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  • Courtney, Regina  (3)
  • Yoon, Hyung-Suk  (3)
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  • 1
    In: Carcinogenesis, Oxford University Press (OUP), Vol. 43, No. 6 ( 2022-06-27), p. 538-546
    Abstract: Helicobacter pylori infection has been suggested to be associated with lung cancer risk. However, information is lacking on whether the association differs by H. pylori antigen. We conducted a nested case-control study within the Southern Community Cohort Study, including 295 incident lung cancer cases and 295 controls. Helicobacter pylori multiplex serology assay was performed to detect antibodies to 15 H. pylori proteins. Conditional logistic regression was used to estimate odds ratios (ORs) and confidence intervals (95% CIs) after adjustment for covariates. Overall H. pylori+ was associated with a non-statistically significant increased risk of lung cancer (OR: 1.29; 95% CI: 0.85–1.95). Significant associations, however, were observed for H. pylori+ VacA+ (OR: 1.64; 95% CI: 1.02–2.62) and H. pylori+ Catalase+ (OR: 1.75; 95% CI: 1.11–2.77). The positive association of H. pylori+ Catalase+ with lung cancer risk was predominantly seen among African Americans (OR: 2.09; 95% CI: 1.11–3.95) but not European Americans (OR: 1.20; 95% CI: 0.56–2.54). Among participants who smoked ≥ 30 pack-years, overall H. pylori+ (OR: 1.85; 95% CI: 1.02–3.35), H. pylori+ CagA+ (OR: 2.77; 95% CI: 1.35–5.70), H. pylori+ VacA+ (OR: 2.53; 95% CI: 1.25–5.13) and H. pylori+ HP1564+ (OR: 2.01; 95% CI: 1.07–3.77) were associated with increased risk of lung cancer. Our study provides novel evidence that associations of H. pylori infection with lung cancer risk differ by H. pylori biomarker, may be more evident among African Americans and may be modified by smoking habits. Furthermore, studies are warranted to confirm our findings.
    Type of Medium: Online Resource
    ISSN: 0143-3334 , 1460-2180
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2022
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  • 2
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2023
    In:  Cancer Research Vol. 83, No. 7_Supplement ( 2023-04-04), p. 4201-4201
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 83, No. 7_Supplement ( 2023-04-04), p. 4201-4201
    Abstract: Introduction: Lung cancer is the leading cause of cancer death in the United States (U.S.). Lung cancer disproportionately affects African Americans (AAs) more than other racial/ethnic groups. Previous studies have linked liver diseases to lung cancer risk; however, few studies have evaluated the associations of circulating liver enzyme levels with lung cancer risk. In this study, we evaluated the associations of the serum alanine transaminase (ALT) and alkaline phosphatase (ALP) levels with the risk of subsequently developing lung cancer. Methods: We conducted a nested case-control study within the Southern Community Cohort Study, a well-conducted prospective cohort study in the southern U.S. mainly consisting of low-income AAs and European Americans (EAs). We included 552 incident lung cancer cases and 1,039 controls individually matched on age, sex, recruitment sites, and date of blood draw. Baseline serum levels of ALT and ALP were measured using the Beckman Coulter clinical chemistry analyzer. Conditional logistic regression and generalized estimating models were used to estimate odds ratios (ORs) and 95% confidence intervals (CIs) after adjusting for age, education, household income, body mass index (BMI), smoking status, pack-years, alcohol consumption, physical activity levels, history of chronic obstructive pulmonary disease, hypertension, and diabetes. Results: Higher serum levels of ALT were associated with a lower overall risk of lung cancer. Compared with the lowest tertile, participants in the second and third tertiles had OR (95% CI) of 0.74 (0.48-1.14) and 0.47 (0.28-0.78) (Ptrend & lt; 0.01). The inverse association was observed in both AAs and EAs. However, the inverse associations between serum ALT levels and lung cancer risk were more evident among men [ORT3 vs T1 = 0.36 (0.18-0.70)], current smokers [ORT3 vs T1 =0.65 (0.47-0.90)] , participants with lower BMI [ORT3 vs T1=0.55 (0.38-0.79)], or lower physical activity [ORT3 vs T1 = 0.55 (0.37-0.83)] . Stratified analyses by time interval between blood collection and lung cancer diagnosis showed that the inverse associations were observed in both those diagnosed within [ORT3 vs T1 =0.48 (0.23-1.00)] and after [ORT3 vs T1 = 0.36 (0.19-0.69)] a median follow up time of 3 years. The serum ALT level was not associated with overall lung cancer; however, higher serum ALP levels were significantly associated with increased lung cancer risk among AA men [ORT3 vs T1 = 1.98 (1.18-3.34)]. Conclusion: Our results indicate that in a predominantly low-income AA and EA population, serum ALT levels may be related to a lower risk of lung cancer. Further studies are warranted to confirm our findings and elucidate the potential underlying mechanisms of the associations. Citation Format: Shuai Xu, Hui Cai, Jie Wu, Hyung-Suk Yoon, Regina Courtney, Xiao-Ou Shu, William J. Blot, Wei Zheng, Qiuyin Cai. Associations of pre-diagnostic serum liver enzymes levels with lung cancer risk: results from the Southern Community Cohort Study. [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2023; Part 1 (Regular and Invited Abstracts); 2023 Apr 14-19; Orlando, FL. Philadelphia (PA): AACR; Cancer Res 2023;83(7_Suppl):Abstract nr 4201.
