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1.
Sci Total Environ ; 885: 163869, 2023 Aug 10.
Artículo en Inglés | MEDLINE | ID: mdl-37142043

RESUMEN

There is little known about the global burden of CVD attributable to ambient PM2.5 (referred to as CVD burden hereinafter) and its secular trend across different regions and countries. We aimed to evaluate the spatiotemporal trends in CVD burden at the global, regional and national levels from 1990 to 2019. Data on CVD burden including mortality and disability adjusted of life years (DALYs) from 1990 to 2019 were extracted from the Global Burden of Disease Study 2019. Cases, the age-standardized rate of mortality (ASMR) and DALYs (ASDR) were estimated by age, sex and sociodemographic index (SDI). Estimated annual percentage change (EAPC) was calculated to evaluate the temporal changing in ASDR and ASMR from 1990 to 2019. In 2019, 2.48 million deaths and 60.91 million DALYs of CVD were attributed to ambient PM2.5 globally. Most CVD burden occurred in males, elderly and the middle SDI region. At national level, Uzbekistan, Egypt, and Iraq had the highest ASMR and ASDR. Despite remarkable increase in number of DALYs and deaths of CVD worldwide from 1990 to 2019, we observed nonsignificant change in ASMR (EAPC: 0.06, 95 % CI: -0.01, 0.13) and slight increment in ASDR (EAPC: 0.30, 95 % CI: 0.23, 0.37). The EAPCs of ASMR and ASDR were negatively associated with SDI in 2019, while the low-middle SDI region exhibited the fastest growth of ASMR and ASDR with EAPCs of 3.25 (95 % CI: 3.14, 3.37) and 3.36 (95 % CI: 3.22, 3.49), respectively. In conclusion, the global CVD burden attributable to ambient PM2.5 has largely increased over the past three decades. The population growth, aging and SDI contributed to the heterogeneity of spatial and temporal distribution. Enforcing policy to improving air quality is required to halt the growing burden of PM2.5 on health.


Asunto(s)
Enfermedades Cardiovasculares , Anciano , Masculino , Humanos , Enfermedades Cardiovasculares/epidemiología , Carga Global de Enfermedades , Percepción Social , Envejecimiento , Material Particulado , Años de Vida Ajustados por Calidad de Vida
2.
Biomed Environ Sci ; 35(10): 911-920, 2022 Oct 20.
Artículo en Inglés | MEDLINE | ID: mdl-36443268

RESUMEN

Objective: The purpose of this study was to determine the serum uric acid levels and the prevalence of hyperuricemia among Chinese adults in 2015 and compare the differences between urban and rural areas, as well as the differences between eastern, central, and western regions. Methods: A national representative sample of 180,208 participants were included using a stratified, multistage, and random sampling method. The demographic characteristics and blood samples were collected to determine the serum uric acid levels and prevalence of hyperuricemia among subgroups using complicated sampling weight. A t-test or ANOVA was used for normally-distributed data. The Kruskal-Wallis rank test was used for skewed-distributed data. The Mantel-Haenszel chi-square test was used to compare the difference in categorical variables. Results: The weighted mean uric acid level in Chinese adults was 310.4 µmol/L (317.5 µmol/L in urban areas and 302.9 µmol/L in rural areas). The weighted average values of uric acid in eastern, central, and western China were 315.5 µmol/L, 303.5 µmol/L, and 310.4 µmol/L, respectively. The weighted prevalence of hyperuricemia in Chinese adults was 14.6%, with a prevalence of 16.5% in urban areas and 12.5% in rural areas. The weighted prevalence of hyperuricemia in eastern, central, and western China was 16.0%, 12.5%, and 14.8%, respectively. Conclusion: The uric acid level in Chinese adults is relatively high. Effective actions are warranted to improve this metabolic abnormality.


