PMID- 33527053 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20210203 IS - 2168-8184 (Print) IS - 2168-8184 (Electronic) IS - 2168-8184 (Linking) VI - 12 IP - 12 DP - 2020 Dec 30 TI - Can Pioglitazone Safeguard Patients of Lichen Planus Against Homocysteine Induced Accelerated Cardiovascular Aging and Reduced Myocardial Performance: A Systematic Review. PG - e12372 LID - 10.7759/cureus.12372 [doi] LID - e12372 AB - Lichen planus (L.P.) is a long-standing mucocutaneous inflammatory condition. A less familiar but essential illness association is increased arterial stiffness, endothelial dysfunction, and advanced atherosclerosis. Enhanced cardiac reconditioning and reduced performance of the heart have been suggested. Thiazolidinediones were commenced to manage hyperglycemia in diabetes mellitus. Recently, the class attained popularity after its action on vascular physiology was discovered. With this review, we attempted to explore whether an antidiabetic drug, pioglitazone (PIO), a peroxisome proliferator‑activated receptor gamma (PPAR gamma) agonist, can defend patients of lichen planus against increased arterial stiffness and cardiac changes. We methodically screened numerous databases using focused words and phrases for relevant articles. After a comprehensive exploration, we applied the inclusion and exclusion criteria and performed a quality appraisal. Items retained were exhaustively studied. High homocysteine (HHcy) levels in lichen planus play a significant role in modifying the arteries and leading to their dysfunction. Not only does homocysteine affect the precursor cells, but it also increases the free radical damage. Arterial damage and upraised resistance encountered by the heart reduce its performance. After an exhaustive analysis, in our opinion, pioglitazone works in various miscellaneous ways to mitigate the homocysteine mediated changes. Early inclusion of the drug in managing patients with lichen planus seems promising in minimizing the harmful effects of high homocysteine. Evaluating the risk-benefit ratio, we believe that a trial of pioglitazone could be given to patients without underlying cardiac conditions. CI - Copyright (c) 2020, Balani et al. FAU - Balani, Prachi AU - Balani P AD - Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA. FAU - Lopez, Angel R AU - Lopez AR AD - Psychiatry, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA. FAU - Nobleza, Chelsea Mae N AU - Nobleza CMN AD - Neurology, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA. FAU - Siddiqui, Mariah AU - Siddiqui M AD - Neurology, St. George's University, True Blue, GRD. AD - Neurology, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA. FAU - Shah, Parth V AU - Shah PV AD - Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA. FAU - Khan, Safeera AU - Khan S AD - Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA. LA - eng PT - Journal Article PT - Review DEP - 20201230 PL - United States TA - Cureus JT - Cureus JID - 101596737 PMC - PMC7842239 OTO - NOTNLM OT - arterial aging OT - arterial stiffness OT - cardiac remodelling OT - homoscysteine OT - left ventricle OT - lichen planus OT - microcirculaiton and inflammation OT - myocardial performance index OT - pioglitazone OT - thiazolidinediones COIS- The authors have declared that no competing interests exist. EDAT- 2021/02/03 06:00 MHDA- 2021/02/03 06:01 PMCR- 2020/12/30 CRDT- 2021/02/02 06:10 PHST- 2021/02/02 06:10 [entrez] PHST- 2021/02/03 06:00 [pubmed] PHST- 2021/02/03 06:01 [medline] PHST- 2020/12/30 00:00 [pmc-release] AID - 10.7759/cureus.12372 [doi] PST - epublish SO - Cureus. 2020 Dec 30;12(12):e12372. doi: 10.7759/cureus.12372.