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1.
Exp Clin Endocrinol Diabetes ; 131(10): 508-514, 2023 Oct.
Article in English | MEDLINE | ID: mdl-37604165

ABSTRACT

INTRODUCTION: The current ultrasound scan classification system for thyroid nodules is time-consuming, labor-intensive, and subjective. Artificial intelligence (AI) has been shown to increase the accuracy of predicting the malignancy rate of thyroid nodules. This study aims to demonstrate the state-of-the-art Swin Transformer to classify thyroid nodules. MATERIALS AND METHODS: Ultrasound images were collected prospectively from patients who received fine needle aspiration biopsy for thyroid nodules from January 2016 to June 2021. One hundred thirty-nine patients with malignant thyroid nodules were enrolled, while 235 patients with benign nodules served as controls. Images were fed to Swin-T and ResNeSt50 models to classify the thyroid nodules. RESULTS: Patients with malignant nodules were younger and more likely male compared to those with benign nodules. The average sensitivity and specificity of Swin-T were 82.46% and 84.29%, respectively. The average sensitivity and specificity of ResNeSt50 were 72.51% and 77.14%, respectively. Receiver operating characteristics analysis revealed that the area under the curve of Swin-T was higher (AUC=0.91) than that of ResNeSt50 (AUC=0.82). The McNemar test evaluating the performance of these models showed that Swin-T had significantly better performance than ResNeSt50.Swin-T classifier can be a useful tool in helping shared decision-making between physicians and patients with thyroid nodules, particularly in those with high-risk characteristics of sonographic patterns.


Subject(s)
Deep Learning , Thyroid Neoplasms , Thyroid Nodule , Humans , Male , Thyroid Nodule/diagnostic imaging , Thyroid Nodule/pathology , Artificial Intelligence , Sensitivity and Specificity , Ultrasonography/methods , Thyroid Neoplasms/pathology
2.
Nutr Metab Cardiovasc Dis ; 32(7): 1725-1733, 2022 07.
Article in English | MEDLINE | ID: mdl-35527126

ABSTRACT

BACKGROUND AND AIMS: The primary goals of this study were to clarify 1) the effect of weight loss by lifestyle intervention on circulating total angiopoietin-like protein 8 (ANGPTL8), and 2) the role of physical activity on serum total ANGPTL8 in northern Americans with obesity but without diabetes. METHODS AND RESULTS: A total of 130 subjects with body mass index (BMI) â‰§ 35 kg/m2 but without diabetes were recruited, and 121 subjects completed a weight loss program for data analysis. Abdominal adipose tissue was determined by non-contrast computed tomography (CT). Serum total ANGPTL8 was higher in the group with obesity than in the lean control group. Serum total ANGPTL8 was positively correlated with waist circumference (WC), BMI, fasting insulin, HOMA-IR, HOMA-B, QUICKI, hs-CRP, IL-6, and leptin. Serum total ANGPTL8 did not significantly differ between the two intervention groups at baseline, and it was significantly lower after weight loss, with comparable changes with diet only and diet plus physical activity. CONCLUSION: Among northern Americans with obesity but without diabetes, a lifestyle modification resulted in significant reduction of circulating total ANGPTL8 concentrations in a 6-month weight-loss period. Although addition of physical activity resulted in greater total and liver fat loss, it did not promote further significant decline of serum total ANGPTL8 beyond diet alone.


Subject(s)
Peptide Hormones , Weight Reduction Programs , Angiopoietin-Like Protein 8 , Angiopoietin-like Proteins , Body Mass Index , Exercise , Humans , Obesity/diagnosis , Obesity/therapy , Prospective Studies , Weight Loss
3.
J Diabetes Investig ; 12(9): 1603-1609, 2021 Sep.
Article in English | MEDLINE | ID: mdl-33550691

