Abstract:Background
Data have been accumulating in the past few years that identify vitiligo as a disorder with systemic implications.
Results and methods
In this hospital‐based, cross‐sectional, case–control study, 50 patients with non‐segmental vitiligo and 50 age‐ and sex‐matched controls underwent analysis of serum lipid profile, oxidative stress biomarkers and carotid duplex. Hydrogen peroxide (H2O2) and malondialdehyde (MDA) were significantly higher in patients than controls (p‐value < .001, <.001, respectively)… Show more
“…OS is characterized by the excessive accumulation of oxidation products and inadequate antioxidants ( Chen et al, 2021 ). There is numerous evidence that patients with vitiligo have increased oxidation product like the lipid oxidation product malondialdehyde (MDA) and the oxidative DNA damage byproducts [8-hydroxy-2-deoxyguanosine (8-OHdG)] ( Wei et al, 2013 ; Vaseghi et al, 2017 ; Azzazi et al, 2021 ). In addition, patients with vitiligo have down-regulated enzymes, such as catalase (CAT) ( Agrawal et al, 2014 ) and dysregulated superoxide dismutase (SOD) ( Koca et al, 2004 ; Khan et al, 2009 ; Ozel Turkcu et al, 2014 ), and abnormal non-enzyme defense to oxidants like the total antioxidant capacity (TAC) ( Hayran et al, 2021 ).…”
Non-segmental vitiligo (NSV) is a chronic autoimmune disease characterized by progressive depigmentation of the skin. Oxidative stress (OS) has been proposed as one among the main principal causes in the development and establishment of a sustained autoimmune state in patients with NSV. However, the disease-associated OS biomarkers in clinical practice are not well studied. In this study, we found significantly reduced antioxidant enzymes [catalase (CAT) and superoxide dismutase (SOD)], total antioxidant capacity (TAC), and increased levels of lipid oxidation product malondialdehyde (MDA) and oxidative DNA damage byproduct [8-hydroxy-2-deoxyguanosine (8-OHdG)] in serum of NSV patients compared with healthy controls (HC). Serum TAC, MDA, and 8-OHdG levels were correlated with disease activity in all patients with NSV and much lower in patients receiving conventional treatment in the past 1 year compared to that without treatment. In addition, both serum MDA and 8-OHdG levels were significantly correlated with CXCL10 expression in patients with NSV. And the serum TAC, MDA, and 8-OHdG levels were also correlated with affected body surface area and Vitiligo Area Scoring Index score in patients with NSV. This study demonstrates dysregulated OS status in patients with NSV and provides the evidence that the serum TAC, MDA, and 8-OHdG have a capacity to indicate the activity and severity in patients with NSV.
“…OS is characterized by the excessive accumulation of oxidation products and inadequate antioxidants ( Chen et al, 2021 ). There is numerous evidence that patients with vitiligo have increased oxidation product like the lipid oxidation product malondialdehyde (MDA) and the oxidative DNA damage byproducts [8-hydroxy-2-deoxyguanosine (8-OHdG)] ( Wei et al, 2013 ; Vaseghi et al, 2017 ; Azzazi et al, 2021 ). In addition, patients with vitiligo have down-regulated enzymes, such as catalase (CAT) ( Agrawal et al, 2014 ) and dysregulated superoxide dismutase (SOD) ( Koca et al, 2004 ; Khan et al, 2009 ; Ozel Turkcu et al, 2014 ), and abnormal non-enzyme defense to oxidants like the total antioxidant capacity (TAC) ( Hayran et al, 2021 ).…”
Non-segmental vitiligo (NSV) is a chronic autoimmune disease characterized by progressive depigmentation of the skin. Oxidative stress (OS) has been proposed as one among the main principal causes in the development and establishment of a sustained autoimmune state in patients with NSV. However, the disease-associated OS biomarkers in clinical practice are not well studied. In this study, we found significantly reduced antioxidant enzymes [catalase (CAT) and superoxide dismutase (SOD)], total antioxidant capacity (TAC), and increased levels of lipid oxidation product malondialdehyde (MDA) and oxidative DNA damage byproduct [8-hydroxy-2-deoxyguanosine (8-OHdG)] in serum of NSV patients compared with healthy controls (HC). Serum TAC, MDA, and 8-OHdG levels were correlated with disease activity in all patients with NSV and much lower in patients receiving conventional treatment in the past 1 year compared to that without treatment. In addition, both serum MDA and 8-OHdG levels were significantly correlated with CXCL10 expression in patients with NSV. And the serum TAC, MDA, and 8-OHdG levels were also correlated with affected body surface area and Vitiligo Area Scoring Index score in patients with NSV. This study demonstrates dysregulated OS status in patients with NSV and provides the evidence that the serum TAC, MDA, and 8-OHdG have a capacity to indicate the activity and severity in patients with NSV.
