = 0.710; P = 0.001), ?2-h insulin (r = 0.693; P = 0.005), and HOMA-insulin resistance (r = 0.684; P = 0.001).
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8 |
21085476
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Chemerin, progranulin, fetuin-A, and RBP4, IL-6, adiponectin and leptin serum concentrations were differentially regulated among the four investigated groups but only circulating chemerin was significantly different in patients with IGT compared to those with IFG.
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9 |
20501463
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On the other hand, aortic PWV inversely correlated with fetuin-A, log PTH, haemoglobin and albumin.
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10 |
20947626
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Moreover, the magnitude of cinacalcet-induced reduction in parathyroid hormone correlated with the decrease in RR but not with changes in serum or supernatant fetuin-A.
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11 |
20946008
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Fetuin-A has been associated with insulin resistance and inversely related with vascular calcification.
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12 |
20946008
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Serum fetuin-A concentration was not associated with measures of insulin resistance or with preclinical atherosclerosis in Hispanics and NHW.
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13 |
20199782
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Therefore, the maintenance of low levels of circulating fetuin-A may be a novel mechanism contributing to enhanced insulin sensitivity with regular physical activity.
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14 |
20716128
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Arterial calcification is the result of a complex interplay between stimulating (bone morphogenetic protein type 2 [BMP-2], RANKL) and inhibitory (matrix Gla protein, BMP-7, osteoprotegerin, fetuin-A, osteopontin) proteins.
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15 |
21087662
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Ahsg has a second physiological function in regulating how insulin signals through its receptor, a transmembrane tyrosine kinase.
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16 |
21087662
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Ahsg binds to tandem fibronectin type 3 (Fn3) domains present in the 194 amino acid residue extracellular portion of the ?-subunit of the insulin receptor, distant from the high-affinity pocket formed by two complementing ?-subunits where insulin binds.
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17 |
20185740
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Both weight loss and ezetimibe plus weight loss significantly (all P < 0.05) reduced body weight, visceral and subcutaneous adipose tissues, insulin resistance and plasma triglycerides, VLDL-apoB-100, apoC-III, fetuin-A, and retinol-binding protein-4 and increased plasma adiponectin concentrations.
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18 |
21556362
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The logistic regression analysis showed that fetuin-A were associated with elevated HOMA-IR and fasting serum insulin both among the participants with or without type 2 diabetes in the full adjusted analysis.
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19 |
21556362
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Higher fetuin-A concentrations were associated with type 2 diabetes and insulin resistance in middle aged and elderly Chinese.
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20 |
21226708
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Serum AHSG correlated negatively with adiponectin (r = -0·236, P = 0·006) even after adjusting for BMI (r = -0·177, P = 0·043).
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21 |
21226708
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Serum AHSG did not correlate significantly with CRP, resistin and TNF-? concentrations.
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22 |
21226708
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Association with adipokines favours the concept that AHSG is involved in atherosclerosis more likely through metabolic pathways (insulin resistance, obesity and adipocyte dysfunction) than by inflammation in patients with post-myocardial infarction.
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