ABSTRACT

AIMS/INTRODUCTION: The convergence of tuberculosis (TB) and diabetes mellitus (DM) is a new challenge in Asia as a result of the rising prevalence of diabetes mellitus with higher TB infection rates, and also because diabetes mellitus itself enhances TB disease activity and consequently the spread of TB. We aimed to address the risk presented by diabetes mellitus for TB infection. MATERIALS AND METHODS: Patients with diabetes mellitus were retrospectively recruited. The baseline assessments included age, sex, body mass index, fasting blood glucose, glycated hemoglobin, urine albumin-to-creatinine ratio and estimated glomerular filtration rate. TB was determined by meeting the international classification of disease, for TB diagnosis and receiving anti-TB treatment for at least 2 months. RESULTS: In total, 9,750 individuals with diabetes mellitus were recruited. The event rate of TB was 47 (0.48%). Younger age, lower proportion of men, higher fasting blood glucose and glycated hemoglobin values, and better renal function (estimated glomerular filtration rate and urine albumin-to-creatinine ratio) were observed in the metformin-exposed groups. Old age and male sex were associated with higher TB infection risk on multivariate analysis. Metformin users had a significantly lower risk for TB infection, whereas insulin users had a higher risk for TB infection. However, glycemic status had no effect on TB infection risk. CONCLUSIONS: This study provides clinical evidence from a survey of TB in individuals with diabetes mellitus. Old age, male sex and insulin use were risk factors for TB infection. Metformin remains the first choice of treatment for diabetes mellitus and has a potential protective effect against TB infection.


Subject(s)
Biomarkers/blood , Blood Glucose/analysis , Diabetes Mellitus/drug therapy , Hypoglycemic Agents/therapeutic use , Metformin/therapeutic use , Mycobacterium tuberculosis/drug effects , Tuberculosis/prevention & control , Aged , Diabetes Mellitus/microbiology , Diabetes Mellitus/pathology , Female , Follow-Up Studies , Glomerular Filtration Rate , Glycated Hemoglobin/analysis , Hospitals, Teaching , Humans , Kidney Function Tests , Longitudinal Studies , Male , Mycobacterium tuberculosis/isolation & purification , Prognosis , Retrospective Studies , Tuberculosis/microbiology
5.
PLoS One ; 14(11): e0224942, 2019.
Article in English | MEDLINE | ID: mdl-31770380

ABSTRACT

INTRODUCTION: Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disease in the western world and is highly associated with multiple cardiometabolic complications. The Zhejiang University (ZJU) index was first developed to predict NAFLD in Chinese populations, where it was shown to have better predictive value than other currently used indices. The aims of the present study were to 1) determine the diagnostic accuracy of ZJU index in identifying NAFLD in a well-phenotyped cohort of obese middle-aged American women and 2) compare its performance with other non-invasive indices for NAFLD identification. METHODS: To achieve this goal, we performed a retrospective analysis of a prospectively-collected cohort of participants enrolled in a weight loss trial for severe obesity (RENEW, clinicaltrials.gov identifier: NCT00712127). One hundred and seven women between the age of 30 and 55 with obesity class II (BMI 35-39.9 kg/m2) or class III (BMI ≥ 40 kg/m2) were recruited for analyses. Hepatic steatosis was measured using liver/spleen attenuation ratio (L/S ratio) from unenhanced abdominal computed tomography. Beside ZJU index, hepatic steatosis index (HSI), lipid accumulation production index (LAPI), and visceral adiposity index (VAI) were also determined and to compare their performance in predicting NAFLD. RESULTS: Of 107 obese women in the study, 40 (37.4%) met imaging criteria for NAFLD using cut-off value of L/S ratio < 1.1. The ZJU index was positively correlated with HIS, LAPI, but not VAI. The area under the curve was highest for the ZJU index (AUC = 0.742, 95% CI:0.647-0.837), followed by HSI (AUC = 0.728, 95% CI:0.631-0.825), LAPI (AUC = 0.682, CI:0.583-0.781), and VAI (AUC = 0.621, 95% CI:0.518-0.725), respectively, using the Youden method. CONCLUSION: The ZJU index is a powerful surrogate marker for NAFLD in severely obese western females and its predictive value was better than that of other commonly used indices for predicting NAFLD. Our study is the first to suggest that the ZJU index could be a promising model for use in western as well as Chinese populations.


