Table 3.
Author/Year | Country | Intervention | Treatment Duration | Measured Parameters | Samples | Study Group (Psoriasis/Controls) | Mean Age of Patients | Effect on the Measured Parameters | |
---|---|---|---|---|---|---|---|---|---|
1 | Akbulak et al. 2017 [75] |
Turkey | MTX 10–15 mg/week | ≥12 weeks | expression of GST and CYP enzymes | Skin biopsy samples | 43 (21/22) | 42.5 ± 10.9 | ↑GSTK1, GSTM1, GSTT1, CYP1B1, CYP2E1: in the psoriasis tissues (p < 0.05); No significant decrease after MTX treatment |
2 | Elango et al. 2013 [76] |
India | MTX 7.5 mg/week |
12 weeks | ROS, MDA, nitrate, SOD, CAT, TAS |
Venous blood, skin biopsy samples | 103 (58/45) | 46.4 ± 14.1 | ↑ROS (lesional skin), MDA (serum) After 6 and 12 weeks of treatment (p < 0.001) ↓Serum nitrite, SOD, TAS, CAT (p < 0.001) (versus controls) (no difference after therapy) |
3 | Kılıc et al. 2013 [77] |
Turkey | MTX | 8 weeks | TAS, TOS, OSI, PON-1 | Venous blood | 26 (26/0) | 45.3 ± 11.7 | No significant differences pre and post-treatment |
4 | Tekin et al. 2006 [78] |
Turkey | MTX 20 mg/week | Until the disappearance of the lesions | Nitrite-nitrate | Venous blood | 43 (22/21) | 35.0 ± 11.8 | ↓Nitrite-nitrate (p < 0.05) |
5 | Darlenski et al. 2021 [79] |
Bulgaria | NB-UVB 311 nm | 10 sessions | PASI, DLQI, skin carotenoid levels | Non-invasive | 29 (20/9) | 48.9 | ↓PASI, DLQI (p < 0.001), carotenoid levels (p > 0.05) |
6 | Darlenski et al. 2018 [80] |
Bulgaria | NB-UVB 311 nm | 14 sessions | MDA, ROS, Asc, CAT | Venous blood | 47 (22/25) | 50.9 | ↓ROS, Asc, MDA, CAT (p < 0.001) |
7 | Wacewicz et al. 2017 [81] |
Poland | NB-UVB | 20 sessions | Se, Zn, Cu, Cu/Zn, CRP, TAS | Venous blood | 118 (60/58) | 41.2 ± 12.5 | ↓Se and TAS (p < 0.05) Cu/Zn ratio, Cu, Zn—no changes after NB-UVB |
8 | Karadag et al. 2016 [82] |
Turkey | NB-UVB 311 nm | 20–36 sessions | GST, CYP | Skin biopsy samples |
54 (32/22) | 37.2 ± 14.8 | GST1K1, GST1M1, GST1O1, GST1T1, CYP1A1, CYP1B1, CYP2E1: no differences pre and post-treatment |
9 | Pektas et al. 2013 [83] |
Turkey | NB-UVB 310–315 nm | 30 sessions | hsCRP, TAS, TOS, OSI, PON-1, ARE | Venous blood | 24 (24/0) | 37.9 ± 12.3 | ↓PASI (p = 0.001) ↑TOS, OSI (p < 0.001) |
10 | Coimbra et al. 2012 [84] |
Portugal | NB-UVB: 17 pts; PUVA: 20 pts; calcipotriol: 10 pts | 12 weeks | TB, MBH, MPB3, TAS, TBA, elastase, lactoferrin, CRP | Venous blood | 113 (73/40) | 45 ± 15 | PUVA: ↓leukocytes, neutrophils, elastase, lactoferrin, CRP, TBA, TBA/TAS NB-UVB:↓elastase, lactoferrin, CRP, TBA, ↑TBA/TAS; MPB3 monomers PUVA + NB-UVB: changed MPB3 profile |
11 | Karaarslan et al. 2006 [85] |
Turkey | BB-UVB | 21 weeks | TBARS, nitrite-nitrate |
Venous blood | 52 (32/20) | 42.0 ± 11.1 | ↑TBARS (p < 0.05), nitrite-nitrate levels (p < 0.01) negative correlation total nitrite—TBARS levels post-treatment (r = −0.58, p = 0.03) |
12 | Barygina et al. 2013 [86] |
