%0 Journal Article %1 Kaune2020-ev %A Kaune, Tom %A Ruffert, Claudia %A Hesselbarth, Nico %A Damm, Marko %A Krug, Sebastian %A Cardinal von Widdern, Julian %A Masson, Emmanuelle %A Chen, Jian-Min %A Rebours, Vinciane %A Buscail, Louis %A Férec, Claude %A Grützmann, Robert %A Te Morsche, Rene H M %A Drenth, Joost Ph %A Cavestro, Giulia Martina %A Zuppardo, Raffaella Alessia %A Saftoiu, Adrian %A Malecka-Panas, Ewa %A Głuszek, Stanislaw %A Bugert, Peter %A Lerch, Markus M %A Sendler, Matthias %A Weiss, Frank Ulrich %A Zou, Wen-Bin %A Deng, Shun-Jiang %A Liao, Zhuan %A Scholz, Markus %A Kirsten, Holger %A Hegyi, Peter %A Witt, Heiko %A Michl, Patrick %A Griesmann, Heidi %A Rosendahl, Jonas %D 2020 %I Elsevier BV %J Pancreatology %K Calcium; G-Protein Genetics; Inflammation; Pancreatitis coupled receptor; topic_lifescience %N 7 %P 1262--1267 %T Analysis of GPRC6A variants in different pancreatitis etiologies %V 20 %X BACKGROUND: The G-protein-coupled receptor Class C Group 6 Member A (GPRC6A) is activated by multiple ligands and is important for the regulation of calcium homeostasis. Extracellular calcium is capable to increase NLRP3 inflammasome activity of the innate immune system and deletion of this proinflammatory pathway mitigated pancreatitis severity in vivo. As such this pathway and the GPRC6A receptor is a reasonable candidate gene for pancreatitis. Here we investigated the prevalence of sequence variants in the GPRC6A locus in different pancreatitis aetiologies. METHODS: We selected 6 tagging SNPs with the SNPinfo LD TAG SNP Selection tool and the functional relevant SNP rs6907580 for genotyping. Cohorts from Germany, further European countries and China with up to 1,124 patients and 1,999 controls were screened for single SNPs with melting curve analysis. RESULTS: We identified an association of rs1606365(G) with alcoholic chronic pancreatitis in a German (odds ratio (OR) 0.76, 95\% confidence interval (CI) 0.65-0.89, p = 8 $\times$ 10-5) and a Chinese cohort (OR 0.78, 95\% CI 0.64-0.96, p = 0.02). However, this association was not replicated in a combined cohort of European patients (OR 1.18, 95\% CI 0.99-1.41, p = 0.07). Finally, no association was found with acute and non-alcoholic chronic pancreatitis. CONCLUSIONS: Our results support a potential role of calcium sensing receptors and inflammasome activation in alcoholic chronic pancreatitis development. As the functional consequence of the associated variant is unclear, further investigations might elucidate the relevant mechanisms.

@article{Kaune2020-ev, abstract = {BACKGROUND: The G-protein-coupled receptor Class C Group 6 Member A (GPRC6A) is activated by multiple ligands and is important for the regulation of calcium homeostasis. Extracellular calcium is capable to increase NLRP3 inflammasome activity of the innate immune system and deletion of this proinflammatory pathway mitigated pancreatitis severity in vivo. As such this pathway and the GPRC6A receptor is a reasonable candidate gene for pancreatitis. Here we investigated the prevalence of sequence variants in the GPRC6A locus in different pancreatitis aetiologies. METHODS: We selected 6 tagging SNPs with the SNPinfo LD TAG SNP Selection tool and the functional relevant SNP rs6907580 for genotyping. Cohorts from Germany, further European countries and China with up to 1,124 patients and 1,999 controls were screened for single SNPs with melting curve analysis. RESULTS: We identified an association of rs1606365(G) with alcoholic chronic pancreatitis in a German (odds ratio (OR) 0.76, 95\% confidence interval (CI) 0.65-0.89, p = 8 $\times$ 10-5) and a Chinese cohort (OR 0.78, 95\% CI 0.64-0.96, p = 0.02). However, this association was not replicated in a combined cohort of European patients (OR 1.18, 95\% CI 0.99-1.41, p = 0.07). Finally, no association was found with acute and non-alcoholic chronic pancreatitis. CONCLUSIONS: Our results support a potential role of calcium sensing receptors and inflammasome activation in alcoholic chronic pancreatitis development. As the functional consequence of the associated variant is unclear, further investigations might elucidate the relevant mechanisms.}, added-at = {2024-09-10T11:54:51.000+0200}, author = {Kaune, Tom and Ruffert, Claudia and Hesselbarth, Nico and Damm, Marko and Krug, Sebastian and Cardinal von Widdern, Julian and Masson, Emmanuelle and Chen, Jian-Min and Rebours, Vinciane and Buscail, Louis and F{\'e}rec, Claude and Gr{\"u}tzmann, Robert and Te Morsche, Rene H M and Drenth, Joost Ph and Cavestro, Giulia Martina and Zuppardo, Raffaella Alessia and Saftoiu, Adrian and Malecka-Panas, Ewa and G{\l}uszek, Stanislaw and Bugert, Peter and Lerch, Markus M and Sendler, Matthias and Weiss, Frank Ulrich and Zou, Wen-Bin and Deng, Shun-Jiang and Liao, Zhuan and Scholz, Markus and Kirsten, Holger and Hegyi, Peter and Witt, Heiko and Michl, Patrick and Griesmann, Heidi and Rosendahl, Jonas}, biburl = {https://puma.scadsai.uni-leipzig.de/bibtex/205d06225f0f10a073a60753ac804ce68/scadsfct}, interhash = {ea46ff1c1cefe1bc1d6130603cfdb86d}, intrahash = {05d06225f0f10a073a60753ac804ce68}, journal = {Pancreatology}, keywords = {Calcium; G-Protein Genetics; Inflammation; Pancreatitis coupled receptor; topic_lifescience}, language = {en}, month = oct, number = 7, pages = {1262--1267}, publisher = {Elsevier BV}, timestamp = {2024-09-10T12:00:15.000+0200}, title = {Analysis of {GPRC6A} variants in different pancreatitis etiologies}, volume = 20, year = 2020 }