Subject(s)
Biomarkers/metabolism , Non-alcoholic Fatty Liver Disease/complications , Non-alcoholic Fatty Liver Disease/metabolism , Obesity/complications , Adiposity , Adult , Female , Humans , Intra-Abdominal Fat/pathology , Lipids/chemistry , Middle Aged , North America , ROC Curve
7.
PLoS One ; 13(8): e0202280, 2018.
Article in English | MEDLINE | ID: mdl-30110378

ABSTRACT

INTRODUCTION: Postprandial hyperglycemia plays a pivotal role in cardiovascular disease. However, few studies have investigated associations between the severity of coronary artery disease (CAD) and postprandial glucose levels in angina patients without known diabetes before coronary angiography. METHODS: Subjects who were admitted for coronary angiography due to angina and were in stable condition after discharge were recruited. A standard 75-g oral glucose tolerance test (OGTT) was performed at outpatient visits approximately 2-4 weeks after hospital discharge, and fasting and post-challenge blood glucose were measured. Twenty-six volunteers in our hospital staff served as the healthy group. CAD severity was graded using the SYNTAX and Jeopardy scoring systems. RESULTS: The subjects in the angina group had a higher body mass index, higher fasting glucose, and higher 2-h postprandial glucose than those in the healthy group. The SYNTAX and Jeopardy scores were significantly associated with 2-h postprandial blood glucose (correlation coefficients = 0.164 and 0.187, respectively) but not with fasting glucose. Linear regression analyses revealed that SYNTAX and Jeopardy scores were independently associated with glucose levels at 120 min after OGTT (SYNTAX 95%CI = 0.003-0.103; Jeopardy score 0.002-0.027) but not with fasting glucose. CONCLUSION: CAD severity is associated with blood glucose levels after oral glucose challenge in patients without known diabetes before coronary angiography, suggesting that CAD patients should be routinely screened for post-challenge blood glucose.


Subject(s)
Angina Pectoris/blood , Angina Pectoris/complications , Blood Glucose , Coronary Artery Disease/blood , Coronary Artery Disease/complications , Hyperglycemia/blood , Adult , Angina Pectoris/diagnostic imaging , Body Mass Index , Coronary Angiography , Coronary Artery Disease/diagnostic imaging , Cross-Sectional Studies , Fasting/blood , Female , Glucose Tolerance Test , Humans , Hyperglycemia/complications , Male , Middle Aged , Postprandial Period , Severity of Illness Index
8.
Sci Rep ; 8(1): 7378, 2018 05 09.
Article in English | MEDLINE | ID: mdl-29743680

ABSTRACT

Endothelin-1 (ET-1) is associated with endothelial dysfunction and vasoconstriction. Increased circulating ET-1 levels are associated with long-term cardiovascular mortality. Renalase, released from kidney, metabolizes catecholamines and regulates blood pressure. An increase in circulating renalase levels has been reported in patients with chronic kidney disease (CKD) and is associated with coronary artery disease (CAD). We hypothesized the existence of a synergistic effect of serum renalase levels and CKD on ET-1 levels in patients with CAD. We evaluated 342 non-diabetic patients with established CAD. ET-1 and renalase levels were measured in all patients after an overnight fast. Patients with CKD had higher ET-1 (1.95 ± 0.77 vs. 1.62 ± 0.76 pg/ml, P < 0.001) and renalase levels (46.8 ± 17.1 vs. 33.9 ± 9.9 ng/ml, P < 0.001) than patients without CKD. Patients with both CKD and high renalase levels (>the median of 36.2 ng/ml) exhibited the highest serum ET-1 (P value for the trend <0.001). According to multivariate linear regression analysis, the combination of high serum renalase levels with CKD was a significant risk factor for increased serum ET-1 levels (regression coefficient = 0.297, 95% confidence interval = 0.063‒0.531, P = 0.013). In conclusion, our data suggest a synergistic effect of high serum renalase levels and CKD on increases in ET-1 levels in patients with established CAD.


