Pro-inflammatory genetic background and zinc status in old atheroscleroticsubjects.

Carmela Rita Balistreri, Calogero Caruso, Domenico Lio, Letizia Scola, Giuseppina Candore, Marco Malavolta, Elisa Muti, Robertina Giacconi, Eugenio Mocchegiani, Robertina Giacconi

Risultato della ricerca: Articlepeer review

25 Citazioni (Scopus)


Inflammation and genetics are prominent mechanisms in the pathogenesis of atherosclerosis (AT) and its complications. In this review we discuss the possible impact on AT development of several genetic determinants involved in inflammation, oxidative stress and cytoprotection (IL-6, TNF-alpha, IL-10, CD14, TLR4, MT, HSP70). Genetic polymorphisms of these genes may affect a differential inflammatory response predisposing to AT. However, allelic polymorphisms of genes which increase the risk of AT frequently occur in the general population but, only adequate gene-environment-polymorphism interactions promote the onset of the disease. Zinc deficiency has been suggested as an environmental risk factor for AT. With advancing age, the incidence of zinc deficiency increases for several reasons. Among them, dietary intake, malabsorption and genetic background of inflammatory markers may be involved. A crucial contribution may also be played by increased oxidative stress which may lead to the appearance of dysfunctional proteins, including metallothioneins (MT) that are in turn involved in zinc homeostasis. The detection of candidate genes related to inflammation and promoting AT and their reciprocal influence/interaction with zinc status might allow earlier appropriate dietary interventions in genetically susceptible subjects.
Lingua originaleEnglish
pagine (da-a)306-318
Numero di pagine13
RivistaAgeing Research Reviews
Stato di pubblicazionePublished - 2008

All Science Journal Classification (ASJC) codes

  • ???subjectarea.asjc.1300.1305???
  • ???subjectarea.asjc.1300.1303???
  • ???subjectarea.asjc.1300.1302???
  • ???subjectarea.asjc.1300.1312???
  • ???subjectarea.asjc.2800.2808???


Entra nei temi di ricerca di 'Pro-inflammatory genetic background and zinc status in old atheroscleroticsubjects.'. Insieme formano una fingerprint unica.

Cita questo