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Study · Randomized controlled trial · n = 60 · 2024

9 results

Ingestion of β-nicotinamide mononucleotide increased blood NAD levels, maintained walking speed, and improved sleep quality in older adults in a double-blind randomized, placebo-controlled study.

Morifuji M, Higashi S, Ebihara S, Nagata M

GeroScience24 May 2024Cited by 20 (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 study9

9 results from studies that gave the peptide. 9 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In older adults, NMN did not significantly change stepping test performance versus placebo at either 4 or 12 weeks.

    In plain wordsIn older adults, stepping test performance did not differ significantly between NMN and placebo at 4 or 12 weeks.

    Outcome
    No significant changeStepping test at 4 and 12 weeks
    Study

    n = 60

    Comparator
    placebo
    Analysis
    Primary
    Outcome group
    Exercise and physical function · Musculoskeletal
    Studied dose
    250 mg/day · oral · 12 weeksAs given in this study (human).

    Source sentences

    Summary
    At primary outcome, at both 4 weeks and 12 weeks, the NMN and placebo groups had no significant differences in a stepping test.
    2 context sentences
    Summary · context
    In this randomized, placebo-controlled, double-blind, parallel-group comparison study, 60 participants were randomly allocated into a placebo group or NMN group.
    Summary · context
    Members of the NMN group consumed 250 mg/day NMN for 12 weeks.
  2. 02HumanRandomized controlled trialEfficacy outcome

    In older adults, NMN reduced 4-m walking time versus placebo after 12 weeks.

    In plain wordsIn older adults, NMN shortened walking time versus placebo after 12 weeks.

    Outcome
    Decrease4-m walking time
    Study

    n = 60

    Comparator
    placebo
    Analysis
    Secondary
    Outcome group
    Exercise and physical function · Musculoskeletal
    Studied dose
    250 mg/day · oral · 12 weeksAs given in this study (human).

    Source sentences

    Summary
    At secondary outcomes, after 12 weeks of NMN intake, the NMN group had a significantly shorter 4-m walking time than the placebo group as well as significantly higher blood levels of NAD + and its metabolites.
    2 context sentences
    Summary · context
    In this randomized, placebo-controlled, double-blind, parallel-group comparison study, 60 participants were randomly allocated into a placebo group or NMN group.
    Summary · context
    Members of the NMN group consumed 250 mg/day NMN for 12 weeks.
  3. 03HumanRandomized controlled trialEfficacy outcome

    In older adults, NMN increased blood NAD+ and its metabolites versus placebo after 12 weeks.

    In plain wordsIn older adults, NMN increased blood NAD+ and its metabolites versus placebo after 12 weeks.

    Outcome
    IncreaseBlood NAD+ and its metabolites
    Study

    n = 60

    Comparator
    placebo
    Analysis
    Secondary
    Outcome group
    Pharmacokinetics · Metabolic and weight
    Studied dose
    250 mg/day · oral · 12 weeksAs given in this study (human).

    Source sentences

    Summary
    At secondary outcomes, after 12 weeks of NMN intake, the NMN group had a significantly shorter 4-m walking time than the placebo group as well as significantly higher blood levels of NAD + and its metabolites.
    2 context sentences
    Summary · context
    In this randomized, placebo-controlled, double-blind, parallel-group comparison study, 60 participants were randomly allocated into a placebo group or NMN group.
    Summary · context
    Members of the NMN group consumed 250 mg/day NMN for 12 weeks.
  4. 04HumanRandomized controlled trialEfficacy outcome

    In older adults, NMN lowered daytime dysfunction scores versus placebo at 12 weeks.

    In plain wordsIn older adults, NMN reduced daytime dysfunction scores versus placebo at 12 weeks.

    Outcome
    DecreaseDaytime dysfunction score
    Study

    n = 60

    Comparator
    placebo
    Analysis
    Secondary
    Outcome group
    Sleep · Sleep
    Studied dose
    250 mg/day · oral · 12 weeksAs given in this study (human).

    Source sentences

    Summary
    The NMN group had improved sleep quality at 12 weeks relative to the placebo group as evidenced by lower scores for "Daytime dysfunction" and "Global PSQI" on the Pittsburgh Sleep Questionnaire.
    2 context sentences
    Summary · context
    In this randomized, placebo-controlled, double-blind, parallel-group comparison study, 60 participants were randomly allocated into a placebo group or NMN group.
    Summary · context
    Members of the NMN group consumed 250 mg/day NMN for 12 weeks.
  5. 05HumanRandomized controlled trialEfficacy outcome

    In older adults, NMN lowered Global PSQI scores versus placebo at 12 weeks.

    In plain wordsIn older adults, NMN improved overall sleep scores versus placebo at 12 weeks.