Subject(s)
Coronary Artery Disease/complications , Endothelin-1/blood , Kidney/metabolism , Monoamine Oxidase/blood , Renal Insufficiency, Chronic/blood , Aged , Catecholamines/metabolism , Cross-Sectional Studies , Female , Humans , Kidney/enzymology , Male , Middle Aged , Monoamine Oxidase/metabolism , Renal Insufficiency, Chronic/complications , Renal Insufficiency, Chronic/metabolism
9.
Curr Med Res Opin ; 34(11): 1885-1892, 2018 11.
Article in English | MEDLINE | ID: mdl-29429368

ABSTRACT

OBJECTIVE: To investigate the effects of statins on all-cause mortality risk at different low-density lipoprotein cholesterol (LDL-C) levels, and to compare the mortality risk between statin users and non-users with identical LDL-C levels in a type 2 diabetes cohort. METHODS: In total, 10,582 outpatients aged ≥18 years with type 2 diabetes mellitus (T2DM) between 2009 and 2012 were enrolled in this retrospective cohort study in central Taiwan. All-cause mortality events were followed up until the end of 2014. According to the medical records during the follow-up period, the patients were classified into statin (+) and statin (-) groups. Patients were categorized into different LDL-C segments based on their mean LDL-C levels during the 2.8-year follow-up. RESULTS: Non-cardiovascular mortality accounted for more than half the deaths. Overall, statin therapy significantly reduced the all-cause mortality risk in both univariable and multivariable models (hazard ratios = 0.39 and 0.38, respectively). Sub-group analyses showed that the lowest mortality risk occurred in the 80-89 mg/dL segment in the statin (-) group and in the 90-99 mg/dL segment in the statin (+) group. Statin therapy significantly reduced the mortality risk at all LDL-C levels except for low LDL-C (<60 mg/dL). CONCLUSIONS: In addition to reducing LDL-C levels, statin therapy reduced all-cause mortality risk in Taiwanese patients with T2DM. Statins further reduced the mortality risk at most LDL levels. However, at low LDL-C levels, the positive effects of statins may have been nullified.


Subject(s)
Cholesterol, LDL/blood , Diabetes Mellitus, Type 2 , Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Hyperlipidemias , Adult , Aged , Asian People/statistics & numerical data , Cohort Studies , Diabetes Mellitus, Type 2/blood , Diabetes Mellitus, Type 2/mortality , Female , Humans , Hyperlipidemias/blood , Hyperlipidemias/drug therapy , Male , Middle Aged , Mortality , Proportional Hazards Models , Retrospective Studies , Taiwan/epidemiology
10.
Clin Chim Acta ; 476: 1-8, 2018 Jan.
Article in English | MEDLINE | ID: mdl-29080692

ABSTRACT

BACKGROUND: Arterial stiffening blunts postprandial vasodilatation. We hypothesized that brain-derived neurotrophic factor (BDNF) may modulate postprandial central pulse pressure, a surrogate marker for arterial stiffening. METHODS: A total of 82 non-diabetic subjects received a 75-g oral glucose tolerance test (OGTT) after overnight fasting. Serum BDNF concentrations were determined at 0, 30, and 120min to calculate the area under the curve (AUC). Brachial and central blood pressures were measured using a noninvasive central blood pressure monitor before blood withdrawals at 0 and 120min. RESULTS: With the median AUC of BDNF of 45(ng/ml)∗h as the cutoff value, the central pulse pressure after glucose intake was significantly higher in the subjects with a low BDNF than in those with a high BDNF (63±16 vs. 53±11mmHg, P=0.003), while the brachial pulse pressure was not significantly different between the 2 groups (P=0.099). In a multivariate linear regression model, a lower AUC of BDNF was an independent predictor of a higher central pulse pressure after oral glucose intake (linear regression coefficient-0.202, 95% confidence interval-0.340 to -0.065, P=0.004). CONCLUSION: After oral glucose challenge, a lower serum BDNF response is significantly associated with a higher central pulse pressure.


