DNA methylation in the inflammatory genes after neurosurgery and diagnostic ability of post-operative delirium
The pathophysiological mechanisms of postoperative delirium (POD) are still not clear, and no reliable biomarker is available to differentiate those with and without POD. Pre- and post-surgery blood from epilepsy subjects undergoing neurosurgery were collected. DNA methylation (DNAm) levels of the T...
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Veröffentlicht in: | Translational psychiatry 2021-12, Vol.11 (1), p.627-627, Article 627 |
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Sprache: | eng |
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Zusammenfassung: | The pathophysiological mechanisms of postoperative delirium (POD) are still not clear, and no reliable biomarker is available to differentiate those with and without POD. Pre- and post-surgery blood from epilepsy subjects undergoing neurosurgery were collected. DNA methylation (DNAm) levels of the
TNF
gene,
IL1B
gene, and
IL6
gene by the Illumina EPIC array method, and DNAm levels of the
TNF
gene by pyrosequencing, were analyzed. Blood from 37 subjects were analyzed by the EPIC array method, and blood from 27 subjects were analyzed by pyrosequencing. Several CpGs in the
TNF
gene in preoperative blood showed a negative correlation between their DNAm and age both in the POD group and in the non-POD group. However, these negative correlations were observed only in the POD group after neurosurgery. Neurosurgery significantly altered DNAm levels at 17 out of 24 CpG sites on the
TNF
gene, 8 out of 14 CpG sites on the
IL1B
gene, and 4 out of 14 CpG sites on the
IL6
gene. Furthermore, it was found that the Inflammatory Methylation Index (IMI), which was based on the post-surgery DNAm levels at the selected five CpG sites, can be a potential detection tool for delirium with moderate accuracy; area under the curve (AUC) value was 0.84. The moderate accuracy of this IMI was replicated using another cohort from our previous study, in which the AUC was 0.79. Our findings provide further evidence of the potential role of epigenetics and inflammation in the pathophysiology of delirium. |
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ISSN: | 2158-3188 2158-3188 |
DOI: | 10.1038/s41398-021-01752-6 |