Iron Dysregulation and Inflammagens Related to Oral and Gut Health Are Central to the Development of Parkinson's Disease

Biomolecules. 2020 Dec 29;11(1):30. doi: 10.3390/biom11010030.


Neuronal lesions in Parkinson's disease (PD) are commonly associated with α-synuclein (α-Syn)-induced cell damage that are present both in the central and peripheral nervous systems of patients, with the enteric nervous system also being especially vulnerable. Here, we bring together evidence that the development and presence of PD depends on specific sets of interlinking factors that include neuroinflammation, systemic inflammation, α-Syn-induced cell damage, vascular dysfunction, iron dysregulation, and gut and periodontal dysbiosis. We argue that there is significant evidence that bacterial inflammagens fuel this systemic inflammation, and might be central to the development of PD. We also discuss the processes whereby bacterial inflammagens may be involved in causing nucleation of proteins, including of α-Syn. Lastly, we review evidence that iron chelation, pre-and probiotics, as well as antibiotics and faecal transplant treatment might be valuable treatments in PD. A most important consideration, however, is that these therapeutic options need to be validated and tested in randomized controlled clinical trials. However, targeting underlying mechanisms of PD, including gut dysbiosis and iron toxicity, have potentially opened up possibilities of a wide variety of novel treatments, which may relieve the characteristic motor and nonmotor deficits of PD, and may even slow the progression and/or accompanying gut-related conditions of the disease.

Keywords: Parkinson’s disease; amyloid and α-synuclein; bacteria; gingipains; iron; lipopolysaccharides.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Dysbiosis / complications
  • Dysbiosis / metabolism*
  • Dysbiosis / physiopathology
  • Gastrointestinal Microbiome
  • Humans
  • Inflammation / complications
  • Inflammation / metabolism*
  • Inflammation / physiopathology
  • Iron / metabolism*
  • Mouth / microbiology
  • Oxidative Stress
  • Parkinson Disease / etiology
  • Parkinson Disease / metabolism*
  • Parkinson Disease / physiopathology
  • alpha-Synuclein / metabolism


  • alpha-Synuclein
  • Iron