Objective: Immunoglobulin A vasculitis (IgAV) is the most common systemic vasculitis seen in children. The aim of this study is to investigate the relationship between malondialdehyde-induced oxidative stress, antioxidant system and organ involvement in IgAV patients. Method: 32 patients and 28 healthy children were included in the study. Serum malondialdehyde, reduced glutathione, vitamin E, vitamin C, retinol, and beta-carotene levels were measured in patients (separately in both the active and remission phases) and healthy children. Results: MDA levels were significantly higher in patients with active phase while reduced glutathione and vitamin C levels were markedly lower in both the active and the remission phases. Retinol and beta-carotene levels were lower in the active phase. It was found that retinol levels were significantly lower in patients with gastrointestinal system involvement compared to those without. Vitamin C levels were significantly lower in those with kidney involvement compared to those without. Also, a negative correlation was observed between retinol levels and the number of organs involved. Conclusion: We consider that especially vitamin C and vitamin A may be used in the treatment of IgAV. However, whether the derangements of the oxidant/antioxidant balance in the direction of increased oxidative stress are consequences or causes of the events occurring in the active phase of IgAV are open to further investigation.
Amaç: İmmünoglobulin A vaskülit (IgAV) çocuklarda en sık görülen sistemik vaskülittir. Bu çalışmanın amacı, IgAV hastalarında malondialdehit kaynaklı oksidatif stres, antioksidan sistem ve organ tutulumu arasındaki ilişkiyi araştırmaktır. Yöntemler: Çalışmaya 32 hasta ve 28 sağlıklı çocuk dahil edildi. Hastalarda (hem aktif hem de remisyon fazlarında ayrı ayrı) ve sağlıklı çocuklarda serum malondialdehit, redükte glutatyon, E vitamini, C vitamini, retinol ve beta-karoten seviyeleri ölçüldü. Bulgular: Aktif fazı olan hastalarda MDA seviyeleri önemli ölçüde daha yüksekken, redükte glutatyon ve C vitamini seviyeleri hem aktif hem de remisyon fazlarında belirgin şekilde daha düşüktü. Retinol ve beta-karoten seviyeleri aktif fazda daha düşüktü. Gastrointestinal sistem tutulumu olan hastalarda retinol düzeylerinin olmayanlara göre anlamlı derecede düşük olduğu bulundu. Böbrek tutulumu olanlarda, olmayanlara göre C vitamini seviyeleri önemli ölçüde daha düşüktü. Ayrıca, retinol seviyeleri ile ilgili tutulan organ sayısı arasında negatif bir korelasyon gözlendi. Sonuç: IgAV tedavisinde özellikle C vitamini ve A vitamininin kullanılabileceğini düşünüyoruz. Bununla birlikte, oksidan / antioksidan dengesindeki artmış oksidatif stres yönündeki düzensizliklerin, IgAV'nin aktif fazında meydana gelen olayların sonuçları mı yoksa nedenleri mi olduğu daha fazla araştırmaya açıktır.
___
1.Jennette JC, Falk RJ, Bacon PA, et al. 2012 RevisedInternational Chapel Hill Consensus ConferenceNomenclature of Vasculitides. Arthritis Rheum.2013; 65: 1-11.
2.Piram M, Mahr A. Epidemiology ofimmunoglobulin A vasculitis (Henoch-Schönlein):current state of knowledge. Curr Opin Rheumatol.2013 ;25: 171-8.
3.Rigante D, Castellazzi L, Bosco A, et al. Is there acrossroad between infections, genetics, and Henoch-Schönlein purpura?. Autoimmun Rev. 2013; 12:1016-21.
4.Kattoor AJ, Pothineni NVK, Palagiri D, et al.Oxidative Stress in Atherosclerosis. CurrAtheroscler Rep. 2017; 19: 42.
5.Dalbaşı E, Gedı̇k E, Tüzün A, Obay B. Correlation ofMalondialdehyde and Antioxidant Enzyme Levelswith Peritonitis Severity in Patients withGeneralized Peritonitis. Dicle Med Journal. 2020; 47:293-03.
6.Lü JM, Lin PH, Yao Q, Chen C. Chemical andmolecular mechanisms of antioxidants:experimental approaches and model systems. J CellMol Med. 2010; 14: 840-60.
7.Narayanankutty A, Job JT, Narayanankutty V.Glutathione, an Antioxidant Tripeptide: Dual Rolesin Carcinogenesis and Chemoprevention. CurrProtein Pept Sci. 2019; 20: 907-17.
