Common inflammation-related candidate gene variants and acute kidney injury in 2647 critically ill Finnish patients

Abstract Acute kidney injury (AKI) is a syndrome with high incidence among the critically ill. Because the clinical variables and currently used biomarkers have failed to predict the individual susceptibility to AKI, candidate gene variants for the trait have been studied. Studies about genetic pred...

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Main Authors: Vilander, L. M. (Laura M.), Vaara, S. T. (Suvi T.), Kaunisto, M. A. (Mari A.), Pettilä, V. (Ville), T. F. (The FINNAKI Study Group)
Format: Article in Journal/Newspaper
Language:English
Published: Multidisciplinary Digital Publishing Institute 2019
Subjects:
Ari
Online Access:http://urn.fi/urn:nbn:fi-fe2019100831666
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collection Jultika - University of Oulu repository
op_collection_id ftunivoulu
language English
topic acute kidney injury
genetic variation
human genetics
spellingShingle acute kidney injury
genetic variation
human genetics
Vilander, L. M. (Laura M.)
Vaara, S. T. (Suvi T.)
Kaunisto, M. A. (Mari A.)
Pettilä, V. (Ville)
T. F. (The FINNAKI Study Group)
Common inflammation-related candidate gene variants and acute kidney injury in 2647 critically ill Finnish patients
topic_facet acute kidney injury
genetic variation
human genetics
description Abstract Acute kidney injury (AKI) is a syndrome with high incidence among the critically ill. Because the clinical variables and currently used biomarkers have failed to predict the individual susceptibility to AKI, candidate gene variants for the trait have been studied. Studies about genetic predisposition to AKI have been mainly underpowered and of moderate quality. We report the association study of 27 genetic variants in a cohort of Finnish critically ill patients, focusing on the replication of associations detected with variants in genes related to inflammation, cell survival, or circulation. In this prospective, observational Finnish Acute Kidney Injury (FINNAKI) study, 2647 patients without chronic kidney disease were genotyped. We defined AKI according to Kidney Disease: Improving Global Outcomes (KDIGO) criteria. We compared severe AKI (Stages 2 and 3, n = 625) to controls (Stage 0, n = 1582). For genotyping we used iPLEX™ Assay (Agena Bioscience). We performed the association analyses with PLINK software, using an additive genetic model in logistic regression. Despite the numerous, although contradictory, studies about association between polymorphisms rs1800629 in TNFA and rs1800896 in IL10 and AKI, we found no association (odds ratios 1.06 (95% CI 0.89–1.28, p = 0.51) and 0.92 (95% CI 0.80–1.05, p = 0.20), respectively). Adjusting for confounders did not change the results. To conclude, we could not confirm the associations reported in previous studies in a cohort of critically ill patients. Acknowledgements We thank the FINNAKI Study Group Members: Central Finland Central Hospital: Raili Laru-Sompa, Anni Pulkkinen, Minna Saarelainen, Mikko Reilama, Sinikka Tolmunen, Ulla Rantalainen, Marja Miettinen; East Savo Central Hospital: Markku Suvela, Katrine Pesola, Pekka Saastamoinen, Sirpa Kauppinen; Helsinki University Central Hospital: Ville Pettilä, Kirsi-Maija Kaukonen, Anna-Maija Korhonen, Sara Nisula, Suvi Vaara, Raili Suojaranta-Ylinen, Leena Mildh, Mikko Haapio, Laura Nurminen, Sari Sutinen, Leena Pettilä, Helinä Laitinen, Heidi Syrjä, Kirsi Henttonen, Elina Lappi, Hillevi Boman; Jorvi Central Hospital: Tero Varpula, Päivi Porkka, Mirka Sivula, Mira Rahkonen, Anne Tsurkka, Taina Nieminen, Niina Prittinen; KantaHäme Central Hospital: Ari Alaspää, Ville Salanto, Hanna Juntunen, Teija Sanisalo; Kuopio University Hospital: Ilkka Parviainen, Ari Uusaro, Esko Ruokonen, Stepani Bendel, Niina Rissanen, Maarit Lång, Sari Rahikainen, Saija Rissanen, Merja Ahonen, Elina Halonen, Eija Vaskelainen; Lapland Central Hospital: Meri Poukkanen, Esa Lintula, Sirpa Suominen; Länsi Pohja Central Hospital: Jorma Heikkinen, Timo Lavander, Kirsi Heinonen, Anne-Mari Juopperi; Middle Ostrobothnia Central Hospital: Tadeusz Kaminski, Fiia Gäddnäs, Tuija Kuusela, Jane Roiko; North Karelia Central Hospital: Sari Karlsson, Matti Reinikainen, Tero Surakka, Helena Jyrkönen, Tanja Eiserbeck, Jaana Kallinen; Satakunta Hospital District: Vesa Lund, Päivi Tuominen, Pauliina Perkola, Riikka Tuominen, Marika Hietaranta, Satu Johansson; South Karelia Central Hospital: Seppo Hovilehto, Anne Kirsi, Pekka Tiainen, Tuija Myllärinen, Pirjo Leino, Anne Toropainen; Tampere University Hospital: Anne Kuitunen, Ilona Leppänen, Markus Levoranta, Sanna Hoppu, Jukka Sauranen, Jyrki Tenhunen, Atte Kukkurainen, Samuli Kortelainen, Simo Varila; Turku University Hospital: Outi Inkinen, Niina Koivuviita, Jutta Kotamäki, Anu Laine; Oulu University Hospital: Tero Ala-Kokko, Jouko Laurila, Sinikka Sälkiö; Vaasa Central Hospital: Simo-Pekka Koivisto, Raku Hautamäki, Maria Skinnar.
