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1.
Sci Total Environ ; 929: 172638, 2024 Jun 15.
Artículo en Inglés | MEDLINE | ID: mdl-38643869

RESUMEN

BACKGROUND: Although both air pollution and aging are related to the development of liver cirrhosis, the role of biological aging in association of the mixture of fine particulate matter (PM2.5) and its constituents with liver cirrhosis was unknown. METHODS: This case-control retrospective study included 100 liver cirrhosis patients and 100 control subjects matched by age and sex. The concentrations of PM2.5 and its constituents were estimated for patients using machine-learning methods. The clinical biomarkers were used to calculate biological age using the Klemera-Doubalmethod (KDM) algorithms. Individual associations of PM2.5 and its constituents or biological age with liver cirrhosis were analyzed by generalized linear models. WQS and BKMR were applied to analyze association of mixture of PM2.5 and its constituents with liver cirrhosis. The mediation effect of biological age on associations of PM2.5 and its constituents with liver cirrhosis was further explored. RESULTS: we found that each 1-unit increment in NH4+, NO3-, SO42- and biological age were related to 3.618-fold (95%CI: 1.896, 6.904), 1.880-fold (95%CI: 1.319, 2.680), 2.955-fold (95%CI: 1.656, 5.272) and 1.244-fold (95%CI: 1.093, 1.414) increased liver cirrhosis. Both WQS and BKMR models showed that the mixture of PM2.5 and its constituents was related to increased liver cirrhosis. Furthermore, the mediated proportion of biological age on associations of NH4+ and SO42- with liver cirrhosis were 14.7 % and 14.6 %, respectively. CONCLUSIONS: Biological aging may partly explain the exposure to PM2.5 and its constituents in association with increased risk for liver cirrhosis, implying that delaying the aging process may be a key step for preventing PM2.5-related liver cirrhosis risk.


Asunto(s)
Contaminantes Atmosféricos , Cirrosis Hepática , Material Particulado , Sulfatos , Humanos , Material Particulado/análisis , Contaminantes Atmosféricos/análisis , Femenino , Masculino , Estudios de Casos y Controles , Persona de Mediana Edad , Sulfatos/análisis , Compuestos de Amonio , Estudios Retrospectivos , Contaminación del Aire/estadística & datos numéricos , Exposición a Riesgos Ambientales/estadística & datos numéricos , Anciano , Envejecimiento
2.
Transl Psychiatry ; 12(1): 173, 2022 04 28.
Artículo en Inglés | MEDLINE | ID: mdl-35484098

RESUMEN

Risperidone is routinely used in the clinical management of schizophrenia, but the treatment response is highly variable among different patients. The genetic underpinnings of the treatment response are not well understood. We performed a pharmacogenomic study of the treatment response to risperidone in patients with schizophrenia by using a SNP microarray -based genome-wide association study (GWAS) and whole exome sequencing (WES)-based GWAS. DNA samples were collected from 189 patients for the GWAS and from 222 patients for the WES after quality control in multiple centers of China. Antipsychotic response phenotypes of patients who received eight weeks of risperidone treatment were quantified with percentage change on the Positive and Negative Syndrome Scale (PANSS). The GWAS revealed a significant association between several SNPs and treatment response, such as three GRM7 SNPs (rs141134664, rs57521140, and rs73809055). Gene-based analysis in WES revealed 13 genes that were associated with antipsychotic response, such as GPR12 and MAP2K3. We did not identify shared loci or genes between GWAS and WES, but association signals tended to cluster into the GPCR gene family and GPCR signaling pathway, which may play an important role in the treatment response etiology. This study may provide a research paradigm for pharmacogenomic research, and these data provide a promising illustration of our potential to identify genetic variants underlying antipsychotic responses and may ultimately facilitate precision medicine in schizophrenia.


Asunto(s)
Antipsicóticos , Esquizofrenia , Antipsicóticos/uso terapéutico , Estudio de Asociación del Genoma Completo , Humanos , Risperidona/uso terapéutico , Esquizofrenia/inducido químicamente , Esquizofrenia/tratamiento farmacológico , Esquizofrenia/genética , Secuenciación del Exoma
3.
Int J Biol Macromol ; 181: 778-785, 2021 Jun 30.
Artículo en Inglés | MEDLINE | ID: mdl-33798587

RESUMEN

A batch experiment was carried out in order to remove Hg2+ from the aqueous solution as well as the polluted water using modified chitosan (CS) with polyamine compounds (triethylenetetramine (TETA), tetraethylenepentamine (TEPA)), and melamine. The obtained polyamine-co-melamine crosslinked CS derivatives (MCS-4N and MCS-5N) were characterized and used as adsorbents. In comparison to the raw CS, the modification significantly promoted the adsorption of Hg2+ ions. The results of the pseudo-second-order kinetic model revealed that pH-dependent derivatives adsorbents achieved the equilibrium state within 12 h. The Langmuir model was best fitted with the Hg2+ adsorption isotherm and showed the highest adsorption capacities of 140.3 and 109.7 mg/g for MCS-4N and MCS-5N, respectively. A slight decrease in the adsorption efficiency of Hg2+ was noticed with the increment of the ionic strength of the solution. However, the studied adsorbents were easily regenerated and presented adequate reusability. The Hg2+ adsorption was regulated by the combined process of coordination reaction and electrostatic attraction as well. The as-prepared polyamine-co-melamine crosslinked CS derivatives were found potential adsorbents for the adsorptive capture of Hg2+ ions from aqueous solutions and polluted waters.


Asunto(s)
Quitosano/química , Reactivos de Enlaces Cruzados/química , Mercurio/aislamiento & purificación , Poliaminas/química , Triazinas/química , Contaminantes Químicos del Agua/aislamiento & purificación , Purificación del Agua , Adsorción , Concentración de Iones de Hidrógeno , Iones , Concentración Osmolar , Soluciones , Espectroscopía Infrarroja por Transformada de Fourier , Factores de Tiempo
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