# Berry Consumption and Its Role in the Modulation of Obesity and Mild Cognitive Impairment

**Authors:** Gustavo Alves Andrade dos Santos, Caroline Pereira Mourão Moraes, Mário Roberto Maróstica Júnior

PMC · DOI: 10.3390/nu18040674 · Nutrients · 2026-02-19

## TL;DR

This paper reviews how eating berries may help reduce obesity and protect brain health, potentially lowering the risk of mild cognitive impairment and dementia.

## Contribution

The paper systematically reviews human studies on the effects of red fruit consumption on obesity and cognitive decline, focusing on neurodegenerative biomarkers.

## Key findings

- Berry-derived compounds may improve memory and reduce TAU protein and β-amyloid accumulation.
- Limited evidence suggests berries may support metabolic health and insulin sensitivity.
- Few human trials exist, and findings remain inconclusive for broader neuroprotective effects.

## Abstract

Most dementias are preceded by mild cognitive impairment (MCI), a transitional clinical stage characterized by cognitive decline that does not yet significantly interfere with activities of daily living. Obesity and diabetes are among the major risk factors for MCI and are strongly associated with unhealthy lifestyle patterns. The growing global prevalence of obesity has intensified the need for effective dietary strategies that promote both weight control and neuroprotection. Red fruits, which are rich in bioactive compounds such as anthocyanins, have demonstrated potential roles in modulating metabolic pathways and cognitive function. This systematic review aimed to identify and synthesize evidence from human studies published over the past two decades that examined the effects of red fruit consumption on obesity-related mechanisms and cognitive outcomes, as well as its influence on key neurodegenerative biomarkers, including TAU protein, β-amyloid, and neurofilament light chain. A systematic search was conducted in major scientific databases to identify human clinical trials evaluating the metabolic and neuroprotective effects of berry-derived compounds. Eligible studies were screened for outcomes related to cognitive performance, obesity-related parameters, and relevant molecular biomarkers. The included studies reported modest improvements in cognitive domains, with the most consistent effects observed in memory-related outcomes. Berry-derived bioactive compounds demonstrated potential in attenuating TAU protein hyperphosphorylation and reducing β-amyloid accumulation; however, the available evidence remains limited and requires further confirmation. Human clinical studies remain scarce, and although some trials reported favorable metabolic effects, these findings are still inconclusive. Reported outcomes included improvements in insulin sensitivity, regulation of leptin levels, and modulation of the gut–brain axis, which may collectively contribute to a reduced risk of obesity. Based on the studies evaluated in this review, there remains a limited number of human clinical trials that robustly support the neuroprotective and complementary metabolic effects of berry-derived bioactive compounds. Nevertheless, the available evidence suggests that dietary strategies incorporating wild fruits rich in polyphenols may represent a promising complementary approach for the prevention of mild cognitive impairment (MCI) and obesity, with potential implications for reducing the risk of dementia progression.

## Linked entities

- **Chemicals:** anthocyanins (PubChem CID 145858)
- **Diseases:** obesity (MONDO:0011122), diabetes (MONDO:0005015), dementia (MONDO:0001627)