8.Engin KN. Alpha-tocopherol: looking beyond anantioxidant. Mol Vis. 2009; 15: 855-60.
9.Berger MM, Oudemans-van Straaten HM. VitaminC supplementation in the critically ill patient. CurrOpin Clin Nutr Metab Care. 2015; 18: 193-201.
10.Sies H, Stahl W. Vitamins E and C, beta-carotene,and other carotenoids as antioxidants. Am J ClinNutr. 1995; 62: 1315-21.
11.P. Padmanabhan, A. Cheema, G. Paliyath,Solanaceous Fruits Including Tomato, Eggplant, andPeppers. Encyclopedia of Food and Health, 1st edn.Oxford: Academic Press, 2016; 24-32.
12.Vance TM, Su J, Fontham ET, et al. Dietaryantioxidants and prostate cancer: a review. NutrCancer. 2013; 65: 793-801.
13.Túri S, Németh I, Torkos A, et al. Oxidative stressand antioxidant defense mechanism in glomerulardiseases. Free Radic Biol Med. 1997; 22: 161-68.
14.Demircin G, Oner A, Unver Y, et al. Erythrocytesuperoxide dismutase activity and plasmamalondialdehyde levels in children with HenochSchönlein purpura. Acta Paediatr. 1998; 87: 848-52.
15.Mills JA, Michel BA, Bloch DA, et al. The AmericanCollege of Rheumatology 1990 criteria for theclassification of Henoch-Schönlein purpura.Arthritis Rheum. 1990; 33: 1114-121.
16.Cassidy JT, Petty RE: Textbook of PediatricRheumatology: Leucocytoclastic vasculitis, 5th edn.Philadelphia, Elsevier Saunders, 2005; 496–512.
17.Ece A, Yolbaş İ, Balık H, et al. Henoch-Schönleinpurpura in childhood: Review of 214 patients, J ClinExp Invest. 2012; 3: 91-5.
18.Akça Ü, Akça G, Nalcacıoğlu H, et al. Evaluation ofepidemiological, clinical and laboratory findings inHenoch Schönlein purpura. Turkish Journal ofFamily Practice. 2020; 24: 87-94.
19.Peru H, Soylemezoglu O, Bakkaloglu SA, et al.Henoch Schonlein purpura in childhood: clinicalanalysis of 254 cases over a 3-year period. ClinRheumatol. 2008; 27:1087-92.
20.Trapani S, Micheli A, Grisolia F, et al. HenochSchonlein purpura in childhood: epidemiologicaland clinical analysis of 150 cases over a 5-yearperiod and review of literature. Semin ArthritisRheum. 2005; 35: 143-53.
21.Farley TA, Gillespie S, Rasoulpour M, et al.Epidemiology of a cluster of Henoch-Schönleinpurpura. Am J Dis Child. 1989; 143: 798-803.
22.Koçak M, Büyükkaragöz B, Can Y, et al. TheEpidemiological, Clinical and Laboratory Features of91 Children with Henoch-Schönlein Purpura. AbantMedical Journal. 2015; 4: 134-40.
23.Cakiter AU, Kucuk OS, Ozkaya DB, Topukcu B,Onsun N. Demographic characteristics, aetiology,and assessment of treatment options inleukocytoclastic vasculitis. Postepy DermatolAlergol. 2017; 34: 104-9.
24.Ekinci RMK, Balci S, Melek E, et al. Clinicalmanifestations and outcomes of 420 children withHenoch Schönlein Purpura from a single referralcenter from Turkey: A three-year experience. ModRheumatol. 2020; 30: 1039-46.
25.Buyan N, Erbaş D, Akkök N, et al. Role of freeoxygen radicals and prostanoids in the pathogenesisof Henoch-Schönlein Purpura. ProstaglandinsLeukot Essent Fatty Acids. 1998; 59: 181-4.
26.Erdoğan O, Oner A, Aydin A, et al. Effect ofvitamin E treatment on the oxidative damageoccurring in Henoch-Schönlein purpura. ActaPaediatr. 2003; 92: 546-50.
27.Ece A, Kelekçi S, Kocamaz H, et al. Antioxidantenzyme activities, lipid peroxidation, and totalantioxidant status in children with Henoch-Schönlein purpura. Clin Rheumatol. 2008; 27: 163-69.
28.Gurses D, Parlaz N, Bor Kucukatay M, et al.Evaluation of oxidative stress and erythrocyteproperties in children with henoch-shoenleinpurpura. Iran J Pediatr. 2014; 24: 166-72.