    Outcome
    DecreaseGlobal PSQI score
    Study

    n = 60

    Comparator
    placebo
    Analysis
    Secondary
    Outcome group
    Sleep · Sleep
    Studied dose
    250 mg/day · oral · 12 weeksAs given in this study (human).

    Source sentences

    Summary
    The NMN group had improved sleep quality at 12 weeks relative to the placebo group as evidenced by lower scores for "Daytime dysfunction" and "Global PSQI" on the Pittsburgh Sleep Questionnaire.
    2 context sentences
    Summary · context
    In this randomized, placebo-controlled, double-blind, parallel-group comparison study, 60 participants were randomly allocated into a placebo group or NMN group.
    Summary · context
    Members of the NMN group consumed 250 mg/day NMN for 12 weeks.
  6. 06HumanRandomized controlled trialSafety outcome

    In older adults, no adverse effects related to test substance consumption were observed.

    In plain wordsIn older adults, the study reported no adverse effects related to the test substance.

    Outcome
    Not applicableTreatment-related adverse effects
    Study

    n = 60

    Outcome group
    Adverse events · Whole body
    Studied dose
    250 mg/day · oral · 12 weeksAs given in this study (human).

    Source sentences

    Summary
    No adverse effects related to test substance consumption were observed.
    2 context sentences
    Summary · context
    In this randomized, placebo-controlled, double-blind, parallel-group comparison study, 60 participants were randomly allocated into a placebo group or NMN group.
    Summary · context
    Members of the NMN group consumed 250 mg/day NMN for 12 weeks.
  7. 07HumanRandomized controlled trialMechanism

    In older adults, changes in walking time correlated negatively with changes in blood NAD at 12 weeks.

    In plain wordsIn older adults, greater blood NAD increases were linked to shorter walking times at 12 weeks.

    Outcome
    DecreaseWalking time association with NAD change
    Study

    n: not reported in source

    Outcome group
    Exercise and physical function · Musculoskeletal
    Studied dose
    250 mg/day · oral · 12 weeksAs given in this study (human).

    Source sentences

    Summary
    A significant negative correlation was observed between the change in the 4-m walking time and the change in blood NAD + , N1-methyl-2-pridone-5-carboxamide (2-PY), and N1-methyl-4-pridone-3-carboxamide (4-PY) at 12 weeks.
    2 context sentences
    Summary · context
    In this randomized, placebo-controlled, double-blind, parallel-group comparison study, 60 participants were randomly allocated into a placebo group or NMN group.
    Summary · context
    Members of the NMN group consumed 250 mg/day NMN for 12 weeks.
  8. 08HumanRandomized controlled trialMechanism

    In older adults, changes in walking time correlated negatively with changes in blood 2-PY at 12 weeks.

    In plain wordsIn older adults, greater blood 2-PY increases were linked to shorter walking times at 12 weeks.

    Outcome
    DecreaseWalking time association with 2-PY change
    Study

    n: not reported in source

    Outcome group
    Exercise and physical function · Musculoskeletal
    Studied dose
    250 mg/day · oral · 12 weeksAs given in this study (human).

    Source sentences

    Summary
    A significant negative correlation was observed between the change in the 4-m walking time and the change in blood NAD + , N1-methyl-2-pridone-5-carboxamide (2-PY), and N1-methyl-4-pridone-3-carboxamide (4-PY) at 12 weeks.
    2 context sentences
    Summary · context
    In this randomized, placebo-controlled, double-blind, parallel-group comparison study, 60 participants were randomly allocated into a placebo group or NMN group.
    Summary · context
    Members of the NMN group consumed 250 mg/day NMN for 12 weeks.
  9. 09HumanRandomized controlled trialMechanism

    In older adults, changes in walking time correlated negatively with changes in blood 4-PY at 12 weeks.

    In plain wordsIn older adults, greater blood 4-PY increases were linked to shorter walking times at 12 weeks.

    Outcome
    DecreaseWalking time association with 4-PY change
    Study

    n: not reported in source

    Outcome group
    Exercise and physical function · Musculoskeletal
    Studied dose
    250 mg/day · oral · 12 weeksAs given in this study (human).

    Source sentences

    Summary
    A significant negative correlation was observed between the change in the 4-m walking time and the change in blood NAD + , N1-methyl-2-pridone-5-carboxamide (2-PY), and N1-methyl-4-pridone-3-carboxamide (4-PY) at 12 weeks.
    2 context sentences
    Summary · context
    In this randomized, placebo-controlled, double-blind, parallel-group comparison study, 60 participants were randomly allocated into a placebo group or NMN group.
    Summary · context
    Members of the NMN group consumed 250 mg/day NMN for 12 weeks.

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

    21 Oct 2026, 15:58 UTC

    Study results updated

  2. Version 1

    21 Oct 2026, 12:50 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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