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THE HLA-DQΒ1 INSERTION IS A STRONG ACHALASIA RISK FACTOR AND DISPLAYS A GEOSPATIAL NORTH-SOUTH GRADIENT AMONG EUROPEANS

Academic Article
Publication Date:
2016
abstract:
Idiopathic achalasia is a severe motility disorder of the esophagus and is characterized by a failure of the lower esophageal sphincter to relax due to a loss of neurons in the myenteric plexus. Most recently, we identified an eight-amino-acid insertion in the cytoplasmic tail of HLA-DQβ1 as strong achalasia risk factor in a sample set from Central Europe, Italy and Spain. Here, we tested whether the HLA-DQβ1 insertion also confers achalasia risk in the Polish and Swedish population. We could replicate the initial findings and the insertion shows strong achalasia association in both samples (Poland P=1.84 × 10 -04, Sweden P=7.44 × 10 -05). Combining all five European data sets - Central Europe, Italy, Spain, Poland and Sweden - the insertion is achalasia associated with P combined =1.67 × 10 -35. In addition, we observe that the frequency of the insertion shows a geospatial north-south gradient. The insertion is less common in northern (around 6-7% in patients and 2% in controls from Sweden and Poland) compared with southern Europeans (∼16% in patients and 8% in controls from Italy) and shows a stronger attributable risk in the southern European population. Our study provides evidence that the prevalence of achalasia may differ between populations.
Iris type:
1.1 Articolo in rivista
Keywords:
Esophageal Achalasia; Europe; European Continental Ancestry Group; Female; HLA-DQ beta-Chains; Humans; Male; Mutation Rate; Polymorphism, Genetic; Prevalence; Mutagenesis, Insertional; Genetics; Genetics (clinical)
List of contributors:
Schumacher, J; Becker, J; Haas, S; Mokrowiecka, A; Wasielica Berger, J; Ateeb, Z; Bister, J; Elbe, P; Kowalski, M; Gawron Kiszka, M; Majewski, M; Mulak, A; Janiak, M; Wouters, M; Schwämmle, T; Hess, T; Veits, L; Niebisch, S; Santiago, Jl; Ruiz de León, A; Pérez de la Serna, J; Urcelay, E; Annese, V; Latiano, A; Fumagalli, U; Rosati, Riccardo; Laghi, L; Cuomo, R; Lenze, F; Sarnelli, G; Müller, M; von Rahden, B; Wijmenga, C; Lang, H; Czene, K; Hall, P; de Bakker, P; Vieth, M; Nöthen, M; Schulz, H; Adrych, K; Gąsiorowska, A; Paradowski, L; Wallner, G; Boeckxstaens, G; Gockel, I; Hartleb, M; Kostic, S; Dziurkowska Marek, A; Lindblad, ; Nilsson, M; Knapp, M; Thorell, A; Marek, T; Dąbrowski, A; Małecka Panas, E.
Authors of the University:
ANNESE VITO
ROSATI RICCARDO
Handle:
https://iris.unisr.it/handle/20.500.11768/12577
Published in:
EUROPEAN JOURNAL OF HUMAN GENETICS
Journal
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