Frontiers in Nutrition

Verbal memory gains in healthy Japanese adults 40+ with low scores

In a randomized trial, standardized verbal memory scores were 10.1 points higher with a scallop-derived supplement than with placebo after 12 weeks.

Paper by Mina Fukuchi, Mizuho Tanaka, Masafumi Nagata, Tsuyoshi Takara, Yasuhiro Sasuga · Hachioji Center for Research and Development
Figure 1. Flow diagram of participant recruitment, allocation, follow-up, and analysis.
Open the figure at full size
Figure 1. Flow diagram of participant recruitment, allocation, follow-up, and analysis.Flow diagram of participant recruitment, allocation, follow-up, and analysis.Fukuchi et al.
Randomized trial in 66 healthy Japanese adults with below-average verbal memory, against placeboInterventions

68 eligible participants, 12 weeks, double-blind, placebo-controlled, registered UMIN000057985

Limit: Repeated Cognitrax testing could raise scores through familiarity with the test

Stake: An author holds shares in B&S Corporation. An author works for ORTHOMEDICO.

Edited by Boris Djordjevic · AgingResearch.News

Follow

Researchers randomly assigned 68 cognitively healthy Japanese men and women aged 40 or older with below-average verbal memory for their age to a scallop-derived supplement or placebo. The double-blind trial tested 1 milligram daily of plasmalogens, fat molecules enriched in the brain, for 12 weeks.

The analysis included 66 participants, 33 in each group. On a web-based cognitive test, standardized verbal memory scores were 10.1 points higher with the supplement than with placebo after adjustment for baseline scores. Exploratory analyses also suggested improvements in selected attention measures. No adverse events were reported in either group, and assessments found no clinically meaningful safety concerns.

Why it matters

The trial addressed whether a dietary supplement might support cognitive function in otherwise healthy people in middle and later life.

Caveats

The analysis excluded two randomized participants who never received their assigned capsules, and follow-up lasted only 12 weeks. The findings do not cover adults under 40 or people with dementia or other disorders affecting cognition, and do not establish long-term safety.

From the paper

Participants

Of the 168 individuals who provided informed consent, 68 met the eligibility criteria and were randomly assigned to the sPls or placebo group.

Methods, Selection, randomization, and blinding

Who took part

Inclusion criteria were healthy Japanese adults, both sexes, aged ≥40 years with verbal memory performance below the age-matched normative mean, absence of clinically diagnosed disease, a MMSE-J score of at least 24 at screening and a validity index of “yes” on the Cognitrax verbal memory test with a standardized verbal memory score <100 at screening …

Methods, Participants

Duration

Efficacy and safety were assessed at baseline and after 12 weeks of intervention.

Methods, Study design and ethical approval

Analyzed for verbal memory

As a result, 66 participants (33 per group) were included in both efficacy and safety analyses based on FAS.

Results, Participant disposition and baseline

Primary outcome

The EMMs were 89.4 ± 3.5 (SE) in the placebo group and 99.5 ± 3.5 in the sPls group, corresponding to a between-group difference of 10.1 (95% CI, 0.4–19.9; p = 0.042).

Results, Primary outcome

Harms

No adverse events were reported in either group.

Results, Safety evaluation

Limitation

Although the randomized, double-blind, placebo-controlled design strengthens the internal validity of the study, the sample size was primarily calculated based on the primary outcome.

Discussion

Attention

The EMM for complex attention was 101.1 ± 1.7 in the placebo group and 106.5 ± 1.7 in the sPls group (difference, 5.4; 95% CI, 0.6–10.3; p = 0.028).

Results, Secondary outcomes

Quoted word for word from the full text on PubMed Central.