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1.
BMC Nephrol ; 22(1): 182, 2021 05 19.
Article in English | MEDLINE | ID: mdl-34011292

ABSTRACT

BACKGROUND: The hypertriglyceridemic waist (HTGW) phenotype has been proposed to be related to the occurrence and progression of chronic kidney disease (CKD). The ageing trend of the Chinese population continues to intensify, and elderly individuals are at high risk of CKD. The purpose of this study was to investigate the cross-sectional and longitudinal associations between the HTGW phenotype and the risk of CKD by following community-dwelling adults aged 60 years and older in Tianjin, China, for 7 years. METHODS: This study was an observational cohort study conducted between 2013 and 2019. Of 2050 participants aged 60 years and older who underwent an annual health examination in 2013, 1605 individuals with complete data were enrolled in the cross-sectional analysis. Among them, 1271 individuals were observed until 2019. Detailed follow-up records were available for 816 participants, of whom 600 participants without CKD at baseline were eligible for inclusion in the retrospective analysis. The HTGW phenotype was defined as a waist circumference of 90 cm or more and triglyceride concentrations of 2.0 mmol/L or more in males or a waist circumference of 85 cm or more and triglyceride concentrations of 1.5 mmol/L or more in females. CKD was defined as an estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73m2 and/or proteinuria (urinary albumin-to-creatinine ratio (ACR) ≥ 30 mg/g). Multivariable logistic regression analyses were performed to evaluate the relationship between the HTGW phenotype and CKD. RESULTS: In 2013, the prevalence of CKD among older adults was 31.03%, and the prevalence of CKD in the HTGW phenotype group was 37.81%. Over a 7-year observation period, 195 individuals developed CKD, with an incidence rate of 32.50%. Statistically significant associations were observed between the HTGW phenotype and CKD in older adults in both cross-sectional surveys and retrospective analyses, with odds ratios and 95% confidence intervals of 1.38 (95% CI: 1.03-1.86, P = 0.033) and 2.27 (95% CI: 1.30-3.97, P = 0.004), respectively, after adjustment for confounders. CONCLUSIONS: In this community-based cohort study, the HTGW phenotype was confirmed to be independently associated with an increased risk of prevalent and incident CKD in older adults aged 60 years and above in Tianjin, China.


Subject(s)
Hypertriglyceridemic Waist/complications , Renal Insufficiency, Chronic/etiology , Triglycerides/blood , Waist Circumference , Aged , Aged, 80 and over , China/epidemiology , Cohort Studies , Cross-Sectional Studies , Female , Glomerular Filtration Rate , Humans , Independent Living , Male , Middle Aged , Phenotype , Prevalence , Renal Insufficiency, Chronic/epidemiology , Risk Factors
2.
Ren Fail ; 41(1): 946-953, 2019 Nov.
Article in English | MEDLINE | ID: mdl-31599192

ABSTRACT

Objective: Despite the achievement of blood glucose, blood pressure targets, the risk for kidney injury remains high among older adults. This observational retrospective study investigated whether high TG or high WC contribute to this high residual risk for kidney injury. Methods: A total of 843 elderly from Dongli Community, Tianjin, China, we selected 666 individuals with a baseline estimated glomerular filtration rate (eGFR) ≥60 mL/min/1.73 m2 and negative microalbuminuria completing a 3-year follow-up. At baseline, subjects were grouped according to the levels of TG and WC. The primary outcome was the incidence of kidney injury, defined as low eGFR (eGFR <60 mL/min/1.73 m2) or reduced eGFR (eGFR reduced >25%) or UACR ≥30 mg/g. Results: Overall, 6.01% developed low eGFR, 11.11% reduced eGFR, 25.98% UACR ≥30 mg/g, and 3.45% low eGFR and UACR ≥30mg/g after 3-year follow-up. TG ≥1.7 mmol/L increased the risk of eGFR <60 mL/min/1.73 m2 by 1.44-fold, of UACR ≥30 mg/g by 32%, and of developing both abnormality by 1.41-fold in model 1; further adjustment for potential confounders factors, the association is slightly weakened in model 2 and 3; WC (≥90 cm in men and ≥85 cm in women) were associated with a 1.68-fold higher risk of eGFR <60 mL/min/1.73 m2 and a 1.43-fold risk of UACR ≥30 mg/g and a 1.89-fold risk of developing both abnormality in model 1. Further adjustment for potential confounders factors, the association is slightly weakened in model 2 and 3. Conclusions: In a population of Chinese community-dwelling older adults, high TG and central obesity were risk factors for the development of kidney injury over 3 years.


