Serum short-chain fatty acids and its correlation with motor and non-motor symptoms in Parkinson’s disease patients
Open accessAbstract
Background: Parkinson’s disease (PD) is associated with enteric nervous system dysfunction and gut microbiota dysbiosis. Short-chain fatty acids (SCFAs), derived from gut microbiota, are supposed to anticipate PD pathogenesis via the pathway of spinal cord and vagal nerve or the circulatory system. However, the serum concentration of SCFAs in PD patients is poorly known. This study aims to investigate the exact level of SCFAs in PD patients and its correlation with Parkinson’s symptoms. Methods: 50 PD patients and 50 healthy controls were recruited, and their demographic and clinical characteristics were collected. The serum concentration of SCFAs was detected using a gas chromatography-mass spectrometer. SCFAs were compared between PD and control groups. The correlation between serum SCFAs and Parkinson’s symptoms and the potential effects of medications on the serum SCFAs was analyzed. Results: Serum propionic acid, butyric acid and caproic acid were lower, while heptanoic acid was higher in PD patients than in control subjects. However, only the serum level of propionic acid was correlated with Unified Parkinson’s Disease Rating Scale (UPDRs) part III score (R = -0.365, P = 0.009), Mini-mental State Examination (MMSE) score (R = -0.416, P = 0.003), and Hamilton Depression Scale (HAMD) score (R = 0.306, P = 0.03). There was no correlation between other serum SCFAs and motor complications. The use of trihexyphenidyl or tizanidine increased the serum concentration of propionic acid. Conclusions: Serum SCFAs are altered in PD patients, and the decrease of serum propionic acid level is correlated with motor symptoms, cognitive ability and non-depressed state. Thus, the gut microbial-derived SCFAs potentially affect Parkinson’s symptoms through the blood circulation. Propionic acid supplementation might ameliorate motor and non-motor symptoms of PD patients, although clinical trials are needed to test this hypothesis.
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In vivo, MPTP-treated mice receiving propionate show better performance in the stepping test, cylinder test and whisker test.
“in vivo, MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine; a prodrug of the neurotoxin MPP+)-treated mice receiving propionate show a better performance in the stepping test, cylinder test and whisker test, in line with previous data [109,110]”
From The Interplay between Gut Microbiota and Parkinson’s Disease: Implications on Diagnosis and Treatment (2022) · cites this paper as [110]
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Self-citation
- Authors
- Wu, G., Jiang, Z., Pu, Y., Chen, S., Wang, T., Wang, Y., Xu, X., Wang, S., Jin, M., Yao, Y., Liu, Y., Ke, S., & Liu, S.
- Affiliations
- Wenzhou Medical University (CN)
- Shaoxing University (CN)
- Corresponding author
- Ke, Shaofa
- Liu, Suzhi
- Venue
- BMC Neurology
- Published
- 2022-01-07
- Volume
- 22
- Issue
- 1
- Pages
- 13-13
- ISSN
- 1471-2377 (ISSN-L)
- PMC
- PMC8740341
- OpenAlex
- W4205973174
- Cited by
- 67
- References
- 38
- Citations by year
- 2026: 8 · 2025: 20 · 2024: 16 · 2023: 8 · 2022: 15
- FWCI
- 7.76
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- BMC Neurology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Neuroscience › Neurology › Neurological diseases and metabolism
- Keywords
- Parkinson's disease, short-chain fatty acids, propionic acid, gut microbiota, motor symptoms, non-motor symptoms, cognitive function, depression, heptanoic acid, butyrate, hexanoic acid, trihexyphenidyl, tizanidine, enteric nervous system
- MeSH terms
- Gastrointestinal Microbiome, Cognition, Fatty Acids, Volatile, Humans, Parkinson Disease
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