Assessing the binding interaction of polystyrene sulfonate with amitriptyline in healthy volunteers

Autor: I. Prins - Can, I. R. F. van Berlo - van de Laar, M. Zeeman, C. G. Vermeij, E. van ’t Riet, K. Taxis, F. G. A. Jansman

Publikováno v: European Journal of Clinical Pharmacology, 78(5), 839-845. Springer Verlag

Purpose: Polystyrene sulfonate is used for binding potassium in patients with chronic kidney disease (CKD). Because of its binding properties, it can potentially bind other medications and thereby decrease their bioavailability and effectiveness. Ami

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06908e68cb41e3714cfcc2b2bdab10ed
https://research.rug.nl/en/publications/09fd9065-27ae-47b2-b2c6-25089790df25

Assessing the binding interaction of polystyrene sulfonate with amitriptyline in healthy volunteers: a cross-over design - The BIND study

Autor: I, Prins-Can, I R F, van Berlo-van de Laar, M, Zeeman, C G, Vermeij, E, van 't Riet, K, Taxis, F G A, Jansman

Publikováno v: European journal of clinical pharmacology. 78(5)

Polystyrene sulfonate is used for binding potassium in patients with chronic kidney disease (CKD). Because of its binding properties, it can potentially bind other medications and thereby decrease their bioavailability and effectiveness. Amitriptylin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ec4fbed4640a2dcb321708bd849b9998
https://pubmed.ncbi.nlm.nih.gov/35171315

Combined effects of single-nucleotide polymorphisms in GCK, GCKR, G6PC2 and MTNR1B on fasting plasma glucose and type 2 diabetes risk

Autor: E. C. van Hove, Marlous J. Groenewoud, E. van 't Riet, Johannes A Maassen, L.M.C. Welschen, Erwin Reiling, Leen M 't Hart, J. M. Dekker, Giel Nijpels

Publikováno v: Diabetologia, 52(9), 1866-1870. Springer Verlag
Diabetologia
Reiling, E, van 't Riet, E, Groenewoud, M J, Welschen, L M C, van Hove, E C, Nijpels, M G A A M, Maassen, J A, Dekker, J M & Hart, L M 2009, ' Combined effects of single-nucleotide polymorphisms in GCK, GCKR, G6PC2 and MTNR1B on fasting plasma glucose and type 2 diabetes risk ', Diabetologia, vol. 52, no. 9, pp. 1866-1870 . https://doi.org/10.1007/s00125-009-1413-9

Aims/hypothesis Variation in fasting plasma glucose (FPG) within the normal range is a known risk factor for the development of type 2 diabetes. Several reports have shown that genetic variation in the genes for glucokinase (GCK), glucokinase regulat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6aaa03e7ab42721f5c0783cd5f0ba1ed
https://doi.org/10.1007/s00125-009-1413-9

Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes

Autor: M. Tang, S. Y. Kim, Tom Forsén, Yun Li, Q. Li, Karina Banasik, J. M. Dekker, Leif Groop, B. Balkau, N. van Leeuwen, Jacek Mokrosinski, G. Tian, Alex S. F. Doney, Thue W. Schwartz, H. Jiang, Johanna Kuusisto, Thorfinn Sand Korneliussen, S. Huang, Guillaume Charpentier, Giel Nijpels, Daniel R. Witte, Maria Lajer, Alena Stančáková, F. Xi, Oluf Pedersen, Anders Albrechtsen, Torben Jørgensen, Mozhgan Dorkhan, Torben Hansen, Amanda J. Bennett, B. Wang, Gregers S. Andersen, Chang Yu, Aneta Aleksandra Nielsen, Mark I. McCarthy, Lise Tarnow, Markku Laakso, Timothy M. Frayling, P.E. Slagboom, Olov Rolandsson, Y. Wang, Torsten Lauritzen, Christopher J. Groves, Weihua Zhang, Peter M. Nilsson, T. Jiang, Loic Yengo, Leen M 't Hart, Y. Gui, Tiinamaija Tuomi, Chao Nie, Peter Rossing, J. Zhang, Frida Renström, Andrew D. Morris, Cramer Christensen, Graham A. Hitman, Neil Robertson, H. Cao, Göran Hallmans, Allan Linneberg, Niels Grarup, Line Skotte, H. Wu, Colin N. A. Palmer, M. P. Manijak, Q. Zhang, Andrew P. Morris, Rasmus Ribel-Madsen, Yi Chen, Arne Astrup, Tibor V. Varga, Mark Walker, Y. Zhou, Jun Wang, Maria Sterner, Paul W. Franks, Lars Bolund, Andrew T. Hattersley, Johan Holmkvist, Karsten Kristiansen, David Altshuler, E. van 't Riet, Philippe Froguel, Stéphane Cauchi, R. Wu, Kunlun He, B. Mu, X. Ma, X. Liu, Weijing Li, H. Liang, Rasmus Nielsen, Olivier Lantieri, T. Ma, Xin Jin, Claes Ladenvall, Michel Marre, Nigel W. Rayner, Thomas Sparsø, Marie A. Vestmar, Johanne Marie Justesen, Ivan Brandslund, Q. Liao, Xiaoming Zhang, H. Zheng

