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. 2022 Sep 20;16:998224. doi: 10.3389/fnins.2022.998224

Table 7.

Short-term response.

Reference Population Treatment Diagnosis Response criteria Follow-up Predictor Risk of bias
Boccardi et al. (2017) 628 AD patients Donepezil, galantamine, rivastigmine Not stated MMSE stabilization or improvement at 3 months 3 years Short-term response is not a predictor Moderate
Droogsma et al. (2015) 335 AD patients Donepezil, galantamine, rivastigmine (memantine) Clinical (NINCS-ADRDA, not stated if probable or possible) Change in MMSE (no deterioration in MMSe as initial response) Up to 10 years Initial response after 6 months is not a predictor of subsequent long-term response High
Mossello et al. (2004) 212 AD patients Donepezil, galantamine, rivastigmine Clinical (probable AD, NINCDS-ADRDA) No deterioration in MMSE at 3 months; not clearly stated, but change in MMSE, ADL, and IADL at 9 months 9 months No deterioration on MMSE after 3 months of therapy High
Raschetti et al. (2005) 5642 AD patients (2,853 completed the study) Donepezil, galantamine, rivastigmine Clinical (probable AD, NINCDS-ADRDA) 2+ points improvement on MMSE 9 months Absence of concomitant diseases and response at 3 months Moderate
Miranda et al. (2015) 129 AD and AD+CVD patients (97 completed the study) Donepezil, galantamine, rivastigmine Clinical (probable AD, NIAA, Ballinger et al., 2017; AD+CVD, NINDS-AIREN) Improvement of 2+ points on MMSE 12 months Being a very good responder at 3 and 6 months Moderate
Calabria et al. (2009) 427 AD patients (226 patients completed the study) Donepezil, rivastigmine Clinical (probable AD, NINCDS-ADRDA) Based on the distribution of MMSE change between baseline and follow-up: above 75th percentile very good responders, 50–70th good responders, 25–50th bad responders, under 25th very bad responders 21 months Greater improvement at 3 months High
Rota et al. (2007) 203 AD patients Donepezil, galantamine, rivastigmine Clinical (probable AD, NINCDS-ADRDA) Change in MMSE and BADL-IADL 30 months Higher MMSE (only for MMSE >18), BADL and IADL improvement at 3 months, all for response at 9 months Moderate
Horikoshi et al. (2020) 110 AD patients Donepezil, galantamine, rivastigmine, memantine Clinical (ICD-10) Change in MMSE the same or lower of lower confidence interval of mean change in MMSE (Rey et al., 2018) without treatment at 6 months; mean change in MMSE from baseline to 12 and 24 months 24 months Same or lower change in MMSE than lower confidence interval of mean change in MMSE without treatment at 6 months Moderate
Wattmo et al. (2018) 881 AD patients Donepezil, galantamine, rivastigmine Clinical (possible or probable AD, NINCDS-ADRDA, and DSM-IV) Institutionalization: permanent entry to a licensed skilled-nursing facility with 24-h care (not clearly defined as a response); improvement in MMSE, CIBIC (1–3), IADL, or PSMS at 6 months (but used as predictors) 3 years Improvement or no deterioration in a combination of MMSE, CIBIC, IADL and PSMS at 6 months are a predictor of delayed institutionalization High
Farlow et al. (2015) 716 severe AD patients (628 included) Rivastigmine 13.3 or 4.6 mg Clinical (probable AD, NINCDS-ADRDA) Improvement/improvement or no change on ADCS-CGIC 24 weeks Minimal worsening, no change or improvement on ADCS-CGIC at week 8 and 16 Some concerns—Low
Ohnishi et al. (2014) 303 AD patients Galantamine Clinical (probable AD, NINCDS-ADRDA) 4+ points improvement on ADAS-Cog Japanese version 24 weeks Improvement on word recognition by at least −1.5 points on ADAS-Cog after 4 weeks of treatment Some concerns—Low
Palmqvist et al. (2010) 75 AD patients Donepezil, galantamine, rivastigmine Clinical (probable or possible AD, NINCDS-ADRDA, see Borroni and Barrantes, 2021) 16 s impovement on A Quick Test—color form at 8 weeks or 3+ points improvement on MMSE at 8 weeks; change in AQT at 6 months 32 ± 19 months 16 s + improvement on AQT (A Quick Test—color form) after 8 weeks Moderate