Interactions between inflammatory gene polymorphisms and HTLV-I infection for total death, incidence of cancer, and atherosclerosis-related diseases among the Japanese population
Background: An increased risk of total death owing to human T-lymphotropic virus type-I (HTLV-I) infection has been reported. However, its etiology and protective factors are unclear. Various studies reported fluctuations in immune-inflammatory status among HTLV-I carriers. We conducted a matched co...
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Format: | Article |
Language: | English |
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Japan Epidemiological Association
2017-09-01
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Series: | Journal of Epidemiology |
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Online Access: | https://www.jstage.jst.go.jp/article/jea/27/9/27_JE83/_pdf |
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author | Tara Sefanya Kairupan |
author_facet | Tara Sefanya Kairupan |
author_sort | Tara Sefanya Kairupan |
collection | DOAJ |
description | Background: An increased risk of total death owing to human T-lymphotropic virus type-I (HTLV-I) infection has been reported. However, its etiology and protective factors are unclear. Various studies reported fluctuations in immune-inflammatory status among HTLV-I carriers. We conducted a matched cohort study among the general population in an HTLV-I-endemic region of Japan to investigate the interaction between inflammatory gene polymorphisms and HTLV-I infection for total death, incidence of cancer, and atherosclerosis-related diseases.
Method: We selected 2180 sub-cohort subjects aged 35–69 years from the cohort population, after matching for age, sex, and region with HTLV-I seropositives. They were followed up for a maximum of 10 years. Inflammatory gene polymorphisms were selected from TNF-α, IL-10, and NF-κB1. A Cox proportional hazard model was used to estimate the hazard ratio (HR) and the interaction between gene polymorphisms and HTLV-I for risk of total death and incidence of cancer and atherosclerosis-related diseases.
Results: HTLV-I seropositivity rate was 6.4% in the cohort population. The interaction between TNF-α 1031T/C and HTLV-I for atherosclerosis-related disease incidence was statistically significant (p = 0.020). No significant interaction was observed between IL-10 819T/C or NF-κB1 94ATTG ins/del and HTLV-I. An increased HR for total death was observed in the Amami island region, after adjustment of various factors with gene polymorphisms (HR 3.03; 95% confidence interval, 1.18–7.77).
Conclusion: The present study found the interaction between TNF-α 1031T/C and HTLV-I to be a risk factor for atherosclerosis-related disease. Further follow-up is warranted to investigate protective factors against developing diseases among susceptible HTLV-I carriers. |
first_indexed | 2024-04-13T05:37:31Z |
format | Article |
id | doaj.art-841671f9ad9242749f974d8622b50f4e |
institution | Directory Open Access Journal |
issn | 0917-5040 1349-9092 |
language | English |
last_indexed | 2024-04-13T05:37:31Z |
publishDate | 2017-09-01 |
publisher | Japan Epidemiological Association |
record_format | Article |
series | Journal of Epidemiology |
spelling | doaj.art-841671f9ad9242749f974d8622b50f4e2022-12-22T03:00:14ZengJapan Epidemiological AssociationJournal of Epidemiology0917-50401349-90922017-09-0127942042710.1016/j.je.2016.08.017Interactions between inflammatory gene polymorphisms and HTLV-I infection for total death, incidence of cancer, and atherosclerosis-related diseases among the Japanese populationTara Sefanya KairupanBackground: An increased risk of total death owing to human T-lymphotropic virus type-I (HTLV-I) infection has been reported. However, its etiology and protective factors are unclear. Various studies reported fluctuations in immune-inflammatory status among HTLV-I carriers. We conducted a matched cohort study among the general population in an HTLV-I-endemic region of Japan to investigate the interaction between inflammatory gene polymorphisms and HTLV-I infection for total death, incidence of cancer, and atherosclerosis-related diseases. Method: We selected 2180 sub-cohort subjects aged 35–69 years from the cohort population, after matching for age, sex, and region with HTLV-I seropositives. They were followed up for a maximum of 10 years. Inflammatory gene polymorphisms were selected from TNF-α, IL-10, and NF-κB1. A Cox proportional hazard model was used to estimate the hazard ratio (HR) and the interaction between gene polymorphisms and HTLV-I for risk of total death and incidence of cancer and atherosclerosis-related diseases. Results: HTLV-I seropositivity rate was 6.4% in the cohort population. The interaction between TNF-α 1031T/C and HTLV-I for atherosclerosis-related disease incidence was statistically significant (p = 0.020). No significant interaction was observed between IL-10 819T/C or NF-κB1 94ATTG ins/del and HTLV-I. An increased HR for total death was observed in the Amami island region, after adjustment of various factors with gene polymorphisms (HR 3.03; 95% confidence interval, 1.18–7.77). Conclusion: The present study found the interaction between TNF-α 1031T/C and HTLV-I to be a risk factor for atherosclerosis-related disease. Further follow-up is warranted to investigate protective factors against developing diseases among susceptible HTLV-I carriers.https://www.jstage.jst.go.jp/article/jea/27/9/27_JE83/_pdfHTLV-IGene polymorphismInflammationInteraction |
spellingShingle | Tara Sefanya Kairupan Interactions between inflammatory gene polymorphisms and HTLV-I infection for total death, incidence of cancer, and atherosclerosis-related diseases among the Japanese population Journal of Epidemiology HTLV-I Gene polymorphism Inflammation Interaction |
title | Interactions between inflammatory gene polymorphisms and HTLV-I infection for total death, incidence of cancer, and atherosclerosis-related diseases among the Japanese population |
title_full | Interactions between inflammatory gene polymorphisms and HTLV-I infection for total death, incidence of cancer, and atherosclerosis-related diseases among the Japanese population |
title_fullStr | Interactions between inflammatory gene polymorphisms and HTLV-I infection for total death, incidence of cancer, and atherosclerosis-related diseases among the Japanese population |
title_full_unstemmed | Interactions between inflammatory gene polymorphisms and HTLV-I infection for total death, incidence of cancer, and atherosclerosis-related diseases among the Japanese population |
title_short | Interactions between inflammatory gene polymorphisms and HTLV-I infection for total death, incidence of cancer, and atherosclerosis-related diseases among the Japanese population |
title_sort | interactions between inflammatory gene polymorphisms and htlv i infection for total death incidence of cancer and atherosclerosis related diseases among the japanese population |
topic | HTLV-I Gene polymorphism Inflammation Interaction |
url | https://www.jstage.jst.go.jp/article/jea/27/9/27_JE83/_pdf |
work_keys_str_mv | AT tarasefanyakairupan interactionsbetweeninflammatorygenepolymorphismsandhtlviinfectionfortotaldeathincidenceofcancerandatherosclerosisrelateddiseasesamongthejapanesepopulation |