Publikováno v: Diabetologia
Diabetologia, 56(2), 298-310. Springer Verlag
Albrechtsen, A, Grarup, N, Li, Y, Sparsø, T H, Tian, G, Cao, H, Jiang, T, Kim, S Y, Korneliussen, T S, Li, Q, Nie, C, Wu, R, Skotte, L, Morris, A P, Ladenvall, C, Cauchi, S, Stancáková, A, Andersen, G, Astrup, A, Banasik, K, Bennett, A J, Bolund, L, Charpentier, G, Chen, Y, Dekker, J M, Doney, A S F, Dorkhan, M, Forsen, T, Frayling, T M, Groves, C J, Gui, Y, Hallmans, G, Hattersley, A T, He, K, Hitman, G A, Holmkvist, J, Huang, S, Jiang, H, Jin, X, Justesen, J M, Kristiansen, K, Kuusisto, J, Lajer, M, Lantieri, O, Li, W, Liang, H, Liao, Q, Liu, X, Ma, T, Ma, X, Manijak, M P, Marre, M, Mokrosinski, J, Morris, A D, Mu, B, Nielsen, A A, Nijpels, G, Nilsson, P, Palmer, C N A, Rayner, N W, Renström, F, Ribel-Madsen, R, Robertson, N, Rolandsson, O, Rossing, P, Schwartz, T W, Slagboom, P E, Sterner, M, Tang, M, Tarnow, L, Tuomi, T, Van't Riet, E, van Leeuwen, N, Varga, T V, Vestmar, M A, Walker, M, Wang, B, Wang, Y, Wu, H, Xi, F, Yengo, L, Yu, C, Zhang, X, Zhang, J, Zhang, Q, Zhang, W, Zheng, H, Zhou, Y, Altshuler, D, 't Hart, L M, Franks, P W, Balkau, B, Froguel, P, McCarthy, M I, Laakso, M, Groop, L, Christensen, C, Brandslund, I, Lauritzen, T, Witte, D R, Linneberg, A, Jørgensen, T, Hansen, T, Wang, J, Nielsen, R & Pedersen, O 2013, ' Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes ', Diabetologia, vol. 56, no. 2, pp. 298-310 . https://doi.org/10.1007/s00125-012-2756-1
Albrechtsen, A, Grarup, N, Li, Y, Sparsø, T H, Tian, G, Cao, H, Jiang, T, Kim, S Y, Korneliussen, T, Li, Q, Nie, C, Wu, R, Skotte, L, Morris, A P, Ladenvall, C, Cauchi, S, Stančáková, A, Andersen, G, Astrup, A, Banasik, K, Bennett, A J, Bolund, L, Charpentier, G, Chen, Y, Dekker, J M, Doney, A S F, Dorkhan, M, Forsen, T, Frayling, T M, Groves, C J, Gui, Y, Hallmans, G, Hattersley, A T, He, K, Hitman, G A, Holmkvist, J, Huang, S, Jiang, H, Jin, X, Justesen, J M, Kristiansen, K, Kuusisto, J, Lajer, M, Lantieri, O, Li, W, Liang, H, Liao, Q, Nielsen, A A, Christensen, C, Brandslund, I & D.E.S.I.R. Study Group 2013, ' Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes ', Diabetologia, vol. 56, no. 2, pp. 298-310 . https://doi.org/10.1007/s00125-012-2756-1
Albrechtsen, A, Grarup, N, Li, Y, Sparso, T, Tian, G, Cao, H, Jiang, T, Kim, S Y, Korneliussen, T, Li, Q, Nie, C, Wu, R, Skotte, L, Morris, A P, Ladenvall, C, Cauchi, S, Stancakova, A, Andersen, G, Astrup, A, Banasik, K, Bennett, A J, Bolund, L, Charpentier, G, Chen, Y, Dekker, J M, Doney, A S F, Dorkhan, M, Forsen, T, Frayling, T M, Groves, C J, Gui, Y, Hallmans, G, Hattersley, A T, He, K, Hitman, G A, Holmkvist, J, Huang, S, Jiang, H, Jin, X, Justesen, J M, Kristiansen, K, Kuusisto, J, Lajer, M, Lantieri, O, Li, W, Liang, H, Liao, Q, Liu, X, Ma, T, Ma, X, Manijak, M P, Marre, M, Mokrosinski, J, Morris, A D, Mu, B, Nielsen, A A, Nijpels, G, Nilsson, P, Palmer, C N A, Rayner, N