Subject(s)
Obesity, Abdominal/epidemiology , Renal Insufficiency, Chronic/epidemiology , Triglycerides/blood , Age Factors , Aged , China/epidemiology , Creatinine/blood , Disease Progression , Female , Follow-Up Studies , Glomerular Filtration Rate , Humans , Incidence , Independent Living , Male , Middle Aged , Obesity, Abdominal/diagnosis , Renal Insufficiency, Chronic/blood , Renal Insufficiency, Chronic/diagnosis , Retrospective Studies , Risk Factors , Waist Circumference
3.
Scand J Clin Lab Invest ; 75(3): 273-81, 2015 May.
Article in English | MEDLINE | ID: mdl-25723617

ABSTRACT

BACKGROUND: Previous studies demonstrated that men with type 2 diabetes mellitus (T2DM) had significantly lower serum prostate-specific antigen (PSA) levels than healthy men. However, the influence of prediabetes (preDM) on serum PSA levels is unknown. The aim of this study was to investigate the relationships between preDM and serum PSA levels. METHODS: A cross-sectional analysis was conducted to determine the relationships between preDM and serum PSA levels. Data were obtained from men over 50 years of age who measured serum PSA levels in the physical examination center of Tianjin Union Medical Center from May to July 2014. Pearson's correlation analysis and multivariable linear regression analysis were utilized to calculate the correlations between PSA levels and various clinical and biochemical variables. RESULTS: In age-matched analysis, the mean PSA values were significantly higher in the preDM group compared with the normoglycemia (NG) and T2DM groups (1.429 ng/mL vs. 1.086 ng/mL and 1.071 ng/mL; p < 0.05). In addition, multivariable linear regression analysis demonstrated that PSA was positively correlated with age, total cholesterol (TC) and preDM (p < 0.05). Negative correlation existed between PSA and T2DM (p < 0.05). Men with preDM had PSA values 31.6% higher than men without the condition (p < 0.05), whereas PSA levels were 17.5% lower in men with T2DM than in those without the condition (p < 0.05). CONCLUSIONS: Our results suggest preDM was an independent determinant of high PSA levels and support that men with T2DM had decreased PSA levels. Further larger studies are needed.


Subject(s)
Diabetes Mellitus, Type 2/blood , Kallikreins/blood , Prediabetic State/blood , Prostate-Specific Antigen/blood , Aged , Biomarkers/blood , Case-Control Studies , Cross-Sectional Studies , Humans , Male , Middle Aged
4.
Curr Med Res Opin ; 30(3): 423-30, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24156655

ABSTRACT

OBJECTIVE: An increasing number of studies show that exogenous insulin therapy may promote colorectal carcinogenesis. However, the results of the association between insulin therapy and risk of colorectal cancer (CRC) among type 2 diabetes patients are inconsistent. The purpose of our study is to examine the effect of insulin therapy on CRC risk among patients with type 2 diabetes in an updated meta-analysis. RESEARCH DESIGN AND METHODS: Medline and Embase were searched for the reference lists of pertinent articles published from January 1970 to April 2013. Two investigators independently extracted the data and reached consensus on the inclusion and exclusion criteria. Pooled relative risks and 95% confidence intervals were calculated with a random-effects model. RESULTS: Analysis of six studies, including 374,950 participants, showed that compared with non-insulin or metformin treatment, insulin treatment was associated with an increase of 37% in the risk of colorectal neoplasm among patients with type 2 diabetes, with moderate heterogeneity (I2=40%). The sensitivity analysis showed that exclusion of one small case-control study had no appreciable changes on the pooled results. Subgroup analyses suggested that there were significant positive associations between insulin therapy and risk of CRC in some subgroups, rather than all subgroups. CONCLUSIONS: Our meta-analysis supports a relationship between insulin therapy and increased risk of CRC in patients with type 2 diabetes. Because of bias and confounding of included studies, caution is needed when interpreting our results. Further investigations are needed.


Subject(s)
Colorectal Neoplasms/epidemiology , Insulin/therapeutic use , Humans , Risk Factors
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