2020•Zanco Journal of Medical SciencesOpen access

Serum Nesfatin-1 in patients with type 2 diabetes mellitus: A cross sectional study

Niyan Mohammad, Dler Qader Gallaly

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Abstract

IntroductionNesfatin-1 (NES-1) is a newly discovered multi-functional peptide hormone with an approximate molecular weight of 9.8 kilo Dalton and a half-life of 23.5 minutes.It was first discovered in 2006 by Oh-I and his coworkers.1-3 NES-1 is derived from nucleobindin2 (NUCB2) precursor, which is DNA and calcium binding protein that is found in the plasma membrane and neuroplasma.NUCB2 is highly conserved in humans, rats, and mice, that shares more than 85% of homology between humans and the other mammal species and even demonstrates similarities with lower organisms.[3][4][5] The NUCB2 precursor protein is possibly posttranslationally cleaved by the enzyme prohormone-convertase into the N-terminal NES-1amino acids 1-82 (AA 1-82), NES-2 (AA 85-163) and the C-terminal NES-3 (AA 166-396).1,6 Several biological actions for NES-1 have been identified, specifically of the middle part of it, which corresponds to AA 24-53, it has a key role in physiological effects of NES-1, particularly for an anorexic effect, whereas no biological action has been described for NES-2 and NES-3.6,7 NUCB2 and NES-1 are expressed by the central nervous system (CNS) and peripheral tissues.In CNS, expressed prominently in the Background and objective: Nesfatin-1 is a newly described peptide, derived from nucleobindin2.Nesfatin-1 suppresses food intake and it is involved in regulating insulin secretion.The aim of this study was to compare serum levels of Nesfatin-1 in patients having type 2 diabetes and non-diabetic subjects.Methods: This cross-sectional study included 90 participants; 64 patients with type 2 diabetes mellitus (32 males and 32 females) and 26 control subjects (13 males and 13 female).Body mass index, fasting serum level of glucose, fasting serum level of insulin, and glycated hemoglobin were estimated.Homeostasis model assessment of insulin resistance was calculated.Nesfatin-1 level was measured using enzyme-linked immunesorbent assay kit.The data was analyzed using Graphpad prism 7.04 for windows.Results: Type 2 diabetes patients aged from 33-78 years and the control group aged from 32-75 years.Nesfatin-1 level in the diabetic group was significantly lower than controls.The median interquartile range (IQR) of Nesfatin-1 was 0.765 (0.4-1.173) in diabetes and 1.02 (0.775-1.458) in controls.The diabetes group has significantly higher homeostasis model assessment of insulin resistance compared with non-diabetics.Serum Nesfatin-1 was correlated negatively with body mass index, fasting serum glucose, fasting serum insulin, glycatedhemoglobin, and homeostasis assessment of insulin resistance.Conclusion: Serum Nesfatin-1 level is negatively correlated with fasting serum glucose, fasting serum insulin, and glycated hemoglobin.This association supports the role of Nesfatin-1 in increased insulin resistance in patients with type 2 diabetes.

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IntroductionNesfatin-1 (NES-1) is a newly discovered multi-functional peptide hormone with an approximate molecular weight of 9.8 kilo Dalton and a half-life of 23.5 minutes.It was first discovered in 2006 by Oh-I and his coworkers.1-3 NES-1 is derived from nucleobindin2 (NUCB2) precursor, which is DNA and calcium binding protein that is found in the plasma membrane and neuroplasma.NUCB2 is highly conserved in humans, rats, and mice, that shares more than 85% of homology between humans and the other mammal species and even demonstrates similarities with lower organisms.[3][4][5] The NUCB2 precursor protein is possibly posttranslationally cleaved by the enzyme prohormone-convertase into the N-terminal NES-1amino acids 1-82 (AA 1-82), NES-2 (AA 85-163) and the C-terminal NES-3 (AA 166-396).1,6 Several biological actions for NES-1 have been identified, specifically of the middle part of it, which corresponds to AA 24-53, it has a key role in physiological effects of NES-1, particularly for an anorexic effect, whereas no biological action has been described for NES-2 and NES-3.6,7 NUCB2 and NES-1 are expressed by the central nervous system (CNS) and peripheral tissues.In CNS, expressed prominently in the Background and objective: Nesfatin-1 is a newly described peptide, derived from nucleobindin2.Nesfatin-1 suppresses food intake and it is involved in regulating insulin secretion.The aim of this study was to compare serum levels of Nesfatin-1 in patients having type 2 diabetes and non-diabetic subjects.Methods: This cross-sectional study included 90 participants; 64 patients with type 2 diabetes mellitus (32 males and 32 females) and 26 control subjects (13 males and 13 female).Body mass index, fasting serum level of glucose, fasting serum level of insulin, and glycated hemoglobin were estimated.Homeostasis model assessment of insulin resistance was calculated.Nesfatin-1 level was measured using enzyme-linked immunesorbent assay kit.The data was analyzed using Graphpad prism 7.04 for windows.Results: Type 2 diabetes patients aged from 33-78 years and the control group aged from 32-75 years.Nesfatin-1 level in the diabetic group was significantly lower than controls.The median interquartile range (IQR) of Nesfatin-1 was 0.765 (0.4-1.173) in diabetes and 1.02 (0.775-1.458) in controls.The diabetes group has significantly higher homeostasis model assessment of insulin resistance compared with non-diabetics.Serum Nesfatin-1 was correlated negatively with body mass index, fasting serum glucose, fasting serum insulin, glycatedhemoglobin, and homeostasis assessment of insulin resistance.Conclusion: Serum Nesfatin-1 level is negatively correlated with fasting serum glucose, fasting serum insulin, and glycated hemoglobin.This association supports the role of Nesfatin-1 in increased insulin resistance in patients with type 2 diabetes.

