Recent research progress on metabolic syndrome and risk of Parkinson’s disease
Author:
Li Lin-yi1, Liu Shu-fen1, Zhuang Jian-long2, Li Mi-mi1, Huang Zheng-ping1, Chen Yan-hong3, Chen Xiang-rong4, Chen Chun-nuan1, Lin Shu56, Ye Li-chao1
Affiliation:
1. Department of Neurology , The Second Affiliated Hospital, Fujian Medical University , No. 34 North Zhongshan Road , Quanzhou 362000 , Fujian Province , China 2. Prenatal Diagnosis Center, Quanzhou Women’s and Children’s Hospital , Quanzhou 362000 , China 3. Department of Neurology , Shishi General Hospital , Quanzhou 362000 , Fujian Province , China 4. Department of Neurosurgery , The Second Affiliated Hospital, Fujian Medical University , Quanzhou 362000 , Fujian Province , China 5. Centre of Neurological and Metabolic Research, The Second Affiliated Hospital of Fujian Medical University , Quanzhou 362000 , Fujian Province , China 6. Group of Neuroendocrinology, Garvan Institute of Medical Research , 384 Victoria St, Sydney , NSW , Australia
Abstract
Abstract
Parkinson’s disease (PD) is one of the most widespread neurodegenerative diseases. PD is associated with progressive loss of substantia nigra dopaminergic neurons, including various motor symptoms (e.g., bradykinesia, rigidity, and resting tremor), as well as non-motor symptoms (e.g., cognitive impairment, constipation, fatigue, sleep disturbance, and depression). PD involves multiple biological processes, including mitochondrial or lysosomal dysfunction, oxidative stress, insulin resistance, and neuroinflammation. Metabolic syndrome (MetS), a collection of numerous connected cerebral cardiovascular conditions, is a common and growing public health problem associated with many chronic diseases worldwide. MetS components include central/abdominal obesity, systemic hypertension, diabetes, and atherogenic dyslipidemia. MetS and PD share multiple pathophysiological processes, including insulin resistance, oxidative stress, and chronic inflammation. In recent years, MetS has been linked to an increased risk of PD, according to studies; however, the specific mechanism remains unclear. Researchers also found that some related metabolic therapies are potential therapeutic strategies to prevent and improve PD. This article reviews the epidemiological relationship between components of MetS and the risk of PD and discusses the potentially relevant mechanisms and recent progress of MetS as a risk factor for PD. Furthermore, we conclude that MetS-related therapies are beneficial for the prevention and treatment of PD.
Funder
Science and Technology Bureau of Quanzhou Fujian Provincial Department of Science and Technology Fujian Provincial Health Technology Project Natural Science Foundation of Fujian Province,China
Publisher
Walter de Gruyter GmbH
Subject
General Neuroscience
Reference152 articles.
1. Abbott, R.D., Ross, G.W., White, L.R., Nelson, J.S., Masaki, K.H., Tanner, C.M., Curb, J.D., Blanchette, P.L., Popper, J.S., and Petrovitch, H. (2002). Midlife adiposity and the future risk of Parkinson’s disease. Neurology 59: 1051–1057, https://doi.org/10.1212/wnl.59.7.1051. 2. Abdelsalam, R.M. and Safar, M.M. (2015). Neuroprotective effects of vildagliptin in rat rotenone Parkinson’s disease model: role of RAGE-NFκB and Nrf2-antioxidant signaling pathways. J. Neurochem. 133: 700–707, https://doi.org/10.1111/jnc.13087. 3. Armutcu, F., Ataymen, M., Atmaca, H., and Gurel, A. (2008). Oxidative stress markers, C-reactive protein and heat shock protein 70 levels in subjects with metabolic syndrome. Clin. Chem. Lab. Med. 46: 785–790, https://doi.org/10.1515/cclm.2008.166. 4. Athauda, D., Maclagan, K., Skene, S.S., Bajwa-Joseph, M., Letchford, D., Chowdhury, K., Hibbert, S., Budnik, N., Zampedri, L., Dickson, J., et al.. (2017). Exenatide once weekly versus placebo in Parkinson’s disease: a randomised, double-blind, placebo-controlled trial. Lancet 390: 1664–1675, https://doi.org/10.1016/s0140-6736(17)31585-4. 5. Aviles-Olmos, I., Limousin, P., Lees, A., and Foltynie, T. (2013). Parkinson’s disease, insulin resistance and novel agents of neuroprotection. Brain 136: 374–384, https://doi.org/10.1093/brain/aws009.
Cited by
11 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|