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Table 3 Overview over SNPs significantly associated with POD in CGAS approach

From: Association between genetic variants of the cholinergic system and postoperative delirium and cognitive dysfunction in elderly patients

Chr

SNP

Gene name

Position

OR [95% CI]

P-value

Adjusted P-value

7

rs8191992

CHRM2

137,016,561

0.61 [0.46; 0.80]

< 0.001

0.01

7

rs6962027

CHRM2

137,017,188

1.59 [1.22; 2.09]

< 0.001

0.01

11

rs2067482

CHRM4

46,385,217

1.64 [1.10; 2.44]

0.01

0.03

  1. Entered variables into logistic regression analysis: age (years), Charlson Comorbidity Index and duration of anesthesia. Data are expressed as odds ratio (OR) and 95% confidence interval (CI). OR refer to minor allele counts (0, 1, 2). P-values were adjusted for multiple testing by applying the Benjamini–Hochberg method according to the number of SNPs examined per cholinergic gene. Adjusted P ≤ 0.05 was considered as statistically significant
  2. Chr, Chromosome; SNP, single-nucleotide polymorphism