“…Oxidative stress has been a notorious factor involved in the development of various diseases, including vitiligo and metabolic syndrome, through the generation of reactive oxygen species (ROS). ROS plays a vital role in cellular events such as inflammatory response, cell growth alteration, and apoptosis [ 12 ]. Enzymatic and non-enzymatic antioxidants such as superoxide dismutase, glutathione peroxidase, and catalase are present in melanocytes whose primary function is to prevent oxidative damage.…”
Section: Reviewmentioning
confidence: 99%
“…Koca et al, in their study, showed excess free radical generation leading to peroxidative damage mediated by increased oxidative destruction of polyunsaturated fatty acid of phospholipids [ 14 ]. This oxidative destruction was supported by increased levels of malondialdehyde (MDA) and H 2 O 2 [ 12 , 14 , 15 ]. Azzazi et al and Khan et al also found decreased total antioxidant capacity in patients compared to controls.…”
Section: Reviewmentioning
confidence: 99%
“…Azzazi et al and Khan et al also found decreased total antioxidant capacity in patients compared to controls. They found a significant association between carotid intima-media thickness and MDA levels [ 12 , 15 ]. A study by Bhatti et al mentioned that oxidative stress caused the deposition of ROS in cells and tissues, leading to mitochondrial dysfunction by interacting with mitochondrial and cellular components such as DNA, protein, and lipids [ 16 ].…”
Vitiligo is an autoimmune condition primarily affecting the skin where there is destruction of melanocytes characterized by pinkish-white patches on the skin. It is associated with other autoimmune diseases such as thyroid disease, rheumatoid arthritis, diabetes mellitus, and metabolic syndrome. Metabolic syndrome is a constellation of disorders including insulin resistance, hypertension, dyslipidemia, and obesity, and is considered a leading cause of cardiovascular morbidity. Simvastatin is a potent hypolipidemic drug that also possesses immunomodulating properties and is a common drug used in dyslipidemia and cardiovascular diseases. This study aimed to assess the association between vitiligo and metabolic syndrome and explore the immunomodulating properties of simvastatin for use in vitiligo. We reviewed various articles from PubMed, ResearchGate, and Google Scholar using different keywords and Medical Subject Headings and finalized 33 studies to be used in our review. The articles selected showed a positive association between vitiligo and metabolic syndrome or one of the component diseases of metabolic syndrome. The benefits of using simvastatin were also addressed by few articles attributing to its antioxidant and immunomodulating effect. However, there was no concrete explanation justifying the association between vitiligo and metabolic syndrome due to a limited number of studies and smaller sample size. Large-scale clinical trials should be conducted to evaluate the use of simvastatin as an immunomodulator in vitiligo to prevent possible metabolic complications.
“…Karadag et al are concordant with the abovecited papers, showing lower HDL concentration, increased LDL/HDL ratio, and higher insulin resistance as measured with homeostatic model assessment-IR (HOMA-IR) [62]. A recent study by Azzazi et al has shown that a subset of patients with vitiligo is at a higher risk of developing dyslipidemia and atherosclerosis, which might increase their future risk for the development of cardiovascular disease, by means of analysis of the serum lipid profile, oxidative stress biomarkers, and carotid duplex [63]. The possible alterations of the lipid profile seem not to be limited to adults as Pietrzak et al have shown increased LDL, decreased HDL, and increased LDL/HDL ratio and triglycerides in vitiligo-affected children [64].…”
Section: Metabolic Comorbidities In Vitiligomentioning
Among disorders of pigmentation, vitiligo is the most common, with an estimated prevalence between 0.5% and 1%. The disease has gathered increased attention in the most recent years, leading to a better understanding of the disease’s pathophysiology and its implications and to the development of newer therapeutic strategies. A better, more integrated approach is already in use for other chronic inflammatory dermatological diseases such as psoriasis, for which metabolic comorbidities are well-established and part of the routine clinical evaluation. The pathogenesis of these might be linked to cytokines which also play a role in vitiligo pathogenesis, such as IL-1, IL-6, TNF-α, and possibly IL-17. Following the reports of intrinsic metabolic alterations reported by our group, in this brief review, we analyze the available data on metabolic comorbidities in vitiligo, accompanied by our single-center experience. Increased awareness of the metabolic aspects of vitiligo is crucial to improving patient care.
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