Abstract

IntroductionThe NF-κB transcription factor family regulates several genes encoding pro-inflammatory and anti-inflammatory proteins in adipose tissues and in atherosclerotic plaques. The deletion variant allele of the NFKB1 - 94ins/delATTG promoter polymorphism leads to lower transcript levels of the p50 subunit, and the variant allele has been associated with the risk of several inflammatory diseases as well as coronary heart disease where inflammation is important in the pathogenesis. The objective of this study was to explore the potential interaction between the NFKB1-94ins/delATTG promoter polymorphism and general, abdominal, and gluteofemoral obesity in relation to the risk of incident acute coronary syndrome (ACS) in three large independent cohorts.Methods and ResultsThe analyses were conducted in the Danish prospective study Diet, Cancer and Health and the two US based cohorts; Nurses’ Health Study and Health Professionals Follow-up Study. We conducted sex stratified analyses that included 1202 male and 708 female cases of incident ACS. We observed a positive association for general and abdominal obesity with risk of incident ACS, independent of genotype in both genders. Gluteofemoral obesity was negatively associated with ACS risk in women independent of genotype, whereas there was no clear association for men. We calculated the relative excess risk due to interaction (RERI) and observed a statistically significant excess risk among men jointly exposed to general or abdominal obesity and the variant allele of the NFKB1-94ATTG polymorphism, whereas there was a tendency towards sub-additivity for gluteofemoral obesity. The excess risks in all analyses were, however, small and could not clearly be demonstrated in women.ConclusionThe variant allele of the NFKB1-94ins/delATTG promoter polymorphism did not substantially modify the association between obesity and incident ACS.

Highlights

  • The NF-kB transcription factor family regulates several genes encoding pro-inflammatory and antiinflammatory proteins in adipose tissues and in atherosclerotic plaques

  • Few were current smokers in Health Professionals Follow-up Study (HPFS) compared to Nurses’ Health Study (NHS) and DCH, and there were higher prevalence’s of hypertension, hypercholesterolemia and diabetes mellitus in the two US cohorts

  • We explored the possible interaction between obesity and carrier status by calculating the relative excess risk due to interaction (RERI) (Table S1)

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Summary

Introduction

The NF-kB transcription factor family regulates several genes encoding pro-inflammatory and antiinflammatory proteins in adipose tissues and in atherosclerotic plaques. The deletion variant allele of the NFKB1 - 94ins/ delATTG promoter polymorphism leads to lower transcript levels of the p50 subunit, and the variant allele has been associated with the risk of several inflammatory diseases as well as coronary heart disease where inflammation is important in the pathogenesis. The objective of this study was to explore the potential interaction between the NFKB1-94ins/delATTG promoter polymorphism and general, abdominal, and gluteofemoral obesity in relation to the risk of incident acute coronary syndrome (ACS) in three large independent cohorts. Many genes encoding pro-inflammatory and some genes encoding anti-inflammatory proteins in both adipose tissues and atherosclerotic plaques are regulated by the NF-kB transcription factor family[6,9,10,11]. The p50/p50 homodimer represses transcription of pro-inflammatory cytokines like TNFalpha and IL-12 and promotes transcription of the anti-inflammatory IL-10 [10,11]

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