TY - JOUR
T1 - The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice
AU - Forzano, F.
AU - Antonova, O.
AU - Clarke, A.
AU - de Wert, G.
AU - Hentze, S.
AU - Jamshidi, Y.
AU - Moreau, Y.
AU - Perola, M.
AU - Prokopenko, I.
AU - Read, A.
AU - Reymond, A.
AU - Stefansdottir, V.
AU - van El, C.
AU - Genuardi, M.
AU - Executive Committee of the European Society of Human Genetics
AU - Public and Professional Policy Committee of the European Society of Human Genetics
PY - 2022/5
Y1 - 2022/5
N2 - Y Polygenic risk score analyses on embryos (PGT-P) are being marketed by some private testing companies to parents using in vitro fertilisation as being useful in selecting the embryos that carry the least risk of disease in later life. It appears that at least one child has been born after such a procedure. But the utility of a PRS in this respect is severely limited, and to date, no clinical research has been performed to assess its diagnostic effectiveness in embryos. Patients need to be properly informed on the limitations of this use of PRSs, and a societal debate, focused on what would be considered acceptable with regard to the selection of individual traits, should take place before any further implementation of the technique in this population.
AB - Y Polygenic risk score analyses on embryos (PGT-P) are being marketed by some private testing companies to parents using in vitro fertilisation as being useful in selecting the embryos that carry the least risk of disease in later life. It appears that at least one child has been born after such a procedure. But the utility of a PRS in this respect is severely limited, and to date, no clinical research has been performed to assess its diagnostic effectiveness in embryos. Patients need to be properly informed on the limitations of this use of PRSs, and a societal debate, focused on what would be considered acceptable with regard to the selection of individual traits, should take place before any further implementation of the technique in this population.
U2 - 10.1038/s41431-021-01000-x
DO - 10.1038/s41431-021-01000-x
M3 - Editorial
C2 - 34916614
VL - 30
SP - 493
EP - 495
JO - European Journal of Human Genetics
JF - European Journal of Human Genetics
SN - 1018-4813
IS - 5
ER -