Association study of a new polymorphism in the PECAM-1 gene in multiple sclerosis

Francesca L. Sciacca, Cinzia Ferri, Sandra D'Alfonso, Elisabetta Bolognesi, Filippo Martinelli Boneschi, Barbara Cuzzilla, Bruno Colombo, Giancarlo Comi, Nicola Canal, Luigi M.E. Grimaldi

Risultato della ricerca: Contributo su rivistaArticolo in rivistapeer review

Abstract

Genetic polymorphisms of immunorelevant genes may modulate occurrence or clinical features of multifactorial diseases. PECAM-1 is an adhesion molecule crucial for transmigration of cells from blood to tissues, but its genetic contribution to multifactorial diseases has never been investigated. We have identified and characterized a tetranucleotide repeat polymorphism within the third intron of PECAM-1. In a cohort of healthy controls (HC), we found 10 alleles. An assessment of the association of this polymorphism with multiple sclerosis (MS) showed similar allele and genotype frequencies in HC and MS patients as well as in MS patients differing for the gravity of their disease course. We conclude that although potentially able to affect organ-specific autoimmune diseases, this new PECAM-1 polymorphism, does not seem to contribute to the genetic background of MS. Copyright (C) 2000 Elsevier Science B.V.

Lingua originaleInglese
pagine (da-a)174-178
Numero di pagine5
RivistaJournal of Neuroimmunology
Volume104
Numero di pubblicazione2
DOI
Stato di pubblicazionePubblicato - 1 mag 2000

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