Subject(s)
Brain-Derived Neurotrophic Factor/blood , Glucose/administration & dosage , Administration, Oral , Aged , Aged, 80 and over , Blood Pressure , Fasting/blood , Female , Glucose Tolerance Test , Humans , Male , Middle Aged
11.
Medicine (Baltimore) ; 96(36): e7851, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28885336

ABSTRACT

Intraocular pressure is associated with metabolic syndrome. C-reactive protein (CRP) is associated with cardiovascular disease, irrespective of the presence of metabolic syndrome. In this study, we examined the synergistic effect of CRP and metabolic syndrome on intraocular pressure.A total of 1041 subjects were included for data analyses in this cross-sectional study. Intraocular pressure was measured using a noncontact tonometer, and serum CRP levels were measured using a commercially available kit.The intraocular pressure was significantly higher in the subjects with metabolic syndrome than in those without (14.1 ±â€Š3.0 vs 13.4 ±â€Š3.0 mm Hg, P = .002). Furthermore, intraocular pressures significantly increased according to CRP tertiles (13.1 ±â€Š3.0, 13.7 ±â€Š3.0, and 13.8 ±â€Š3.0 mm Hg from the lowest to highest tertile of CRP, respectively; P = .002). The highest intraocular pressure was observed in subjects with metabolic syndrome in the highest CRP tertile (P value for trend < .001). Multivariate linear regression analysis revealed that the influence of CRP was independent of metabolic syndrome and that high CRP levels were significantly associated with high intraocular pressure (95% confidence interval: 0.080-1.297, P = .027).In conclusion, systemic inflammation, reflected by serum CRP levels, is associated with high intraocular pressure in subjects with and without metabolic syndrome.


Subject(s)
C-Reactive Protein/analysis , Inflammation/epidemiology , Intraocular Pressure/physiology , Metabolic Syndrome/epidemiology , Adult , Age Factors , Cross-Sectional Studies , Female , Humans , Hypertension/epidemiology , Hypertriglyceridemia/epidemiology , Male , Middle Aged , Obesity , Risk Factors , Sex Factors , Smoking/epidemiology , Tonometry, Ocular
12.
Biomarkers ; 22(8): 798-804, 2017 Dec.
Article in English | MEDLINE | ID: mdl-28675064

ABSTRACT

CONTEXT: Inflammation is one of the mechanisms underlying cardiac syndrome X (CSX). OBJECTIVES: Few studies have compared the expression of inflammatory or adhesion molecules between coronary artery disease (CAD) versus CSX. MATERIALS AND METHODS: Ninety-two CSX and 145 CAD subjects without known diabetes mellitus underwent coronary angiogram for angina. RESULTS: Vascular cell adhesion molecule (VCAM)-1 (median, 507 versus 431 ng/ml, p = 0.001) was significantly higher in the CAD group. In the binary regression, VCAM-1 was a significant differential factor for CAD versus CSX. DISCUSSION AND CONCLUSION: Adhesion molecules might be implicated in the differential expression of macro versus microvascular coronary disease. TRIAL REGISTRATION NUMBER: NCT01198730 at https://clinicaltrials.gov.


Subject(s)
Biomarkers/blood , Coronary Artery Disease/blood , Diabetes Mellitus/blood , Microvascular Angina/blood , Vascular Cell Adhesion Molecule-1/blood , Aged , Coronary Angiography , Coronary Artery Disease/diagnosis , Cross-Sectional Studies , Diabetes Mellitus/diagnosis , Diagnosis, Differential , Female , Humans , Logistic Models , Male , Microvascular Angina/diagnosis , Middle Aged , ROC Curve , Retrospective Studies
13.
PLoS One ; 12(2): e0171753, 2017.
Article in English | MEDLINE | ID: mdl-28182722

ABSTRACT

INTRODUCTION: A high hemoglobin glycation index (HGI) and glycated hemoglobin (HbA1c) level are associated with greater inflammatory status, and dipeptidyl peptidase-4 (DPP-4) inhibitors can suppress inflammation. We aimed to evaluate the relationship between HGI and the therapeutic effect of DPP-4 inhibitors. METHODS: This retrospective cohort study followed 468 patients with type 2 diabetes receiving DPP-4 inhibitor treatment for 1 year. Estimated HbA1c was calculated using a linear regression equation derived from another 2969 randomly extracted patients with type 2 diabetes based on fasting plasma glucose (FPG) level. The subjects were divided into two groups based on HGI (HGI = observed HbA1c - estimated HbA1c). Mixed model repeated measures were used to compare the treatment efficacy after 1 year in patients with a low (HGI<0, n = 199) and high HGI (HGI≧0, n = 269). RESULTS: There were no significant group differences in mean changes of FPG after 1 year (-12.8 and -13.4 mg/dL in the low and high HGI groups, respectively). However, the patients with a high HGI had a significantly greater reduction in HbA1c from baseline compared to those with a low HGI (-1.9 versus -0.3% [-20.8 versus -3.3 mmol/mol]). Improvements in glycemic control were statistically significantly associated with the tested DPP-4 inhibitors in the high HGI group (-2.4, -1.4, -1.2 and -2.2% [-26.2, -15.3, -13.1 and -24.0 mmol/mol] for vildagliptin, linagliptin, saxagliptin and sitagliptin, respectively) but not in the low HGI group. CONCLUSIONS: The HGI index derived from FPG and HbA1c may be able to identify who will have a better response to DPP-4 inhibitors.