    Type of Medium: Online Resource
    ISSN: 1538-7445
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2023
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  • 3
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 80, No. 16_Supplement ( 2020-08-15), p. 1052-1052
    Abstract: Lung cancer is the leading cause of cancer death in the United States and many other countries. Helicobacter pylori (H. pylori), a Group 1 carcinogen classified by IARC, is a common bacteria infecting humans. Emerging evidence supports a possible etiological role of H. pylori infection in lung cancer. H. pylori has evolved over time to become highly genetically diverse, with substantial variations in the presence or levels of virulence factors. To evaluate the associations of lung cancer risk with H. pylori seropositivity, overall and by antigen-specific biomarkers, we conducted a nested case-control study using resources from the Southern Community Cohort Study (SCCS) including ~86,000 participants, two-thirds of whom are African American. A total of 295 incident lung cancer cases and 295 matched controls were included in this study. Controls were matched to cases on age, sex, race, recruitment site and date of blood draw. H. pylori multiplex serology assay was performed to detect levels of IgA, IgM and IgG antibodies to 15 H. pylori proteins. Overall H. pylori seropositivity (H. pylori+) was defined as being positive to any 4 or more H. pylori antigens. Individual H. pylori antigens were considered as seropositive only when the sample was simultaneously considered overall H. pylori+, which ensured that antigen-specific seropositivity was not based on cross-reactive antibody responses from infection with other pathogens expressing homologous proteins. Multivariable logistic regression models were used to estimate odds ratios (ORs) and corresponding confidence intervals (95% CIs) for lung cancer risk associated with seropositivity of H. pylori after adjusting for age, smoking status, pack-years, alcohol consumption, education, household income, BMI and history of COPD. Overall H. pylori+ was associated with a non-statistically significant increased lung cancer risk (OR, 1.29; 95% CI, 0.85-1.95). Associations were stronger for H. pylori+ VacA+ (OR, 1.64; 95% CI, 1.02-2.62) and H. pylori+ Catalase+ (OR, 1.75; 95% CI, 1.11-2.77), the latter more so among African Americans (OR, 2.09; 95% CI, 1.11-3.95) than European Americans (OR, 1.20; 95% CI, 0.56-2.54). Among people who smoked ≥ 30 pack-years, overall H. pylori+ (OR, 1.85; 95% CI, 1.02-3.35), H. pylori+ CagA+ (OR, 2.77; 95% CI, 1.35-5.70), H. pylori+ VacA+ (OR, 2.53; 95% CI, 1.25-5.13) and H. pylori+ Omp+ (OR, 2.01; 95% CI, 1.07-3.77) were associated with increased lung cancer risk. Among current and former smokers, significant interactions were observed for H. pylori+ CagA+ (p for interaction = 0.01) and H. pylori+ VacA+ (p for interaction = 0.03) between those who smoked ≥ 30 pack-years and those who smoked & lt; 30 pack-years. In summary, our results indicate that H. pylori infection may be associated with an elevated risk of lung cancer, and the associated risk might differ by antigen-specific H. pylori biomarkers and smoking amount. Further studies are warranted to confirm our findings. Citation Format: Hyung-Suk Yoon, Wei Zheng, Hui Cai, Jie Wu, Wanqing Wen, Regina Courtney, Angelika Michel, Michael Pawlita, Tim Waterboer, Qiuyin Cai. Associations of Helicobacter pylori biomarkers with lung cancer risk among low-income and African American populations: Results from the Southern Community Cohort Study [abstract] . In: Proceedings of the Annual Meeting of the American Association for Cancer Research 2020; 2020 Apr 27-28 and Jun 22-24. Philadelphia (PA): AACR; Cancer Res 2020;80(16 Suppl):Abstract nr 1052.
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
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    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2020
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    detail.hit.zdb_id: 410466-3
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