County-level variation in the long-term association between PM2.5 and lung cancer mortality in China

2020 ◽  
Vol 738 ◽  
pp. 140195 ◽  
Author(s):  
Ning Wang ◽  
Kerrie Mengersen ◽  
Shilu Tong ◽  
Michael Kimlin ◽  
Maigeng Zhou ◽  
...  
Epidemiology ◽  
2005 ◽  
Vol 16 (5) ◽  
pp. S79 ◽  
Author(s):  
C Yap ◽  
I Beverland ◽  
R M. Agius ◽  
C Robertson ◽  
D J. Hole ◽  
...  

2011 ◽  
Vol 2011 (1) ◽  
Author(s):  
G. Thurston ◽  
R.T. Burnett ◽  
D. Krewski ◽  
M. Turner ◽  
Y. Shi ◽  
...  

2011 ◽  
Vol 2011 ◽  
pp. 1-4 ◽  
Author(s):  
Poul Suadicani ◽  
Hans Ole Hein ◽  
Finn Gyntelberg

Inflammation and genetic susceptibility influence the risk of lung cancer. During recent years, the role of complement as a part of the humoral response has advanced from being considered complementary to being regarded as a central element in innate immunity. C3 complement allotypes F and S have been associated with a number of inflammatory diseases. The C3F allele frequency is approximately 20% in Caucasian populations and the C3S approximately 80%, resulting in the three predominant genotypes FF (4%), FS (32%), and SS (64%). To our knowledge, no studies have investigated if different C3 allotypes or genotypes predict the risk of lung cancer. We tested in a long-term followup of 3,197 men aged 53 to 74 years the hypothesis that risk of lung cancer would depend on C3 complement genotypes. During 16 years, 160 subjects (5.0%) died from lung cancer, 68 men (6.1%) among complement C3 genotypes FS/FF, and 92 men (4.4%) among genotype SS; age-adjusted hazard ratio with 95%CI (HR) was 1.42 (1.04–1.94) and strongest, 2.71 (1.34–5.45), among the oldest fifth. C3 complement genotype variants were significantly associated with lung cancer mortality.


2016 ◽  
pp. ckw203 ◽  
Author(s):  
Raffaella Uccelli ◽  
Marina Mastrantonio ◽  
Pierluigi Altavista ◽  
Emanuela Caiaffa ◽  
Giorgio Cattani ◽  
...  

2020 ◽  
Vol 2020 (1) ◽  
Author(s):  
N. Wang ◽  
K. Mengersen ◽  
S. Tong ◽  
M. Kimlin ◽  
M. Zhou ◽  
...  

Author(s):  
Hong-Bae Kim ◽  
Jae-Yong Shim ◽  
Byoungjin Park ◽  
Yong-Jae Lee

The aim of this study was to examine the relationship between main air pollutants and all cancer mortality by performing a meta-analysis. We searched PubMed, EMBASE (a biomedical and pharmacological bibliographic database of published literature produced by Elsevier), and the reference lists of other reviews until April 2018. A random-effects model was employed to analyze the meta-estimates of each pollutant. A total of 30 cohort studies were included in the final analysis. Overall risk estimates of cancer mortality for 10 µg/m3 per increase of particulate matter (PM)2.5, PM10, and NO2 were 1.17 (95% confidence interval (CI): 1.11–1.24), 1.09 (95% CI: 1.04–1.14), and 1.06 (95% CI: 1.02–1.10), respectively. With respect to the type of cancer, significant hazardous influences of PM2.5 were noticed for lung cancer mortality and non-lung cancer mortality including liver cancer, colorectal cancer, bladder cancer, and kidney cancer, respectively, while PM10 had harmful effects on mortality from lung cancer, pancreas cancer, and larynx cancer. Our meta-analysis of cohort studies indicates that exposure to the main air pollutants is associated with increased mortality from all cancers.


2016 ◽  
Vol 571 ◽  
pp. 855-861 ◽  
Author(s):  
Xi Chen ◽  
Li-wen Zhang ◽  
Jia-ju Huang ◽  
Feng-ju Song ◽  
Luo-ping Zhang ◽  
...  

2020 ◽  
Vol 6 (Supplement_1) ◽  
pp. 23-23
Author(s):  
Zheng Su ◽  
Meng-Na Wei ◽  
Ya-Guang Fan ◽  
Zhi-Wei Hu ◽  
Jian-Ning Wang ◽  
...  

PURPOSE There is no long-term, population-based cohort screening evidence for lung cancer in China. This study aimed to evaluate whether increased screening rounds could reduce mortality as a result of lung cancer. METHODS We conducted a one-armed, prospective lung cancer screening cohort study with chest radiography and sputum cytology in Yunnan, People’s Republic of China, from 1992 to 1999. A total of 9,295 tin miners age 40 years or older were enrolled in this study and follow up ended on December 31, 2018. We stratified patients into 4 subgroups on the basis of screening rounds—1-2, 3-4, 5-6, or 7-8 rounds within 8 years—and selected 1-2 screening rounds within 8 years as the control group. Hazard ratios (HRs) and 95% CIs for the effect of screening rounds on mortality were estimated using Cox proportional hazards regression models. RESULTS Of participants, 831 (8.9%) were lost to follow up, and 4,517 patients died, 1,600 from cancer (1,135 from lung cancer), 1,519 from circulatory system diseases, and 619 from respiratory diseases. Participants who received 7-8 screening rounds within 8 years had reduced lung cancer mortality by 46% (HR, 0.54; 95% CI, 0.46 to 0.63 in all age groups. For those who received 5-6 screening rounds within 8 years, the benefit of reduction was mostly observed in patients older than age 52 years (HR, 0.63; 95% CI, 0.52 to 0.77), and there was no effect among those age 52 years or younger (HR, 0.72; 95% CI, 0.48 to 1.07). In contrast, only for those patients age 52 years or younger did 3-4 screening rounds within 8 years decrease mortality from lung cancer (HR, 0.56; 95% CI, 0.36 to 0.87). CONCLUSION We showed that increased screening rounds could reduce lung cancer mortality in a high-risk population, but the effect is influenced by age group. The optimal screening strategy for different age groups needs additional investigation.


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