W, Renström, F, Ribel-Madsen, R, Robertson, N, Rolandsson, O, Rossing, P, Schwartz, T W, Slagboom, P E, Sterner, M, Tang, M, Tarnow, L, Tuomi, T, van't Riet, E, van Leeuwen, N, Varga, T V, Vestmar, M A, Walker, M, Wang, B, Wang, Y, Wu, H, Xi, F, Yengo, L, Yu, C, Zhang, X, Zhang, J, Zhang, Q, Zhang, W, Zheng, H, Zhou, Y, Altshuler, D, 't Hart, L M, Franks, P W, Balkau, B, Froguel, P, McCarthy, M I, Laakso, M, Groop, L, Christensen, C, Brandslund, I, Lauritzen, T, Witte, D R, Linneberg, A, Jørgensen, T, Hansen, T, Wang, J, Nielsen, R & Pedersen, O 2013, ' Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes ', Diabetologia, vol. 56, no. 2, pp. 298-310 . https://doi.org/10.1007/s00125-012-2756-1
Diabetologia; Vol 56
Diabetologia, 56(2), 298-310. SPRINGER
Albrechtsen, A, Grarup, N, Li, Y, Sparsø, T H, Tian, G, Cao, H, Jiang, T, Kim, S Y, Korneliussen, T S, Li, Q, Nie, C, Wu, R, Skotte, L, Morris, A P, Ladenvall, C, Cauchi, S, Stančáková, A, Andersen, G, Astrup, A, Banasik, K, Bennett, A J, Bolund, L, Charpentier, G, Chen, Y, Dekker, J M, Doney, A S F, Dorkhan, M, Forsen, T, Frayling, T M, Groves, C J, Gui, Y, Hallmans, G, Hattersley, A T, He, K, Hitman, G A, Holmkvist, J, Huang, S, Jiang, H, Jin, X, Justesen, J M, Kristiansen, K, Kuusisto, J, Lajer, M, Lantieri, O, Li, W, Liang, H, Liao, Q, Liu, X, Lauritzen, T, Pedersen, O & D.E.S.I.R. Study Group 2013, ' Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes ', Diabetologia, vol. 56, no. 2, pp. 298-310 . https://doi.org/10.1007/s00125-012-2756-1
PMC
Albrechtsen, A, Grarup, N, Li, Y, Sparso, T, Tian, G, Cao, H, Jiang, T, Kim, S Y, Korneliussen, T, Li, Q, Nie, C, Wu, R, Skotte, L, Morris, A P, Ladenvall, C, Cauchi, S, Stancakova, A, Andersen, G, Astrup, A, Banasik, K, Bennett, A J, Bolund, L, Charpentier, G, Chen, Y, Dekker, J M, Doney, A S F, Dorkhan, M, Forsen, T, Frayling, T M, Groves, C J, Gui, Y, Hallmans, G, Hattersley, A T, He, K, Hitman, G A, Holmkvist, J, Huang, S, Jiang, H, Jin, X, Justesen, J M, Kristiansen, K, Kuusisto, J, Lajer, M, Lantieri, O, Li, W, Liang, H, Liao, Q, Liu, X, Ma, T, Ma, X, Manijak, M P, Marre, M, Mokrosinski, J, Morris, A D, Mu, B, Nielsen, A A, Nijpels, G, Nilsson, P, Palmer, C N A, Rayner, N W, Renstrom, F, Ribel-Madsen, R, Robertson, N, Rolandsson, O, Rossing, P, Schwartz, T W, Slagboom, P E, Sterner, M, Tang, M, Tarnow, L, Tuomi, T, van 't Riet, E, van Leeuwen, N, Varga, T V, Vestmar, M A, Walker, M, Wang, B, Wang, Y, Wu, H, Xi, F, Yengo, L, Yu, C, Zhang, X, Zhang, J, Zhang, Q, Zhang, W, Zheng, H, Zhou, Y, Altshuler, D, 't Hart, L M, Franks, P W, Balkau, B, Froguel, P, McCarthy, M I, Laakso, M, Groop, L, Christensen, C, Brandslund, I, Lauritzen, T, Witte, D R, Linneberg, A, Jorgensen, T, Hansen, T, Wang, J, Nielsen, R & Pedersen, O 2013, ' Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes ', Diabetologia, vol. 56, no. 2, pp. 298-310 . https://doi.org/10.1007/s00125-012-2756-1
Diabetologia, 56(2), 298-310

