Menu
Currency
GWAS Study

A Spanish-Portuguese GWAS of progressive supranuclear palsy reveals a novel risk locus in NFASC.

García-González P, Rodrigo Lara H, Compta Y et al.

40379966 PubMed ID
GWAS Study Type
3909 Participants
78 Views
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

GP
García-González P
RL
Rodrigo Lara H
CY
Compta Y
FM
Fernandez M
VD
van der Lee SJ
DR
de Rojas I
SL
Saiz L
PC
Painous C
CA
Camara A
ME
Muñoz E
MM
Marti MJ
VF
Valldeoriola F
PR
Puerta R
II
Illán-Gala I
PJ
Pagonabarraga J
DO
Dols-Icardo O
KJ
Kulisevsky J
FJ
Fortea J
LA
Lleó A
OC
Olivé C
DB
de Boer SCM
HM
Hulsman M
PY
Pijnenburg YAL
DB
Díaz Belloso R
ML
Muñoz-Delgado L
BR
Buiza Rueda D
GP
Gómez-Garre P
AI
Aldecoa I
AG
Aragonés G
HV
Hernandez Vara J
MM
Mendioroz M
PJ
Pérez-Tur J
VP
Visser PJ
DB
den Braber A
PJ
Papma JM
MM
Martín Montes Á
RE
Rodriguez-Rodriguez E
BJ
Blázquez-Folch J
MA
Miguel A
GF
García-Gutiérrez F
CA
Cano A
VS
Valero S
MM
Marquié M
CM
Capdevila-Bayo M
RM
Rosende-Roca M
QI
Quintela I
Carracedo Á
TL
Tàrraga L
RL
Real LM
RJ
Royo JL
EM
Erro ME
GC
Guerrero C
CT
Corte Torres D
BM
Blázquez-Estrada M
SM
San Millán B
TS
Teijeira S
VR
Vilas Rolan D
HI
Hernández I
SA
Sánchez-Soblechero A
DL
de la Casa-Fages B
SL
Serrano López S
BR
Baviera-Muñoz R
LA
Lavín A
TR
Taipa R
AG
Amer G
ME
Martinez-Saez E
FM
Fernández-Matarrubia M
LC
Lage-Martínez C
ÁV
Álvarez V
ML
Molina-Porcel L
HH
Holstege H
MP
Mir P
BO
Belbin O
BM
Boada M
FV
Fernández V
BM
Bullido MJ
RA
Rábano A
SP
Sánchez-Juan P
RA
Ruiz A
Chapter II

Abstract

Summary of the research findings

Progressive supranuclear palsy (PSP) is a rare 4-repeat tauopathy that causes behavioural, movement and cognitive abnormalities. We genotyped all available clinical and histopathological PSP cases in Spain and Portugal (N = 522), and conducted the largest PSP GWAS of the Iberian population to date. Genetic burden analysis revealed reduced diagnostic specificity in clinically diagnosed atypical PSP cases-when applying the 2017 MDS criteria-compared to Richardson's syndrome cases. We independently replicated eight PSP risk variants in seven known loci (MAPT, MOBP, EIF2AK3, STX6, SLCO1A2, DUSP10 and APOE), and identified a novel locus in NFASC/CNTN2 (rs12744678 C: OR[95%CI] = 0.83[0.78-0.89]; p = 4.15·10-08) after meta-analysis with a newly available Dutch cohort and publicly available summary statistics (3,099 PSP; 11,482 controls). Enrichment analysis and protein expression profiling highlighted oligodendrocyte function and myelination as likely contributors to PSP pathogenesis. Our findings broaden the genetic landscape of PSP and suggest potential therapeutic avenues focused on modulating neuron-oligodendrocyte interactions.

446 European ancestry cases, 3,463 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

3909
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Netherlands, Portugal, Spain
Recruitment Country
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

Independent AI summary of health and genetic findings from the published study

Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

AI Summary In Progress

Our AI-generated summary of this publication is being prepared. Please check back soon.