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. 2020 Oct 23;11:514136. doi: 10.3389/fneur.2020.514136

Table 3.

Number and percentages of the noADMCI-noEEA and noADMCI-EEA patients assuming the selective serotonin reuptake inhibitors (SSRIs), selective serotonin and noradrenaline reuptake inhibitors (SNRIs), benzodiazepines (BZDs), non-benzodiazepines GABA acting agent (No BZDs), and acetylcholinesterase inhibitors (AChEIs).

Drugs noADMCI-noEEA noADMCI-EEA Fisher test
N (%) N (%)
Selective serotonin reuptake inhibitors (SSRIs) 8 42.1 6 46.2 p = 0.9
Selective serotonin and noradrenaline reuptake inhibitors (SNRIs) 1 5.3 0 0 p = 0.9
Benzodiazepine (BZD) 4 21.2 3 23.1 p = 0.9
Non benzodiazepine GABA acting agent (No BZD) 1 5.3 0 0 p = 0.9
Acetylcholinesterase inhibitor (AChEI) 2 10.5 1 0 p = 0.9
All drugs 10 52.6 7 53.8 p = 0.9

The results of the presence or absence of statistically significant differences (Fisher test, p < 0.05 corrected) between the noADMCI-noEEA and noADMCI-EEA groups. The consumption of those drugs is also reported. All ADMCI patients had the information relative to the drug consumption available. noADMCI-noEEA, patients with mild cognitive impairment not due to Alzheimer's disease and without epileptiform EEG activity; noADMCI-EEA, patients with mild cognitive impairment not due to Alzheimer's disease and epileptiform EEG activity. No significant difference was observed between the two noADMCI groups even when a marginal threshold of p < 0.05 uncorrected was used.