Table 1. Characteristics of included systematic reviews.
| Reference | Population criteria & age | Intervention | Comparison | Outcome | Quality of the Evidence (grade) |
|---|---|---|---|---|---|
| Wang et al. 11 | 40 male participants.Range of age: 18–30 years.Mean age of participants: 20.2 years intervention, 21.5 years control. | L-Carnitine. | Placebo | No significant improvement in relevant indicators for DS patients. | Overall Neurological Efficacy: Low (due to inconsistency and imprecision). |
| Livingstone et al. 12 | Down’s Syndrome (DS) participants aged 18 and above. 427 participants. | Memantine, Simvastatin, Donepezil, Antioxidant, Acetyl-L-carnitine. | Placebo | Overall insufficient evidence to confirm effectiveness. | Cognitive Efficacy: Low (due to inconsistency and imprecision). |
| Oliveira e Faria 14 | Adults with DS with signs of dementia. 626 participants. | Antioxidant, acetylcholinesterase inhibitor (donepezil), NMDA receptor antagonists (memantine), fast-acting intranasal insulin. | Placebo. | The use of pharmacological therapies did not demonstrate relevant effects in the treatment of dementia. | Cognitive Efficacy: Low (due to inconsistency and imprecision). |
| Corniello et al. 15 | 46 patients with DS, men and women.Progressive cognitive decline, Diagnosis of Alzheimer’s disease (AD) in all cases. | Levetiracetam (LEV) monotherapy, valproic acid (VPA) monotherapy and other anticonvulsants polytherapy. | No placebo group/usual care defined. | LEV and VPA showed great efficacy in seizure control. Treatment with LEV may enhance memory deficits, leading to amelioration of cognitive performances. | Evidence Certainty: Low (due to risk of bias, inconsistency and imprecision) |
| Islam et al. 13 | Down’s Syndrome (DS) participants aged 15 and above. 168 participants. | Memantine | Placebo | No significant effect on the outcomes of cognitive function. | Cognitive Efficacy: Low (due to risk of bias and imprecision) |