## Full-text entities

- **Genes:** SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, CREB1 (cAMP responsive element binding protein 1) [NCBI Gene 1385] {aka CREB, CREB-1}, NGF (nerve growth factor) [NCBI Gene 4803] {aka Beta-NGF, HSAN5, NGFB}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, CAT (catalase) [NCBI Gene 847], VCAM1 (vascular cell adhesion molecule 1) [NCBI Gene 7412] {aka CD106, INCAM-100}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, Foxo1 (forkhead box O1) [NCBI Gene 56458] {aka Afxh, FKHR, Fkhr1, Foxo1a}, GFAP (glial fibrillary acidic protein) [NCBI Gene 2670] {aka ALXDRD}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, Iars1 (isoleucyl-tRNA synthetase 1) [NCBI Gene 105148] {aka 2510016L12Rik, E430001P04Rik, ILRS, Iars}, NAMPT (nicotinamide phosphoribosyltransferase) [NCBI Gene 10135] {aka 1110035O14Rik, PBEF, PBEF1, VF, VISFATIN}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, Insr (insulin receptor) [NCBI Gene 16337] {aka 4932439J01Rik, CD220, D630014A15Rik, IR, IR-A, IR-B}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, MAPK8 (mitogen-activated protein kinase 8) [NCBI Gene 5599] {aka JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8}, NOX4 (NADPH oxidase 4) [NCBI Gene 50507] {aka KOX, KOX-1, RENOX}, RETN (resistin) [NCBI Gene 56729] {aka ADSF, FIZZ3, RENT, RETN1, RSTN, XCP1}, ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 9370] {aka ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1}, PTK2B (protein tyrosine kinase 2 beta) [NCBI Gene 2185] {aka CADTK, CAKB, FADK2, FAK2, PKB, PTK}, DNMT1 (DNA methyltransferase 1) [NCBI Gene 1786] {aka ADCADN, AIM, CXXC9, DNMT, HSN1E, MCMT}, Gsk3b (glycogen synthase kinase 3 beta) [NCBI Gene 56637] {aka 7330414F15Rik, 8430431H08Rik, GSK-3, GSK-3beta, GSK3}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, NEFL (neurofilament light chain) [NCBI Gene 4747] {aka CMT1F, CMT2E, CMTDIG, NF-L, NF68, NFL}, ICAM1 (intercellular adhesion molecule 1) [NCBI Gene 3383] {aka BB2, CD54, P3.58}, BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}, HMOX1 (heme oxygenase 1) [NCBI Gene 3162] {aka HMOX1D, HO-1, HSP32, bK286B10}, JUNB (JunB proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 3726] {aka AP-1}, CFD (complement factor D) [NCBI Gene 1675] {aka ADIPSIN, ADN, DF, PFD}, Akt1 (Akt serine/threonine kinase 1) [NCBI Gene 11651] {aka Akt, LTR-akt, PKB, PKB/Akt, PKBalpha, Rac}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}
- **Diseases:** Lewy bodies (MESH:D020961), neuroinflammation (MESH:D000090862), food allergies (MESH:D005512), insulin resistance (MESH:D007333), anxiety (MESH:D001007), vascular dysfunction (MESH:D002561), prediabetes (MESH:D011236), weight loss (MESH:D015431), cardiovascular, respiratory, renal, gastrointestinal, or neurological disorders (MESH:D005767), diabetes (MESH:D003920), hypertrophy (MESH:D006984), Dysbiosis (MESH:D064806), attention and memory difficulties (MESH:D001289), cancer (MESH:D009369), AD (MESH:D000544), MCI (MESH:D060825), Mental Disorders (MESH:D001523), brain atrophy (MESH:C566985), cardiovascular complications (MESH:D002318), neurotoxicity (MESH:D020258), PD (MESH:D010300), colon cancer (MESH:D015179), mitochondrial dysfunction (MESH:D028361), brain injury (MESH:D001930), deaths (MESH:D003643), visual, auditory, or language impairments (MESH:D014786), cardiometabolic disease (MESH:D024821), injury to (MESH:D014947), neurodegeneration (MESH:D019636), excess (MESH:D006970), Central nervous system inflammation (MESH:D007249), chronic (MESH:D002908), neurofibrillary (MESH:D055956), Memory (MESH:D008569), Damage to Cognitive Functions (MESH:D003072), synaptic dysfunction (MESH:C536122), metabolic dysregulation (MESH:D021081), neurological disorders (MESH:D009461), Major Neurocognitive Disorder (MESH:D003865), metabolic (MESH:D008659), MS (MESH:D009103), overweight (MESH:D050177), systemic (MESH:D015619), amyloid (MESH:C000718787), Dementia (MESH:D003704), stroke (MESH:D020521), carcinogenesis (MESH:D063646), infarcts (MESH:D007238), depressive symptoms (MESH:D003866), DIO (MESH:D009765), adiposity (MESH:D018205), neuronal injury (MESH:D009410), type 2 diabetes (MESH:D003924), cerebral amyloid (MESH:D016657), mood disorders (MESH:D019964), weight gain (MESH:D015430)
- **Chemicals:** tocopherols (MESH:D024505), flavonols (MESH:D044948), Triglyceride (MESH:D014280), phenylalanine (MESH:D010649), stilbenes (MESH:D013267), tannins (MESH:D013634), flavanones (MESH:D044950), Quercetin (MESH:D011794), lignans (MESH:D017705), omega-3 fatty acids (MESH:D015525), aromatic amino acids (MESH:D024322), sugars (MESH:D000073893), curcumin (MESH:D003474), flavan-3-ols (MESH:C404987), MJP (-), fat (MESH:D005223), blood glucose (MESH:D001786), SCFAs (MESH:D005232), ROS (MESH:D017382), chlorogenic acid (MESH:D002726), glucose (MESH:D005947), cyanidin-3-O-glucoside (MESH:C462279), serotonin (MESH:D012701), Flavonoid (MESH:D005419), cholesterol (MESH:D002784), alcohol (MESH:D000438), ellagic acid (MESH:D004610), vitamin C. (MESH:D001205), tryptophan (MESH:D014364), ACN (MESH:D000872), glutamate (MESH:D018698), norepinephrine (MESH:D009638), GABA (MESH:D005680), dopamine (MESH:D004298), flavones (MESH:D047309), EC (MESH:D002392), streptozotocin (MESH:D013311), free fatty acids (MESH:D005230), LPSs (MESH:D008070), stearic acid (MESH:C031183), lipid (MESH:D008055), phenolic acids (MESH:C017616), carotenoids (MESH:D002338), SB (MESH:D000965), Polyphenols (MESH:D059808), tyrosine (MESH:D014443), Curcuminoids (MESH:D036381)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Glycine max (soybean, species) [taxon 3847], Akkermansia muciniphila (species) [taxon 239935], gut metagenome (species) [taxon 749906], Rubus occidentalis (black raspberry, species) [taxon 75079]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12943443/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943443/full.md

## References

116 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943443/full.md

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Source: https://tomesphere.com/paper/PMC12943443