Effect of matcha green tea on cognitive functions and sleep quality in older adults with cognitive decline: A randomized controlled study over 12 months.

Kazuhiko Uchida, Kohji Meno, Tatsumi Korenaga, Shan Liu, Hideaki Suzuki, Yoshitake Baba, Chika Tagata, Yoshiharu Araki, Shuto Tsunemi, Kenta Aso, Shun Inagaki, Sae Nakagawa, Makoto Kobayashi, Tatsuyuki Kakuma, Takashi Asada, Miho Ota, Takanobu Takihara, Tetsuaki Arai

Journal: PloS one 2024;19(8):e0309287

PMID: 39213264

Plain Language Summary

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Accumulating evidence suggests that lifestyle habits after middle age (approximately 45–54 years old) significantly impact the maintenance of cognitive function in older adults. Tea consumption, including matcha green tea, is closely linked to these habits. Matcha contains bioactive compounds such as epigallocatechin gallate (EGCG), theanine, and caffeine, which have known benefits for cognitive function and mood. This study aimed to assess the effects of matcha on sleep quality and cognitive decline in older adults. This study was a 12-month randomised, double-blind, placebo-controlled trial enrolling 99 community-dwelling older adults (aged 60–85 years) with mild cognitive impairment or subjective cognitive decline. Participants consumed either nine capsules of matcha (equivalent to 2 g) or placebo daily. Results showed that matcha consumption improved specific cognitive functions, including facial expression recognition and attention, and enhanced sleep quality, as indicated by improvements in the Pittsburgh Sleep Quality Index (PSQI) scores. A significant enhancement in social cognition was also observed in the matcha group. Authors concluded that regular matcha intake may help improve emotional perception and sleep quality in older adults with cognitive decline.

Expert Review

Reviewer: Wilma Kirsten
14th Mar 2025
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Conflict of interest

None

Take home message

  • Dementia pathophysiology is believed to develop in middle age (approximately 45–54 years-old). Nutritional support that focuses on maintenance of cognitive function should therefore be considered when presented with a patient in this age range even when no cognitive impairment symptomatology presents.
  • Sleep support is fundamental given its association with cognitive decline; early intervention and maintenance of good sleep patterns are therefore crucial at any age.
  • Signs of facial emotion recognition impairment might be indicative of early stage mild cognitive impairment (MCI) and subjective cognitive decline (SCD). Nutritional support in terms of anti-inflammatory and anti-oxidant nutrients should therefore be part of an intervention dietary strategy in patients presenting with these symptoms.

Evidence category

A: Meta-analyses, position-stands, randomized-controlled trials (RCTs)

Summary review

Introduction

Aged-related dementia is a growing global concern with the number of affected patients projected to increase from 57.4 million in 2019 to 152.8 million by 2050. Disease progression is insidious and gradual and, as of yet, no effective treatment or indeed conclusive preventative strategy has been identified. Specific nutritional components of matcha green tea are believed to benefit cognitive function by means of antioxidant and anti-inflammatory properties.

Methods

A 12-month randomised, double-blind, placebo-controlled clinical trial assessed the potential of matcha in improving sleep quality and delaying cognitive decline in 99 community-dwelling older adults aged 60–85 years (89 patients completed the trial). Age, sex, and APOE genotype were adjusted for. The participants (n=49) consumed nine capsules of matcha (equivalent to 2 g of matcha) or placebo (n=50) daily at any time. Data collection included standardised cognitive function tests, Pittsburgh sleep quality index scores (PSQI), PET scans for 24 participants (9 male and 15 female), serum, and immunoassay of plasma Aβ1–40 and Aβ1–42 levels.

Results

There were no differences in baseline scores between the two cohorts. After 12-months of intervention a difference of 0.86 (95% CI; -0.002, 1.71) (P = 0.088) in PSQI scores were observed indicating an improvement in sleep quality for the matcha cohort. Significant improvements in social acuity in the neurocognitive domain was furthermore observed (difference; -1.39, 95%CI; -2.78, 0.002) (P = 0.028). There were no observable differences between the cohorts for the other cognitive tests or PET scans.

Conclusion

Even though matcha consumption has no direct impact on the development of dementia, the authors indicate it is a plausible lifestyle improvement strategy that has the potential to improve sleep quality and social acuity that are believed to play a role in the development of late-onset dementia.

Clinical practice applications

  • Matcha green tea powder contains epigallocatechin gallate (anti-oxidant and anti-inflammatory polyphenols) and theanine, an amino acid that is believed to alleviate stress and improve sleep quality.
  • The daily intake quantity of matcha was set at 2 g in this study because the amount of matcha in the traditional Japanese tea ceremony, Tea Otemae, is 2 g.
  • Matcha tea is therefore an affordable and easily implemented nutritional strategy to improve sleep quality and enhance social perception by providing specific dietary micronutrients for adults of any age.

Considerations for future research

  • Larger scale studies targeted at a more diverse cultural cohort are needed to support the outcome of this study.
  • Matcha tea is part of Japanese culture and the efficacy of intake in other cultures are needed to establish quantity reference guidelines.
  • The specific effects of matcha tea intake on dementia and Alzheimer biomarkers need further investigation.
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Abstract

OBJECTIVE

Lifestyle habits after middle age significantly impact the maintenance of cognitive function in older adults. Nutritional intake is closely related to lifestyle habits; therefore, nutrition is a pivotal factor in the prevention of dementia in the preclinical stages. Matcha green tea powder (matcha), which contains epigallocatechin gallate, theanine, and caffeine, has beneficial effects on cognitive function and mood. We conducted a randomized, double-blind, placebo-controlled clinical study over 12 months to examine the effect of matcha on cognitive function and sleep quality.

METHODS

Ninety-nine participants, including 64 with subjective cognitive decline and 35 with mild cognitive impairment were randomized, with 49 receiving 2 g of matcha and 50 receiving a placebo daily. Participants were stratified based on two factors: age at baseline and APOE genotype. Changes in cognitive function and sleep quality were analyzed using a mixed-effects model.

RESULTS

Matcha consumption led to significant improvements in social acuity score (difference; -1.39, 95% confidence interval; -2.78, 0.002) (P = 0.028) as evaluated by the perception of facial emotions in cognitive function. The primary outcomes, that is, Montreal Cognitive Assessment and Alzheimer's Disease Cooperative Study Activity of Daily Living scores, showed no significant changes with matcha intervention. Meanwhile, Pittsburgh Sleep Quality Index scores indicated a trend toward improvement with a difference of 0.86 (95% confidence interval; -0.002, 1.71) (P = 0.088) between the groups in changes from baseline to 12 months.

CONCLUSIONS

The present study suggests regular consumption of matcha could improve emotional perception and sleep quality in older adults with mild cognitive decline. Given the widespread availability and cultural acceptance of matcha green tea, incorporating it into the daily routine may offer a simple yet effective strategy for cognitive enhancement and dementia prevention.

Copyright: © 2024 Uchida et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Address: Institute of Biomedical Research, MCBI Inc., Tsukuba, Ibaraki, Japan.; Research Division, MCBI Inc., Tsukuba, Ibaraki, Japan.; Research Division, MCBI Inc., Tsukuba, Ibaraki, Japan.; Central Research Institute, ITO EN, LTD., Makinohara, Shizuoka, Japan.; Biostatistics Center, Kurume University Graduate School of Medicine, Kurume, Japan.; Memory Clinic Toride, Toride, Ibaraki, Japan.; Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.; Institute of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan.
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