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Available abstract

IntroductionNesfatin-1 (NES-1) is a newly discovered multi-functional peptide hormone with an approximate molecular weight of 9.8 kilo Dalton and a half-life of 23.5 minutes.It was first discovered in 2006 by Oh-I and his coworkers.1-3 NES-1 is derived from nucleobindin2 (NUCB2) precursor, which is DNA and calcium binding protein that is found in the plasma membrane and neuroplasma.NUCB2 is highly conserved in humans, rats, and mice, that shares more than 85% of homology between humans and the other mammal species and even demonstrates similarities with lower organisms.[3][4][5] The NUCB2 precursor protein is possibly posttranslationally cleaved by the enzyme prohormone-convertase into the N-terminal NES-1amino acids 1-82 (AA 1-82), NES-2 (AA 85-163) and the C-terminal NES-3 (AA 166-396).1,6 Several biological actions for NES-1 have been identified, specifically of the middle part of it, which corresponds to AA 24-53, it has a key role in physiological effects of NES-1, particularly for an anorexic effect, whereas no biological action has been described for NES-2 and NES-3.6,7 NUCB2 and NES-1 are expressed by the central nervous system (CNS) and peripheral tissues.In CNS, expressed prominently in the Background and objective: Nesfatin-1 is a newly described peptide, derived from nucleobindin2.Nesfatin-1 suppresses food intake and it is involved in regulating insulin secretion.The aim of this study was to compare serum levels of Nesfatin-1 in patients having type 2 diabetes and non-diabetic subjects.Methods: This cross-sectional study included 90 participants; 64 patients with type 2 diabetes mellitus (32 males and 32 females) and 26 control subjects (13 males and 13 female).Body mass index, fasting serum level of glucose, fasting serum level of insulin, and glycated hemoglobin were estimated.Homeostasis model assessment of insulin resistance was calculated.Nesfatin-1 level was measured using enzyme-linked immunesorbent assay kit.The data was analyzed using Graphpad prism 7.04 for windows.Results: Type 2 diabetes patients aged from 33-78 years and the control group aged from 32-75 years.Nesfatin-1 level in the diabetic group was significantly lower than controls.The median interquartile range (IQR) of Nesfatin-1 was 0.765 (0.4-1.173) in diabetes and 1.02 (0.775-1.458) in controls.The diabetes group has significantly higher homeostasis model assessment of insulin resistance compared with non-diabetics.Serum Nesfatin-1 was correlated negatively with body mass index, fasting serum glucose, fasting serum insulin, glycatedhemoglobin, and homeostasis assessment of insulin resistance.Conclusion: Serum Nesfatin-1 level is negatively correlated with fasting serum glucose, fasting serum insulin, and glycated hemoglobin.This association supports the role of Nesfatin-1 in increased insulin resistance in patients with type 2 diabetes.

Key concepts: Medicine, Prohormone, Endocrinology, Diabetes mellitus, Prohormone convertase, Internal medicine, Hormone, Insulin

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Serum Nesfatin-1 in patients with type 2 diabetes mellitus: A cross sectional study — Research Paper | ScholarLens