Association of serum Sestrin2 level with metabolic risk factors in newly diagnosed drug-naïve type 2 diabetes. (October 2018)
- Record Type:
- Journal Article
- Title:
- Association of serum Sestrin2 level with metabolic risk factors in newly diagnosed drug-naïve type 2 diabetes. (October 2018)
- Main Title:
- Association of serum Sestrin2 level with metabolic risk factors in newly diagnosed drug-naïve type 2 diabetes
- Authors:
- Chung, Hye Soo
Hwang, Hwan-Jin
Hwang, Soon Young
Kim, Nam Hoon
Seo, Ji A.
Kim, Sin Gon
Kim, Nan Hee
Baik, Sei Hyun
Choi, Kyung Mook
Yoo, Hye Jin - Abstract:
- Highlights: Sesn2 level demonstrates a trend of increasing in subjects with metabolic syndrome. Sesn2 level has significant positive correlations with metabolic risk factors. In diabetes, Sesn2 level was associated with insulin resistance and body composition. Abstract: Aims: Previous in-vitro and in-vivo experimental studies have shown that Sestrin2 attenuates oxidative stress and the pro-inflammatory pathway, resulting in improving metabolic homeostasis. However, the relationship between circulating Sestrin2 concentration and cardiometabolic risks in humans has not been explored. Methods: Sestrin2 concentration was measured in 240 subjects (46 without diabetes and 194 with diabetes), and the associations between Sestrin2 level and various cardiometabolic risk factors including body composition, insulin resistance, and atherosclerosis was assessed. Results: Sestrin2 concentration showed a trend of increasing in subjects with metabolic syndrome. After adjustment for age and gender, Sestrin2 level had a positive relationship with serum triglyceride, alanine aminotransferase (ALT), and creatinine levels, but no association with carotid atherosclerosis. Especially, in subjects with type 2 diabetes Sestrin2 concentration exhibited a significant positive correlation with body mass index ( P = 0.015), waist circumference ( P = 0.020), high-sensitivity C-reactive protein ( P = 0.008), Homeostatic Model Assessment of Insulin Resistance (HOMA-IR) ( P = 0.041), percentage body fatHighlights: Sesn2 level demonstrates a trend of increasing in subjects with metabolic syndrome. Sesn2 level has significant positive correlations with metabolic risk factors. In diabetes, Sesn2 level was associated with insulin resistance and body composition. Abstract: Aims: Previous in-vitro and in-vivo experimental studies have shown that Sestrin2 attenuates oxidative stress and the pro-inflammatory pathway, resulting in improving metabolic homeostasis. However, the relationship between circulating Sestrin2 concentration and cardiometabolic risks in humans has not been explored. Methods: Sestrin2 concentration was measured in 240 subjects (46 without diabetes and 194 with diabetes), and the associations between Sestrin2 level and various cardiometabolic risk factors including body composition, insulin resistance, and atherosclerosis was assessed. Results: Sestrin2 concentration showed a trend of increasing in subjects with metabolic syndrome. After adjustment for age and gender, Sestrin2 level had a positive relationship with serum triglyceride, alanine aminotransferase (ALT), and creatinine levels, but no association with carotid atherosclerosis. Especially, in subjects with type 2 diabetes Sestrin2 concentration exhibited a significant positive correlation with body mass index ( P = 0.015), waist circumference ( P = 0.020), high-sensitivity C-reactive protein ( P = 0.008), Homeostatic Model Assessment of Insulin Resistance (HOMA-IR) ( P = 0.041), percentage body fat ( P = 0.001), and truncal fat mass ( P = 0.005) after adjusting age and gender. Multiple stepwise regression analysis identified age, serum ALT and creatinine levels, and percentage body fat as independent determining factors for Sestrin2 concentration in patients with type 2 diabetes ( R 2 = 0.173). Conclusions: This study is the first to demonstrate a trend for increased Sestrin2 level in subjects with metabolic syndrome. In particular, in subjects with type 2 diabetes, Sestrin2 was significantly related to insulin resistance and percentage body fat, suggesting its potential as a novel modulatory factor for metabolic disorders in humans. … (more)
- Is Part Of:
- Diabetes research and clinical practice. Volume 144(2018)
- Journal:
- Diabetes research and clinical practice
- Issue:
- Volume 144(2018)
- Issue Display:
- Volume 144, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 144
- Issue:
- 2018
- Issue Sort Value:
- 2018-0144-2018-0000
- Page Start:
- 34
- Page End:
- 41
- Publication Date:
- 2018-10
- Subjects:
- ALT alanine aminotransferase -- AMPK AMP-dependent protein kinase -- ANOVA analysis of variance -- AST aspartate aminotransferase -- baPWV brachial-ankle pulse wave velocity -- BMI body mass index -- BUN blood urea nitrogen -- CIMT carotid intima-media thickness -- CV coefficient of variation -- CVD cardiovascular disease -- DBP diastolic blood pressure -- DSCF Dwass, Steel, Critchlow-Fligner -- DXA dual-energy X-ray absorptiometry -- ELISA enzyme-linked immunosorbent assay -- ER endoplasmic reticulum -- ESC European Society of Cardiology -- ESH European Society of Hypertension -- FPG fasting plasma glucose -- HbA1c hemoglobin A1c -- HDL high-density lipoprotein -- HOMA-IR homeostatic model assessment of insulin resistance -- hsCRP high-sensitivity C-reactive protein -- KGDP Korea Guro Diabetes Program -- mTORC1 mammalian target of rapamycin complex 1 -- PET positron emission tomography -- PI3K phosphatidylinositol-3-kinase -- SBP systolic blood pressure -- Sesn2 Sestrin2 -- TBR target-to-background ratio -- UCP1 uncoupling protein 1 -- WC waist circumference -- WHR waist-to-hip ratio
Sestrin2 -- Type 2 diabetes mellitus -- Metabolic syndrome -- Atherosclerosis
Diabetes -- Periodicals
Diabetes Mellitus -- Periodicals
616.462 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01688227 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01688227 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01688227 ↗
http://www.sciencedirect.com/science/journal/01688227 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.diabres.2018.07.024 ↗
- Languages:
- English
- ISSNs:
- 0168-8227
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - 3579.603700
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