format Article in Journal/Newspaper
author Vilander, L. M. (Laura M.)
Vaara, S. T. (Suvi T.)
Kaunisto, M. A. (Mari A.)
Pettilä, V. (Ville)
T. F. (The FINNAKI Study Group)
author_facet Vilander, L. M. (Laura M.)
Vaara, S. T. (Suvi T.)
Kaunisto, M. A. (Mari A.)
Pettilä, V. (Ville)
T. F. (The FINNAKI Study Group)
author_sort Vilander, L. M. (Laura M.)
title Common inflammation-related candidate gene variants and acute kidney injury in 2647 critically ill Finnish patients
title_short Common inflammation-related candidate gene variants and acute kidney injury in 2647 critically ill Finnish patients
title_full Common inflammation-related candidate gene variants and acute kidney injury in 2647 critically ill Finnish patients
title_fullStr Common inflammation-related candidate gene variants and acute kidney injury in 2647 critically ill Finnish patients
title_full_unstemmed Common inflammation-related candidate gene variants and acute kidney injury in 2647 critically ill Finnish patients
title_sort common inflammation-related candidate gene variants and acute kidney injury in 2647 critically ill finnish patients
publisher Multidisciplinary Digital Publishing Institute
publishDate 2019
url http://urn.fi/urn:nbn:fi-fe2019100831666
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op_rights info:eu-repo/semantics/openAccess
© 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
https://creativecommons.org/licenses/by/4.0/
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spelling ftunivoulu:oai:oulu.fi:nbnfi-fe2019100831666 2023-05-15T17:00:29+02:00 Common inflammation-related candidate gene variants and acute kidney injury in 2647 critically ill Finnish patients Vilander, L. M. (Laura M.) Vaara, S. T. (Suvi T.) Kaunisto, M. A. (Mari A.) Pettilä, V. (Ville) T. F. (The FINNAKI Study Group) 2019 application/pdf http://urn.fi/urn:nbn:fi-fe2019100831666 eng eng Multidisciplinary Digital Publishing Institute info:eu-repo/semantics/openAccess © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). https://creativecommons.org/licenses/by/4.0/ CC-BY acute kidney injury genetic variation human genetics info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion 2019 ftunivoulu 2021-06-25T17:54:58Z Abstract Acute kidney injury (AKI) is a syndrome with high incidence among the critically ill. Because the clinical variables and currently used biomarkers have failed to predict the individual susceptibility to AKI, candidate gene variants for the trait have been studied. Studies about genetic predisposition to AKI have been mainly underpowered and of moderate quality. We report the association study of 27 genetic variants in a cohort of Finnish critically ill patients, focusing on the replication of associations detected with variants in genes related to inflammation, cell survival, or circulation. In this prospective, observational Finnish Acute Kidney Injury (FINNAKI) study, 2647 patients without chronic kidney disease were genotyped. We defined AKI according to Kidney Disease: Improving Global Outcomes (KDIGO) criteria. We compared severe AKI (Stages 2 and 3, n = 625) to controls (Stage 0, n = 1582). For genotyping we used iPLEX™ Assay (Agena Bioscience). We performed the association analyses with PLINK software, using an additive genetic model in logistic regression. Despite the numerous, although contradictory, studies about association between polymorphisms