2007
DOI: 10.1016/j.diabres.2006.07.031
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Plasma visfatin levels in patients with newly diagnosed and untreated type 2 diabetes mellitus and impaired glucose tolerance

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Cited by 177 publications
(147 citation statements)
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“…In humans, the normal fasting PBEF level is 10-40 ng/ml [1][2][3][4][5], which equals 180-700 pmol/l for this 55 kDa protein, 3.6-14 times the concentration of the normal fasting insulin level (50 pmol/l). If PBEF could act with the same efficacy as insulin [1], it should contribute importantly to the regulation of glucose metabolism.…”
Section: Discussionmentioning
confidence: 94%
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“…In humans, the normal fasting PBEF level is 10-40 ng/ml [1][2][3][4][5], which equals 180-700 pmol/l for this 55 kDa protein, 3.6-14 times the concentration of the normal fasting insulin level (50 pmol/l). If PBEF could act with the same efficacy as insulin [1], it should contribute importantly to the regulation of glucose metabolism.…”
Section: Discussionmentioning
confidence: 94%
“…Visfatin was also shown to mimic the effect of insulin with the same efficacy in rodent cells in vitro and in mouse models [1]. However, subsequent studies in human subjects reported conflicting results with regard to its relation with adiposity [2][3][4], subcutaneous or visceral fat [2,3], and insulin resistance [3][4][5], suggesting that the role of this protein in the development of obesity and insulin resistance remains unclear.…”
Section: Introductionmentioning
confidence: 99%
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“…Visfatin levels increased in Asian Indians with type 2 diabetes mellitus, but the association was lost after adjusting for obesity [10]. In another study, visfatin levels were reported to be higher in the diabetic group than the controls, but there was no significant difference in visfatin levels between the impaired glucose-tolerant group and the healthy controls [11]. Visfatin levels were correlated with HbA1c in patients with type 2 diabetes and lowered by intensive glycemic control [12].…”
Section: Introductionmentioning
confidence: 89%
“…It has been shown that visfatin binds to the insulin receptor at a distinct site, and exerts its hypoglycemic activity by reducing glucose release from hepatocytes, and stimulating glucose utilization in peripheral tissues (6). The synthesis and secretion of visfatin are shown to be up-regulated in several animal models of obesity, as well as human with abdominal obesity and/or type 2 diabetes mellitus (7)(8)(9).…”
Section: Introductionmentioning
confidence: 99%