diopathic 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 Pcombined=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.

The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north–south gradient among Europeans / Becker, Jessica; Haas, Stephan L; Mokrowiecka, Anna; Wasielica Berger, Justyna; Ateeb, Zeeshan; Bister, Jonna; Elbe, Peter; Kowalski, Marek; Gawron Kiszka, Magdalena; Majewski, Marek; Mulak, Agata; Janiak, Maria; Wouters, Mira M; Schwämmle, Till; Hess, Timo; Veits, Lothar; Niebisch, Stefan; Santiago, José L; de León, Antonio Ruiz; de la Serna, Julio Pérez; Urcelay, Elena; Annese, Vito; Latiano, Anna; Fumagalli, Uberto; Rosati, Riccardo; Laghi, Luigi; Cuomo, Rosario; Lenze, Frank; Sarnelli, Giovanni; Müller, Michaela; von Rahden, Burkhard HA; Wijmenga, Cisca; Lang, Hauke; Czene, Kamila; Hall, Per; de Bakker, Paul IW; Vieth, Michael; Nöthen, Markus M; Schulz, Henning G; Adrych, Krystian; Gąsiorowska, Anita; Paradowski, Leszek; Wallner, Grzegorz; Boeckxstaens, Guy E; Gockel, Ines; Hartleb, Marek; Kostic, Srdjan; Dziurkowska Marek, Anna; Lindblad, Mats; Nilsson, Magnus; Knapp, Michael; Thorell, Anders; Marek, Tomasz; Dąbrowski, Andrzej; Małecka Panas, Ewa; Schumacher, Johannes. - In: EUROPEAN JOURNAL OF HUMAN GENETICS. - ISSN 1018-4813. - 24:8(2016), pp. 1228-1231. [10.1038/ejhg.2015.262]

The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north–south gradient among Europeans

CUOMO, ROSARIO;SARNELLI, GIOVANNI;
2016

Abstract

diopathic 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 Pcombined=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.
2016
The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north–south gradient among Europeans / Becker, Jessica; Haas, Stephan L; Mokrowiecka, Anna; Wasielica Berger, Justyna; Ateeb, Zeeshan; Bister, Jonna; Elbe, Peter; Kowalski, Marek; Gawron Kiszka, Magdalena; Majewski, Marek; Mulak, Agata; Janiak, Maria; Wouters, Mira M; Schwämmle, Till; Hess, Timo; Veits, Lothar; Niebisch, Stefan; Santiago, José L; de León, Antonio Ruiz; de la Serna, Julio Pérez; Urcelay, Elena; Annese, Vito; Latiano, Anna; Fumagalli, Uberto; Rosati, Riccardo; Laghi, Luigi; Cuomo, Rosario; Lenze, Frank; Sarnelli, Giovanni; Müller, Michaela; von Rahden, Burkhard HA; Wijmenga, Cisca; Lang, Hauke; Czene, Kamila; Hall, Per; de Bakker, Paul IW; Vieth, Michael; Nöthen, Markus M; Schulz, Henning G; Adrych, Krystian; Gąsiorowska, Anita; Paradowski, Leszek; Wallner, Grzegorz; Boeckxstaens, Guy E; Gockel, Ines; Hartleb, Marek; Kostic, Srdjan; Dziurkowska Marek, Anna; Lindblad, Mats; Nilsson, Magnus; Knapp, Michael; Thorell, Anders; Marek, Tomasz; Dąbrowski, Andrzej; Małecka Panas, Ewa; Schumacher, Johannes. - In: EUROPEAN JOURNAL OF HUMAN GENETICS. - ISSN 1018-4813. - 24:8(2016), pp. 1228-1231. [10.1038/ejhg.2015.262]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/633508
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