Subject(s)
Biomarkers, Pharmacological/blood , Diabetes Mellitus, Type 2/diagnosis , Diabetes Mellitus, Type 2/drug therapy , Dipeptidyl-Peptidase IV Inhibitors/therapeutic use , Glycated Hemoglobin/metabolism , Adamantane/analogs & derivatives , Adamantane/therapeutic use , Adult , Aged , Blood Glucose/drug effects , Diabetes Mellitus, Type 2/blood , Dipeptides/therapeutic use , Female , Glycated Hemoglobin/analysis , Health Status Indicators , Humans , Linagliptin/therapeutic use , Male , Middle Aged , Nitriles/therapeutic use , Predictive Value of Tests , Prognosis , Pyrrolidines/therapeutic use , Retrospective Studies , Sitagliptin Phosphate/therapeutic use , Treatment Outcome , Vildagliptin
14.
Clin Chim Acta ; 466: 194-200, 2017 Mar.
Article in English | MEDLINE | ID: mdl-28131673

ABSTRACT

BACKGROUND: Brain-derived neurotrophic factor (BDNF) is important for neural protection and energy homeostasis. In this study, we examined the effects of vascular cell adhesion molecule-1 (VCAM-1) and coronary artery disease (CAD) on BDNF. METHODS: Subjects who had undergone diagnostic angiography for angina were recruited, and a total of 240 subjects (144 with CAD and 96 without CAD) were enrolled. Serum BDNF was determined at 0, 30, and 120min during an oral glucose tolerance test (OGTT) to calculate the area under the curve (AUC) for BDNF. Serum VCAM-1 was determined at fasting. RESULTS: Significantly lower AUC of BDNF (42.8±10.7 vs. 47.4±11.7ng-h/ml, P=0.002) and higher serum VCAM-1 (583±383 vs. 482±171ng/ml, P=0.017) were noted in subjects with CAD compared to those without CAD. High VCAM-1 level was an independent predictor of low AUC of BDNF in subjects with and without CAD (95%CI between -0.011 and -0.002, P=0.008; -0.033 and -0.002, P=0.029, respectively). Serum BDNF was lowest in the CAD subjects with high VCAM-1 levels at all time points during OGTT. CONCLUSION: Our results showed that CAD was associated with low serum BDNF in response to OGTT, and VCAM-1 had a synergistic effect with CAD on the BDNF.


Subject(s)
Brain-Derived Neurotrophic Factor/blood , Coronary Artery Disease/blood , Vascular Cell Adhesion Molecule-1/blood , Angina Pectoris , Area Under Curve , Case-Control Studies , Glucose Tolerance Test , Humans , Predictive Value of Tests , Time Factors
15.
Medicine (Baltimore) ; 95(43): e5260, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27787389

