Genomewide association study on monoclonal gammopathy of unknown significance (MGUS)

• Verfasst von: Thomsen, Hauke [VerfasserIn]
• Verfasst von: Weinhold, Niels [VerfasserIn]
• Verfasst von: Goldschmidt, Hartmut [VerfasserIn]
• Verfasst von: Hemminki, Kari [VerfasserIn]
• Verfasst von: Försti, Asta [VerfasserIn]
• Titel: Genomewide association study on monoclonal gammopathy of unknown significance (MGUS)
• Verf.angabe: Hauke Thomsen, Chiara Campo, Niels Weinhold, Miguel Inacio da Silva Filho, Luděk Pour, Evžen Gregora, Pavel Vodicka, Ludmila Vodickova, Per Hoffmann, Markus M. Nöthen, Karl-Heinz Jöckel, Christian Langer, Roman Hajek, Hartmut Goldschmidt, Kari Hemminki, Asta Försti
• E-Jahr: 2017
• Jahr: 04 April 2017
• Umfang: 10 S.
• Fussnoten: Gesehen am 09.05.2018
• Titel Quelle: Enthalten in: European journal of haematology
• Ort Quelle: Oxford : Wiley-Blackwell, 1987
• Jahr Quelle: 2017
• Band/Heft Quelle: 99(2017), 1, Seite 70-79
• ISSN Quelle: 1600-0609
• DOI: doi:10.1111/ejh.12892
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: germ line
• Sach-SW: low-risk genes
• Sach-SW: myeloma
• Sach-SW: susceptibility
• K10plus-PPN: 1574329146

Abstract

Objectives: To identify germ line variants contributing to the development of monoclonal gammopathy of undetermined significance (MGUS), an asymptomatic premalignant precursor for multiple myeloma (MM). Methods: We conducted the first genomewide association study (GWAS) on MGUS on 243 German cases with a replication on 294 Czech cases. Identified loci were further analyzed in 1508 German MM patients. New MM loci recently reported in a meta-analysis were also tested in the MGUS GWAS. Results: In GWAS, we identified 10 loci contributing to development of MGUS at P-value threshold of 10−5. The Czech cohort gave support for two associations (6q26, rs6933936; 7p21.3 rs10251201). In GWAS, rs974120 (8p23.2) reached genomewide significance (P=2.94×10−9), with a nominal significance in MM. The locus of rs974120 shows marks of transcriptional activity in leukemia according to ENCODE data. rs10251201 (7p21.3), rs9318227 (13q22.1), and rs10405859 (19q13.32) were associated with markers related to leukemogenesis and immune and inflammatory responses. Two newly identified candidate loci for MM, rs1948915 (8q24.21) and rs8058578 (16p11.2), were nominally associated with MGUS. Conclusions: These data allow a cautious first proposal for a germ line architecture of MGUS with links to leukemia and autoimmune conditions, the latter agreeing with a family study showing clustering of MGUS with autoimmune diseases.