Skip to content

Study · Non-randomized trial · n = 67 · 2018

5 results

[Prevention of progression of cognitive decline in the first-degree relatives of patients with Alzheimer's disease].

Selezneva ND, Roshchina IF, Korovaitseva GI, Gavrilova SI

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova1 Jan 2018Cited by 1 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study5

5 results from studies that gave the peptide. 5 results from people.

  1. 01HumanNon-randomized trialEfficacy outcome

    In first-degree relatives of Alzheimer's disease patients, a positive CGI effect was reported in 77.6% after Cerebrolysin treatment.

    In plain wordsIn relatives of Alzheimer's disease patients, 77.6% showed a positive clinical impression score response after Cerebrolysin treatment.

    Outcome
    IncreaseCGI positive response
    Study

    n = 67

    Outcome group
    Cognition and memory · Nervous system and cognition
    Studied dose
    20 ml/day · intravenous · 1 monthAs given in this study (human).

    Measurements

    Positive CGI effect
    77.6%
    Relatives

    Source sentences

    Summary
    The positive effect of course treatment on the CGI was established in 77.6% of the relatives.
    2 context sentences
    Summary · context
    Sixty-seven relatives (mean age 57.6±14.2 y.o.) received cerebrolysin in the dose of 20 ml/day in intravenous drips in 100 ml isotonic saline.
    Summary · context
    The duration of treatment was 1 month.
  2. 02HumanNon-randomized trialEfficacy outcome

    In relatives without cognitive difficulties, MMSE scores significantly improved after Cerebrolysin treatment.

    In plain wordsIn relatives without cognitive difficulties, MMSE scores improved after Cerebrolysin treatment.

    Outcome
    IncreaseMMSE score without cognitive difficulties
    Study

    n = 40

    Outcome group
    Cognition and memory · Nervous system and cognition
    Studied dose
    20 ml/day · intravenous · 1 monthAs given in this study (human).

    Source sentences

    Summary
    The scores on the MMSE and MoCA scales were significantly improved in the group with cognitive difficulties objectively confirmed by the clinical/neuropsychological examination (n=27) and in the group without cognitive difficulties (n=40).
    2 context sentences
    Summary · context
    Sixty-seven relatives (mean age 57.6±14.2 y.o.) received cerebrolysin in the dose of 20 ml/day in intravenous drips in 100 ml isotonic saline.
    Summary · context
    The duration of treatment was 1 month.
  3. 03HumanNon-randomized trialEfficacy outcome

    In relatives without cognitive difficulties, MoCA scores significantly improved after Cerebrolysin treatment.

    In plain wordsIn relatives without cognitive difficulties, MoCA scores improved after Cerebrolysin treatment.

    Outcome
    IncreaseMoCA score without cognitive difficulties
    Study

    n = 40

    Outcome group
    Cognition and memory · Nervous system and cognition
    Studied dose
    20 ml/day · intravenous · 1 monthAs given in this study (human).

    Source sentences

    Summary
    The scores on the MMSE and MoCA scales were significantly improved in the group with cognitive difficulties objectively confirmed by the clinical/neuropsychological examination (n=27) and in the group without cognitive difficulties (n=40).
    2 context sentences
    Summary · context
    Sixty-seven relatives (mean age 57.6±14.2 y.o.) received cerebrolysin in the dose of 20 ml/day in intravenous drips in 100 ml isotonic saline.
    Summary · context
    The duration of treatment was 1 month.
  4. 04HumanNon-randomized trialEfficacy outcome

    In relatives with confirmed cognitive difficulties, MMSE scores significantly improved after Cerebrolysin treatment.

    In plain wordsIn relatives with confirmed cognitive difficulties, MMSE scores improved after Cerebrolysin treatment.

    Outcome
    IncreaseMMSE score with confirmed cognitive difficulties
    Study

    n = 27

    Outcome group
    Cognition and memory · Nervous system and cognition
    Studied dose
    20 ml/day · intravenous · 1 monthAs given in this study (human).

    Source sentences

    Summary
    The scores on the MMSE and MoCA scales were significantly improved in the group with cognitive difficulties objectively confirmed by the clinical/neuropsychological examination (n=27) and in the group without cognitive difficulties (n=40).
    2 context sentences
    Summary · context
    Sixty-seven relatives (mean age 57.6±14.2 y.o.) received cerebrolysin in the dose of 20 ml/day in intravenous drips in 100 ml isotonic saline.
    Summary · context
    The duration of treatment was 1 month.
  5. 05HumanNon-randomized trialEfficacy outcome

    In relatives with confirmed cognitive difficulties, MoCA scores significantly improved after Cerebrolysin treatment.

    In plain wordsIn relatives with confirmed cognitive difficulties, MoCA scores improved after Cerebrolysin treatment.

    Outcome
    IncreaseMoCA score with confirmed cognitive difficulties
    Study

    n = 27

    Outcome group
    Cognition and memory · Nervous system and cognition
    Studied dose
    20 ml/day · intravenous · 1 monthAs given in this study (human).

    Source sentences

    Summary
    The scores on the MMSE and MoCA scales were significantly improved in the group with cognitive difficulties objectively confirmed by the clinical/neuropsychological examination (n=27) and in the group without cognitive difficulties (n=40).
    2 context sentences
    Summary · context
    Sixty-seven relatives (mean age 57.6±14.2 y.o.) received cerebrolysin in the dose of 20 ml/day in intravenous drips in 100 ml isotonic saline.
    Summary · context
    The duration of treatment was 1 month.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    14 Oct 2026, 05:02 UTC

    Study results updated

  2. Version 1

    14 Oct 2026, 01:46 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

PepBank is a research reference. Talk to a doctor before you use any peptide.