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1.
Math Biosci Eng ; 17(4): 2842-2852, 2020 03 25.
Article in English | MEDLINE | ID: mdl-32987501

ABSTRACT

Since the first case of coronavirus disease (COVID-19) in Wuhan Hubei, China, was reported in December 2019, COVID-19 has spread rapidly across the country and overseas. The first case in Anhui, a province of China, was reported on January 10, 2020. In the field of infectious diseases, modeling, evaluating and predicting the rate of disease transmission is very important for epidemic prevention and control. Different intervention measures have been implemented starting from different time nodes in the country and Anhui, the epidemic may be divided into three stages for January 10 to February 11, 2020, namely. We adopted interrupted time series method and develop an SEI/QR model to analyse the data. Our results displayed that the lockdown of Wuhan implemented on January 23, 2020 reduced the contact rate of epidemic transmission in Anhui province by 48.37%, and centralized quarantine management policy for close contacts in Anhui reduced the contact rate by an additional 36.97%. At the same time, the estimated basic reproduction number gradually decreased from the initial 2.9764 to 0.8667 and then to 0.5725. We conclude that the Wuhan lockdown and the centralized quarantine management policy in Anhui played a crucial role in the timely and effective mitigation of the epidemic in Anhui. One merit of this work is the adoption of morbidity data which may reflect the epidemic more accurately and promptly. Our estimated parameters are largely in line with the World Health Organization estimates and previous studies.


Subject(s)
Betacoronavirus , Coronavirus Infections/epidemiology , Models, Biological , Pandemics , Pneumonia, Viral/epidemiology , Basic Reproduction Number/statistics & numerical data , COVID-19 , China/epidemiology , Computer Simulation , Coronavirus Infections/prevention & control , Coronavirus Infections/transmission , Humans , Interrupted Time Series Analysis/statistics & numerical data , Markov Chains , Mathematical Concepts , Monte Carlo Method , Morbidity/trends , Pandemics/prevention & control , Pandemics/statistics & numerical data , Pneumonia, Viral/prevention & control , Pneumonia, Viral/transmission , Quarantine/statistics & numerical data , SARS-CoV-2
2.
Respir Physiol Neurobiol ; 247: 12-19, 2018 01.
Article in English | MEDLINE | ID: mdl-28870868

ABSTRACT

The aim of the present study was to investigate whether heme oxygenase-1(HO-1) participated in the resolution of seawater drowning-induced acute respiratory distress syndrome (ARDS). In this study, gross and microscopic morphology of pulmonary tissue, computed tomography images and biochemical indexes were continuously observed from 15min to 15day after seawater drowning. The content and activity of HO-1 were determined by western-blot and spectrophotometric method, respectively. The morphological and biochemical indexes indicated that the seawater drowning could lead to the serious pulmonary hemorrhage and edema. However, 6h after drowning, these morphological and biochemical indexes gradually returned to basal level. Meanwhile, seawater drowning increased the HO-1 expression and activity while Zinc protoporphyrin (a HO-1 specific activity inhibitor) decreased the content of transforming growth factor beta-1 in lung tissue and hampered the repair process of seawater drowning-induced ARDS. Thus, HO-1 participates in the resolution of seawater drowning-induced ARDS.


Subject(s)
Drowning/enzymology , Heme Oxygenase-1/metabolism , Membrane Proteins/metabolism , Respiratory Distress Syndrome/enzymology , Respiratory Distress Syndrome/etiology , Seawater , Animals , Disease Models, Animal , Disease Progression , Drowning/diagnostic imaging , Drowning/pathology , Edema/diagnostic imaging , Edema/enzymology , Edema/etiology , Edema/pathology , Enzyme Inhibitors/pharmacology , Heme Oxygenase-1/antagonists & inhibitors , Hemorrhage/diagnostic imaging , Hemorrhage/enzymology , Hemorrhage/etiology , Hemorrhage/pathology , Lung/diagnostic imaging , Lung/drug effects , Lung/enzymology , Lung/pathology , Male , Membrane Proteins/antagonists & inhibitors , Mice, Inbred ICR , Protoporphyrins/pharmacology , Random Allocation , Recovery of Function/physiology , Respiratory Distress Syndrome/diagnostic imaging , Respiratory Distress Syndrome/pathology
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