Evidence map›Paper›PMID 33071750›Full record

ReviewFrontiers in neuroscience2020

The Potential Roles of Ghrelin in Metabolic Syndrome and Secondary Symptoms of Alzheimer's Disease.

Sujin Kim, Yunkwon Nam, Soo Jung Shin, Yong Ho Park, Seong Gak Jeon, Jin-Il Kim, Min-Jeong Kim, Minho Moon

Abstract readReview
In one paragraph

Review in Frontiers in neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Ghrelin system in Alzheimer's disease.Current opinion in neurobiology · 2023
    Review
  6. Phoenixin: More than Reproductive Peptide.International journal of molecular sciences · 2020
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Sujin KimDepartment of Biochemistry, College of Medicine, Konyang University, Daejeon, South Korea.
Yunkwon NamDepartment of Biochemistry, College of Medicine, Konyang University, Daejeon, South Korea.
Soo Jung ShinDepartment of Biochemistry, College of Medicine, Konyang University, Daejeon, South Korea.
Yong Ho ParkDepartment of Biochemistry, College of Medicine, Konyang University, Daejeon, South Korea.
Seong Gak JeonDepartment of Biochemistry, College of Medicine, Konyang University, Daejeon, South Korea.
Jin-Il KimDepartment of Nursing, College of Nursing, Jeju National University, Jeju-si, South Korea.
Min-Jeong KimDepartment of Biochemistry, College of Medicine, Konyang University, Daejeon, South Korea.
Minho MoonDepartment of Biochemistry, College of Medicine, Konyang University, Daejeon, South Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although the major causative factors of Alzheimer's disease (AD) are the accumulation of amyloid β and hyperphosphorylated tau, AD can also be caused by metabolic dysfunction. The major clinical symptom of AD is cognitive dysfunction. However, AD is also accompanied by various secondary symptoms such as depression, sleep-wake disturbances, and abnormal eating behaviors. Interestingly, the orexigenic hormone ghrelin has been suggested to have beneficial effects on AD-related metabolic syndrome and secondary symptoms. Ghrelin improves lipid distribution and alters insulin sensitivity, effects that are hypothesized to delay the progression of AD. Furthermore, ghrelin can relieve depression by enhancing the secretion of hormones such as serotonin, noradrenaline, and orexin. Moreover, ghrelin can upregulate the expression of neurotrophic factors such as brain-derived neurotrophic factor and modulate the release of proinflammatory cytokines such as tumor necrosis factor α and interleukin 1β. Ghrelin alleviates sleep-wake disturbances by increasing the levels of melatonin, melanin-concentrating hormone. Ghrelin reduces the risk of abnormal eating behaviors by increasing neuropeptide Y and γ-aminobutyric acid. In addition, ghrelin increases food intake by inhibiting fatty acid biosynthesis. However, despite the numerous studies on the role of ghrelin in the AD-related pathology and metabolic disorders, there are only a few studies that investigate the effects of ghrelin on secondary symptoms associated with AD. In this mini review, our purpose is to provide the insights of future study by organizing the previous studies for the role of ghrelin in AD-related pathology and metabolic disorders.

Indexed as

abnormal eating behaviorsAlzheimer’s diseasedepressionghrelinmetabolic syndromesleep–wake disturbances

Identifiers

PMID33071750
PMCPMC7543232

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.