TY - JOUR
T1 - Distribution of RET mutations in multiple endocrine neoplasia 2 in Denmark 1994-2014
T2 - a nationwide study
AU - Mathiesen, Jes Sloth
AU - Kroustrup, Jens Peter
AU - Vestergaard, Peter
AU - Stochholm, Kirstine
AU - Poulsen, Per Løgstrup
AU - Rasmussen, Åse Krogh
AU - Feldt-Rasmussen, Ulla
AU - Gaustadnes, Mette
AU - Ørntoft, Torben Falck
AU - Hansen, Thomas V O
AU - Nielsen, Finn Cilius
AU - Brixen, Kim
AU - Godballe, Christian
AU - Frederiksen, Anja Lisbeth
PY - 2017
Y1 - 2017
N2 - Background Germline mutations of the REarranged during Transfection (RET) proto-oncogene cause multiple endocrine neoplasia 2 (MEN2). It is unclear whether the distribution of RET mutations varies among populations. We conducted the first nationwide study of the distribution of RET mutations and compared the results to those of other populations. Methods This retrospective cohort study included 1,583 patients, who underwent RET gene testing in one of three centers covering all of Denmark between September 1994 and December 2014. Primary testing method was Sanger sequencing, which included exons 8-11 and 13-16. Mutations were defined according to the ARUP database July 1st 2016. Results RET mutations were identified in 163 patients from 36 apparently unrelated families. Among the 36 families 13 (36.1%) carried mutations in codon 611, four (11.1%) in codon 618, three (8.3%) in codon 620, one (2.8%) in codon 631, six (16.7%) in codon 634, one (2.8%) in codon 790, one (2.8%) in codon 804, one (2.8%) in codon 852, one (2.8%) in codon 883 and five (13.9%) in codon 918. Among the 13 families with codon 611 mutations, 12 had the p.C611Y mutation. Conclusions The distribution of RET mutations in Denmark appears to differ from that of other populations. Mutations in codon 611 were the most prevalent followed by more frequently reported mutations. This might be due to a possible founder effect for the p.C611Y mutation. However, further studies are needed to find possible explanations for the skewed mutational spectrum in Denmark.
AB - Background Germline mutations of the REarranged during Transfection (RET) proto-oncogene cause multiple endocrine neoplasia 2 (MEN2). It is unclear whether the distribution of RET mutations varies among populations. We conducted the first nationwide study of the distribution of RET mutations and compared the results to those of other populations. Methods This retrospective cohort study included 1,583 patients, who underwent RET gene testing in one of three centers covering all of Denmark between September 1994 and December 2014. Primary testing method was Sanger sequencing, which included exons 8-11 and 13-16. Mutations were defined according to the ARUP database July 1st 2016. Results RET mutations were identified in 163 patients from 36 apparently unrelated families. Among the 36 families 13 (36.1%) carried mutations in codon 611, four (11.1%) in codon 618, three (8.3%) in codon 620, one (2.8%) in codon 631, six (16.7%) in codon 634, one (2.8%) in codon 790, one (2.8%) in codon 804, one (2.8%) in codon 852, one (2.8%) in codon 883 and five (13.9%) in codon 918. Among the 13 families with codon 611 mutations, 12 had the p.C611Y mutation. Conclusions The distribution of RET mutations in Denmark appears to differ from that of other populations. Mutations in codon 611 were the most prevalent followed by more frequently reported mutations. This might be due to a possible founder effect for the p.C611Y mutation. However, further studies are needed to find possible explanations for the skewed mutational spectrum in Denmark.
U2 - 10.1089/thy.2016.0411
DO - 10.1089/thy.2016.0411
M3 - Journal article
C2 - 27809725
SN - 1050-7256
VL - 27
SP - 215
EP - 223
JO - Thyroid
JF - Thyroid
IS - 2
ER -