rs1800629 in TNFA and rs1800896 in IL10 and AKI, we found no association (odds ratios 1.06 (95% CI 0.89–1.28, p = 0.51) and 0.92 (95% CI 0.80–1.05, p = 0.20), respectively). Adjusting for confounders did not change the results. To conclude, we could not confirm the associations reported in previous studies in a cohort of critically ill patients. Acknowledgements We thank the FINNAKI Study Group Members: Central Finland Central Hospital: Raili Laru-Sompa, Anni Pulkkinen, Minna Saarelainen, Mikko Reilama, Sinikka Tolmunen, Ulla Rantalainen, Marja Miettinen; East Savo Central Hospital: Markku Suvela, Katrine Pesola, Pekka Saastamoinen, Sirpa Kauppinen; Helsinki University Central Hospital: Ville Pettilä, Kirsi-Maija Kaukonen, Anna-Maija Korhonen, Sara Nisula, Suvi Vaara, Raili Suojaranta-Ylinen, Leena Mildh, Mikko Haapio, Laura Nurminen, Sari Sutinen, Leena Pettilä, Helinä Laitinen, Heidi Syrjä, Kirsi Henttonen, Elina Lappi, Hillevi Boman; Jorvi Central Hospital: Tero Varpula, Päivi Porkka, Mirka Sivula, Mira Rahkonen, Anne Tsurkka, Taina Nieminen, Niina Prittinen; KantaHäme Central Hospital: Ari Alaspää, Ville Salanto, Hanna Juntunen, Teija Sanisalo; Kuopio University Hospital: Ilkka Parviainen, Ari Uusaro, Esko Ruokonen, Stepani Bendel, Niina Rissanen, Maarit Lång, Sari Rahikainen, Saija Rissanen, Merja Ahonen, Elina Halonen, Eija Vaskelainen; Lapland Central Hospital: Meri Poukkanen, Esa Lintula, Sirpa Suominen; Länsi Pohja Central Hospital: Jorma Heikkinen, Timo Lavander, Kirsi Heinonen, Anne-Mari Juopperi; Middle Ostrobothnia Central Hospital: Tadeusz Kaminski, Fiia Gäddnäs, Tuija Kuusela, Jane Roiko; North Karelia Central Hospital: Sari Karlsson, Matti Reinikainen, Tero Surakka, Helena Jyrkönen, Tanja Eiserbeck, Jaana Kallinen; Satakunta Hospital District: Vesa Lund, Päivi Tuominen, Pauliina Perkola, Riikka Tuominen, Marika Hietaranta, Satu Johansson; South Karelia Central Hospital: Seppo Hovilehto, Anne Kirsi, Pekka Tiainen, Tuija Myllärinen, Pirjo Leino, Anne Toropainen; Tampere University Hospital: Anne Kuitunen, Ilona Leppänen, Markus Levoranta, Sanna Hoppu, Jukka Sauranen, Jyrki Tenhunen, Atte Kukkurainen, Samuli Kortelainen, Simo Varila; Turku University Hospital: Outi Inkinen, Niina Koivuviita, Jutta Kotamäki, Anu Laine; Oulu University Hospital: Tero Ala-Kokko, Jouko Laurila, Sinikka Sälkiö; Vaasa Central Hospital: Simo-Pekka Koivisto, Raku Hautamäki, Maria Skinnar. Article in Journal/Newspaper karelia* Lapland Lappi Jultika - University of Oulu repository Ari ENVELOPE(147.813,147.813,59.810,59.810) Halonen ENVELOPE(27.500,27.500,66.683,66.683) Heikkinen ENVELOPE(24.450,24.450,66.550,66.550) Heinonen ENVELOPE(22.600,22.600,67.167,67.167) Jukka ENVELOPE(24.917,24.917,67.650,67.650) Kaukonen ENVELOPE(24.898,24.898,67.481,67.481) Kauppinen ENVELOPE(20.467,20.467,67.833,67.833) Koivisto ENVELOPE(26.486,26.486,67.052,67.052) Korhonen ENVELOPE(28.850,28.850,65.950,65.950) Lintula ENVELOPE(25.983,25.983,66.300,66.300) Mira ENVELOPE(10.500,10.500,-70.417,-70.417) Parviainen ENVELOPE(23.848,23.848,65.886,65.886) Pekka ENVELOPE(23.816,23.816,66.180,66.180) Saija ENVELOPE(28.817,28.817,67.089,67.089) Sanna ENVELOPE(12.047,12.047,66.506,66.506) Simo ENVELOPE(25.061,25.061,65.663,65.663) Ulla ENVELOPE(6.192,6.192,62.679,62.679) Vaara ENVELOPE(24.886,24.886,67.360,67.360) Vesa ENVELOPE(23.583,23.583,67.633,67.633) Ylinen ENVELOPE(20.383,20.383,67.783,67.783)