| Literature DB >> 23647020 |
Alexandra J Greenberg1,2, Margot Cousin2, Shaji Kumar3, Rhett P Ketterling4, Ryan A Knudson4, Dirk Larson5, Colin Colby5, Christopher Scott5, Celine M Vachon1, S Vincent Rajkumar3.
Abstract
We previously reported an increased risk of monoclonal gammopathy of undetermined significance (MGUS) in first-degree relatives of MGUS and multiple myeloma patients. Here, we examine whether primary cytogenetic categories of myeloma differ between patients with and without a family history of MGUS or myeloma. We studied 201 myeloma patients with available data on family history and molecular cytogenetic classification. Myeloma with trisomies was more common in probands who had an affected first-degree relative with MGUS or myeloma compared with those without a family history (46.9% vs. 33.5%, P = 0.125); however, the difference was not statistically significant. Additional studies on the cytogenetic types of myeloma associated with familial tendency are needed.Entities:
Keywords: cytogenetics; family history; monoclonal gammopathy of undetermined significance; multiple myeloma
Mesh:
Year: 2013 PMID: 23647020 PMCID: PMC3762589 DOI: 10.1111/ejh.12133
Source DB: PubMed Journal: Eur J Haematol ISSN: 0902-4441 Impact factor: 3.674