Aims/hypothesis Human complex metabolic traits are in part regulated by genetic determinants. Here we applied exome sequencing to identify novel associations of coding polymorphisms at minor allele frequencies (MAFs) >1% with common metabolic phenoty

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3128dab4992f848b73aa70c05e385e9
http://europepmc.org/articles/PMC3536959

A gene variant near ATM is significantly associated with metformin treatment response in type 2 diabetes: a replication and meta-analysis of five cohorts

Autor: Giel Nijpels, Paul N. Durrington, J.M. Dekker, Harshal Deshmukh, A. Hofman, Helen M. Colhoun, Rury R. Holman, Bruno Guigas, Graham A. Hitman, N. van Leeuwen, Roberto A. Calle, Ke Zhou, E. van 't Riet, Christopher R. Palmer, Ewan R. Pearson, B. H. Stricker, Andrew Neil, Matthijs L. Becker, Shona J. Livingstone, P.E. Slagboom, A.G. Uitterlinden, Leen M 't Hart, Mark I. McCarthy

Publikováno v: Diabetologia, 55(7), 1971-1977. Springer-Verlag
Diabetologia
van Leeuwen, N, Nijpels, G, Becker, M L, Deshmukh, H, Zhou, K, Stricker, B H C, Uitterlinden, A G, Hofman, A, van 't Riet, E, Palmer, C N A, Guigas, B, Slagboom, P E, Durrington, P, Calle, R A, Neil, A, Hitman, G, Livingstone, S J, Colhoun, H, Holman, R R, McCarthy, M I, Dekker, J M, Hart, L M & Pearson, E R 2012, ' A gene variant near ATM is significantly associated with metformin treatment response in type 2 diabetes: a replication and meta-analysis of five cohorts ', Diabetologia, vol. 55, no. 7, pp. 1971-1977 . https://doi.org/10.1007/s00125-012-2537-x
Diabetologia, 55(7), 1971-1977. Springer Verlag
Diabetologia, 55(7), 1971-1977

Aims/hypothesis In this study we aimed to replicate the previously reported association between the glycaemic response to metformin and the SNP rs11212617 at a locus that includes the ataxia telangiectasia mutated (ATM) gene in multiple additional po

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::776b6e36d40f6f29f60f7911a45f31fc
https://hdl.handle.net/1765/69013