ABSTRACT

Brain-derived neurotrophic factor (BDNF) plays a role in energy homeostasis. However, the postprandial BDNF change has not been well investigated. We hypothesized that the BDNF increment after oral glucose challenge is associated with body weight.To address this possibility, man adults with obesity in conjunction with metabolic syndrome were compared with normal weight controls at baseline in the initial cross-sectional protocol. The obese subjects then underwent a 12-week program for body-weight reduction in the prospective protocol. The area under the curve (AUC) of serum BDNF was recorded during a 75 g oral glucose tolerant test and the BDNF AUC index was defined as [(AUC of BDNF) - (fasting BDNF2 hours)]/(fasting BDNF2 hours).A total of 25 controls and 36 obese subjects completed the study assessments. In the cross-sectional protocol, the BDNF AUC index was significantly higher in the obese subjects than in the controls (9.0 ±â€Š16.5% vs. - 8.0 ±â€Š22.5%, P = 0.001). After weight reduction (from 97.0 ±â€Š12.5 kg to 88.6 ±â€Š12.9 kg, P < 0.001), the percentage change of body weight was significantly associated with the BDNF AUC index after the study (95% CI between 0.21 and 1.82, P = 0.015). Using 6% weight reduction as a cut-off value, a larger weight reduction was able to reliably predict a negative BDNF AUC index.In conclusion, a high BDNF AUC index was observed for obese men in this study, whereas the index value significantly decreased after body-weight reduction. These findings suggest that postprandial BDNF increment may be associated with obesity.


Subject(s)
Blood Glucose/metabolism , Body Weight , Brain-Derived Neurotrophic Factor/blood , Insulin Resistance/physiology , Metabolic Syndrome/blood , Obesity/complications , Adult , Aged , Cross-Sectional Studies , Fasting/blood , Follow-Up Studies , Glucose Tolerance Test , Humans , Male , Metabolic Syndrome/etiology , Metabolic Syndrome/physiopathology , Middle Aged , Obesity/blood , Obesity/physiopathology , Prospective Studies , Young Adult
16.
Clin Chim Acta ; 462: 55-59, 2016 Nov 01.
Article in English | MEDLINE | ID: mdl-27592367

ABSTRACT

BACKGROUND: Diabetic neuropathy is a common complication in patients with type 2 diabetes. However, the prevalence of painful diabetic polyneuropathy (PDPN) have been less studied. We examined the prevalence and risk factors of PDPN in outpatients with type 2 diabetes in an ethnic Chinese population. METHODS: This retrospective study enrolled 2358 outpatients with type 2 diabetes who had completed the Douleur Neuropathique en 4 Questions (DN4) questionnaire from January 2013 to October 2013. Patients with a total score ≥4 were defined as having PDPN. RESULTS: In all, 179 patients were diagnosed as having PDPN with a score of 4.49 on the DN4 questionnaire, compared with 0.66 for patients without PDPN. After adjusting the possible confounding factors, the risk of painful neuropathy was increased in the group without physical activity (Odds ratio 3.38, 95% CI 1.54-9.79), and in the group with macroalbuminuria (Odds ratio 2.31, 95% CI 1.44-3.73). Besides, there was a joint effect of macroalbuminuria and no physical activity habit on PDPN risk. CONCLUSIONS: The prevalence of PDPN was 7.6% among our outpatients with type 2 diabetes. Less physical activity and albuminuria, respectively, increased the risk of PDPN and had a joint effect.


Subject(s)
Albuminuria/epidemiology , Diabetes Mellitus, Type 2/epidemiology , Exercise , Pain/epidemiology , Peripheral Nervous System Diseases/epidemiology , Aged , Albuminuria/urine , China/ethnology , Diabetes Mellitus, Type 2/diagnosis , Female , Humans , Male , Middle Aged , Pain/diagnosis , Peripheral Nervous System Diseases/diagnosis , Taiwan/epidemiology
18.
Medicine (Baltimore) ; 94(42): e1802, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26496315

ABSTRACT

Type 2 diabetes mellitus (DM) is the most common single cause of end-stage renal disease. Albuminuria is the most commonly used marker to predict onset of diabetic nephropathy (DN) without enough sensitivity and specificity to detect early DN. This is the first study to identify urinary cyclophilin A (CypA) as a new biomarker for early DN.We recruited DM outpatients and healthy control subjects from January 2014 to December 2014. In this cross-sectional study, patients' urine samples were collected to determine the expression of urinary CypA. We also treated mesangial (MES-13) and tubular (HK-2) cells with glucose or free radicals to observe the expression of secreted CypA in Western blot analysis.A total of 100 DN patients and 20 healthy control subjects were enrolled. All variables were matched. In univariate analysis, the concentration of urinary CypA correlated well with the progression of renal function. A significant increase in urinary CypA was noted in stage 2 DN and persisted in later stages. We could diagnose stage 2 DN using urinary CypA with a sensitivity of 90.0% and specificity of 72.7%. The area under curve was up to 0.85, indicating a good discriminatory power. In cellular models, MES-13 and HK-2 cells can both release CypA.Urinary CypA is a good biomarker for early DN detection in humans and it can be released from either mesangial or tubular cells. The underlying molecular mechanisms still need further clarification in cellular and animal studies.