Asunto(s)
Hiperuricemia , Adulto , Humanos , Hiperuricemia/epidemiología , Ácido Úrico , Estado Nutricional , Pueblo Asiatico , China/epidemiología
3.
Asia Pac J Clin Nutr ; 26(2): 271-277, 2017 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-28244705

RESUMEN

BACKGROUND AND OBJECTIVES: Several epidemiological studies investigating the association between dietary vitamin E intake and the risk of lung cancer have demonstrated inconsistent results. Hence, a meta-analysis was conducted to summarise evidence of the association of dietary vitamin E intake with the risk of lung cancer. METHODS AND STUDY DESIGN: In this meta-analysis, a systematic literature search of PubMed and Web of Science was conducted to identify relevant studies published from 1955 to April 2015. If p<0.05 or I2 >50%, a random effect model was used to estimate overall relative risks (RRs) and 95% confidence intervals (CIs). Otherwise, a fixed effect model was applied. Publication bias was estimated using the funnel plot and Egger's test. The doseresponse relationship was assessed using the method of restricted cubic splines with 4 knots at percentiles 5, 35, 65, and 95 of the distribution. RESULTS: The pooled RR of lung cancer for the highest versus lowest categories of dietary vitamin E intake was 0.84 (95% CI=0.76-0.93). With every 2 mg/d increase in dietary vitamin E intake, the risk of lung cancer statistically decreased by 5% (RR=0.95, 95% CI =0.91-0.99, plinearity=0.0237). CONCLUSIONS: Our analysis suggests that higher dietary vitamin E intake exerts a protective effect against lung cancer.


Asunto(s)
Dieta , Neoplasias Pulmonares/prevención & control , Vitamina E/administración & dosificación , Relación Dosis-Respuesta a Droga , Humanos , Neoplasias Pulmonares/epidemiología , Masculino , Riesgo
4.
World J Gastroenterol ; 22(5): 1911-8, 2016 Feb 07.
Artículo en Inglés | MEDLINE | ID: mdl-26855551

RESUMEN

AIM: To evaluate the relationship between glutathione S-transferase M1 (GSTM1) polymorphism and susceptibility to esophageal cancer (EC). METHODS: A comprehensive search of the United States National Library of Medicine PubMed database and the Elsevier, Springer, and China National Knowledge Infrastructure databases for all relevant studies was conducted using combinations of the following terms: "glutathione S-transferase M1", "GSTM1", "polymorphism", and "EC" (until November 1, 2014). The statistical analysis was performed using the SAS software (v.9.1.3; SAS Institute, Cary, NC, United States) and the Review Manager software (v.5.0; Oxford, England); crude odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the association between the GSTM1 null genotype and the risk of EC. RESULTS: A total of 37 studies involving 2236 EC cases and 3243 controls were included in this meta-analysis. We observed that the GSTM1 null genotype was a significant risk factor for EC in most populations (OR = 1.33, 95%CI: 1.12-1.57, P heterogeneity < 0.000001, and I (2) = 77.0%), particularly in the Asian population (OR = 1.53, 95%CI: 1.26-1.86, P heterogeneity < 0.000001, and I (2) = 77.0%), but not in the Caucasian population (OR = 1.02, 95%CI: 0.87-1.19, P heterogeneity = 0.97, and I (2) = 0%). CONCLUSION: The GSTM1 null polymorphism may be associated with an increased risk for EC in Asian but not Caucasian populations.


Asunto(s)
Neoplasias Esofágicas/genética , Glutatión Transferasa/genética , Polimorfismo Genético , Pueblo Asiatico/genética , Estudios de Casos y Controles , Distribución de Chi-Cuadrado , Neoplasias Esofágicas/diagnóstico , Neoplasias Esofágicas/enzimología , Neoplasias Esofágicas/epidemiología , Estudios de Asociación Genética , Predisposición Genética a la Enfermedad , Humanos , Oportunidad Relativa , Fenotipo , Medición de Riesgo , Factores de Riesgo
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