Abstract
Background
Neurodegenerative disorders such as Alzheimer’s and Parkinson’s disease inflict economic and health burdens on societies. Alzheimer’s disease (AD), the most prevalent form of dementia, is accompanied by progressive degradation of memory, decision-making, and judgment. Parkinson’s disease (PD) is characterized by resting tremor, rigidity, bradykinesia, and loss of balance. Extensive research has pinpointed inflammation as a cause of the onset and progression of both diseases. However, it has not been confirmed which one is more formidable in terms of inflammation.
Methods
To assess the extent of inflammation that is implicated in AD and PD and answer the question of which one is more inflammatory, serum levels of inflammatory biomarkers, including cytokines, chemokines, and prostaglandin E2 (PEG2), were measured in AD and PD patients as well as a healthy group.
Results
Our results showed a significant increase in IL-1α, IL-1β, IL-4, IL-6, IL-10, IL-12p70, IP-10, MCP-1, PEG2, and TNF-α in AD and PD patients compared with the control. Interestingly, IFN-γ did not manifest any significant difference in AD or PD patients compared with the control.
Conclusion
As a hallmark of our results, it could be inferred that inflammation, as the underlying etiological cause, plays a more crucial role in PD compared with AD. Based on our results, it is proposed that anti-inflammatory remedies would be putatively more effective in PD rather than AD.
Acknowledgement
We wish to sincerely thank Dr. Ali Kharazian, the head of Pars Teb Clinical Laboratory, for providing us with the control samples. We are also extremely grateful to Mrs. Azam Daraee, a senior laboratory technician of Clinical biochemistry at SBMU.
Ethics approval
The present study was conducted under the approval of the Ethics Committee of SBMU (Reference No: IR.SBMU.MSP.REC.1395.603) and in accordance with ethical principles mentioned in the Declaration of Helsinki.
Consent to participate
Prior to enrollment, written informed consent (ICF) was obtained from AD and PD patients/relatives.
Authors’ contributions
All authors contributed to the study conception, design, Material preparation, data collection and analysis. All authors read and approved the final manuscript.
Disclosure statement
No potential conflict of interest was reported by the authors.
Availability of data and material
Data are available via requests directed to the corresponding author