Subject(s)
Cyclophilin A/urine , Diabetic Nephropathies/urine , Adult , Biomarkers/urine , Cross-Sectional Studies , Female , Humans , Male , Middle Aged
19.
Clin Chem Lab Med ; 53(11): 1871-9, 2015 Oct.
Article in English | MEDLINE | ID: mdl-25816310

ABSTRACT

BACKGROUND: Low-density lipoprotein cholesterol (LDL-C) is an established risk factor for cardiovascular disease and is usually estimated by the Friedewald formula (FF) calculated from three parameters, namely, total cholesterol (TC), triglyceride (TG), and high-density lipoprotein cholesterol (HDL-C). We aimed to develop a new and simple formula (NF) for LDL-C estimation. METHODS: This cross-sectional study enrolled two study populations (a testing group, n=16,749, and a validation group, n=4940). Linear regression analysis was used in the testing group to investigate the association between measured LDL-C (mLDL-C) and TC concentration, and was verified in the validation group. RESULTS: The NF yielded an estimated LDL-C (eLDL-C) equal to 0.75 × total cholesterol-0.6465 (mmol/L). For the subjects with TC between 2.58 and 7.74 mmol/L, the difference between mLDL-C and eLDL-C using the NF was less than that from the FF (testing group: -0.04 to -0.20 vs. -0.28 to -0.38 mmol/L; validation group: 0.01 to -0.12 vs. -0.23 to -0.30 mmol/L; p<0.001, respectively). The predictability of the NF was not inferior to that of the FF in subjects with different triglyceride and HDL-C concentrations, and was not affected by diabetes diagnosis and statin use. However, the NF performed similar to or worse than the FF at TC concentrations <2.58 mmol/L and >7.74 mmol/L, respectively. CONCLUSIONS: In the Chinese population, the accuracy of eLDL-C measurement with the NF was better than that with the FF, especially in subjects with TC levels between 2.58 and 7.74 mmol/L. The NF is simple and may be used for screening as well as for follow-up of patients on lipid lowering agents.


Subject(s)
Asian People , Cholesterol, LDL/blood , Ethnicity , China/ethnology , Cross-Sectional Studies , Female , Humans , Linear Models , Male , Middle Aged
20.
Clin Chem Lab Med ; 53(4): 623-9, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25301674

ABSTRACT

BACKGROUND: Monocyte chemoattractant protein-1 (MCP-1) is involved in obesity-related renal injury. The aim of the present study was to examine the effects of weight loss on changes in MCP-1 and markers of renal injury, specifically serum cystatin C (S-CysC) and urinary N-acetyl glucosaminidase (UNAG), in obese people. METHODS: In this prospective study, 40 obese men with metabolic syndrome (MetS) participated in a 3-month dietary and exercise intervention. Twenty-eight subjects completed the study with a ≥5% weight loss. Circulating MCP-1, S-CysC and UNAG to creatinine ratio (UNCR) were determined before and after the weight loss program. RESULTS: Obesity-associated components of MetS demonstrated significant improvements after the weight loss program. In addition, at baseline, circulating MCP-1 concentrations were positively correlated with UNCR and S-CysC levels. After weight loss, blood MCP-1 and UNCR levels were significantly decreased, but S-CysC was not affected. Using multiple linear regression analysis, there was a significant relationship between changes in UNCR and MCP-1 after adjusting for other potential confounding factors. CONCLUSIONS: Weight loss may improve renal tubular injury by ameliorating obesity-related inflammation in obese men with MetS.


Subject(s)
Chemokine CCL2/blood , Kidney/injuries , Kidney/physiopathology , Metabolic Syndrome/complications , Obesity/complications , Obesity/physiopathology , Weight Loss , Acetylglucosaminidase/urine , Adult , Cystatin C/blood , Diet , Exercise , Humans , Male , Obesity/blood , Obesity/urine
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