Search: onr:"swepub:oai:gup.ub.gu.se/285373" >
New candidate genes...
-
Cederstrom, S.Karolinska Institutet
(author)
New candidate genes for ST-elevation myocardial infarction
- Article/chapterEnglish2020
Publisher, publication year, extent ...
Numbers
-
LIBRIS-ID:oai:gup.ub.gu.se/285373
-
https://gup.ub.gu.se/publication/285373URI
-
https://doi.org/10.1111/joim.12976DOI
-
http://kipublications.ki.se/Default.aspx?queryparsed=id:141991367URI
Supplementary language notes
Part of subdatabase
Classification
-
Subject category:ref swepub-contenttype
-
Subject category:art swepub-publicationtype
Notes
-
Background Despite extensive research in atherosclerosis, the mechanisms of coronary atherothrombosis in ST-elevation myocardial infarction (STEMI) patients are undetermined. Objectives Our aim was to find candidate genes involved in STEMI by analysing leucocyte gene expression in STEMI patients, without the influence of secondary inflammation from innate immunity, which was assumed to be a consequence rather than the cause of coronary atherothrombosis. Methods Fifty-one patients were included at coronary angiography because of STEMI. Arterial blood was sampled in the acute phase (P1), at 24-48 h (P2) and at 3 months (P3). Leucocyte RNA was isolated and gene expression analysis was performed by Affymetrix Human Transcriptome Array 2.0. By omission of up- or downregulated genes at P2, secondary changes from innate immunity were excluded. Genes differentially expressed in P1 when compared to the convalescent sample in P3 were determined as genes involved in STEMI. Results Three genes were upregulated at P1 compared to P3; ABCG1 (P = 5.81 x 10(-5)), RAB20 (P = 3.69 x 10(-5)) and TMEM2 (P = 7.75 x 10(-6)) whilst four were downregulated; ACVR1 (P = 9.01 x 10(-5)), NFATC2IP (P = 8.86 x 10(-5)), SUN1 (P = 3.87 x 10(-5)) and TTC9C (P = 7.18 x 10(-6)). These genes were also highly expressed in carotid atherosclerotic plaques. Conclusions We found seven genes involved in STEMI. The study is unique regarding the blood sampling in the acute phase and omission of secondary expressed genes from innate immunity. However, the results need to be replicated by future studies.
Subject headings and genre
Added entries (persons, corporate bodies, meetings, titles ...)
-
Lundman, P.Karolinska Institutet
(author)
-
Folkersen, L.
(author)
-
Paulsson-Berne, G.Karolinska Institutet
(author)
-
Karadimou, G.Karolinska Institutet
(author)
-
Eriksson, P.Karolinska Institutet
(author)
-
Caidahl, Kenneth,1949Karolinska Institutet,Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för molekylär och klinisk medicin,Institute of Medicine, Department of Molecular and Clinical Medicine(Swepub:gu)xcaike
(author)
-
Gabrielsen, A.Karolinska Institutet
(author)
-
Jernberg, T.Karolinska Institutet
(author)
-
Persson, J.Karolinska Institutet
(author)
-
Tornvall, P.Karolinska Institutet
(author)
-
Karolinska InstitutetInstitutionen för medicin, avdelningen för molekylär och klinisk medicin
(creator_code:org_t)
Related titles
-
In:Journal of Internal Medicine: Wiley287:1, s. 66-770954-68201365-2796
Internet link
Find in a library
To the university's database
- By the author/editor
-
Cederstrom, S.
-
Lundman, P.
-
Folkersen, L.
-
Paulsson-Berne, ...
-
Karadimou, G.
-
Eriksson, P.
-
show more...
-
Caidahl, Kenneth ...
-
Gabrielsen, A.
-
Jernberg, T.
-
Persson, J.
-
Tornvall, P.
-
show less...
- About the subject
-
- MEDICAL AND HEALTH SCIENCES
-
MEDICAL AND HEAL ...
-
and Clinical Medicin ...
- Articles in the publication
-
Journal of Inter ...
- By the university
-
University of Gothenburg
-
Karolinska Institutet