Italy | infliximab 5 mg/kg every 8 weeks | 6 months | ROS, GSH, NADPH oxidase, PCO, MDA, TAS, TBARS (lipid peroxidation) | Venous blood | 47 (29/18) | 47 ± 8 | ↓PCO, TBARS, TBARS, ROS (p < 0.05) ↑TAS (p < 0.05) |
13 | Wolk et al. 2017 [87] |
USA | tofacitinib 5 mg/10 mg twice daily | 16 weeks | HDL, LDL, PON-1, LCAT, SA-A, hsCRP | Venous blood | 161 (70 tofacitinib 5 mg, 71 tofacitinib 10 mg, 50 placebo) | 42.3–50.9 | ↑LDL, HDL (p < 0.05); TC/HDL: remained constant; PON-1, LCAT (p < 0.05) compared with placebo; ↓SA-A, hsCRP (p < 0.05) compared with placebo. |
14 | Pastore et al. 2011 [88] |
Italy | efalizumab 1 mg/kg/week | 12 weeks |
Nitrites-nitrates, MDA, TBARS, SOD, Cu, Zn, GST, CAT, acrolein-protein adducts, 9.4-HNE, SF, GF, PUFA. | Venous blood | 50 (26/24) | 42.9 | pro-inflammatory cytokines, PUFAs esterified in phospholipids of RBC membranes were not affected. ↓Nitrites–nitrates, MDA levels, CAT (in non-responders) ↑GPx, GST (in non-responders) |
15 | Campanati et al. 2012 [89] |
Italy | etanercept or adalimumab | 12 weeks | iNOS, TNF-alpha, VEGF, NO, SOD, CAT, GST, GSH | Skin biopsy samples | 12 (6/6) | 51 ± 5.8 and 52 ± 6.9 | ↓VEGF (p < 0.05, regardless of the treatment) NO (p < 0.05, regardless of the treatment) CAT (p < 0.05, for adalimumab in non lesional and perilesional skin and for etanercept in non lesional skin) GST (p < 0.05, regardless of the treatment for perilesional skin) ↑SOD (p < 0.05, for adalimumab in perilesional and lesional skin) GSH (p < 0.05, for adalimumab in non lesional skin) |
Legend: MTX—Methotrexate; ROS—reactive oxygen species; MDA—malondialdehyde; SOD—superoxide dismutase; CAT—catalase; TAS—total antioxidant status; Asc—ascorbyl radicals; PASI—psoriasis area and severity index, DLQI—dermatology life quality index; NB-UVB—narrow band ultraviolet B; TAC—total antioxidant capacity; WBC—white blood cells, PCO—protein carbonyl content; GSH—glutathione content; TBARS—thiobarbituric acid reactive substances; hsCRP—high sensitive C-reactive protein; TOS—total oxidant status; OSI—oxidative stress index; PON-1—serum paraoxonase-1; AS—arylesterase; TC—total cholesterol; LDL—low-density lipoprotein; HDL—high-density lipoprotein; ALT—alanine aminotransferase; TSH—thyroid-stimulating hormone; FAE—fumaric acid esters; GSTs—Glutathione S-transferases; AE—adverse effects, CRP—c-reactive protein, Cu—copper, Se—selenium, Zn—zinc, CBD—cannabidiol, GT—Goeckerman therapy (combined exposure of 3% crude coal tar ointment and UV radiation), BPDE—benzo[a]pyrene-7,8-diol-9,10-epoxide, BB-UVB—broad-band ultraviolet B, TBARS—thiobarbituric acid reactive substance, 4-HNE—4-hydroxy nonenal-protein, SF—stimulating factors, GF—growth factors, PUFA—polyunsaturated fatty acids, GPx—glutathione, peroxidase, l-NMMA—NG-monomethyl-l-arginine, PUVA—psoralen plus UVA, TBA—thiobarbituric acid, CRP—C-reactive protein, MBH—membrane-bound hemoglobin, TB—total bilirubin, MPB3—membrane protein band 3, MCV—mean cell volume, MCH—mean cell hemoglobin, LCAT—lecithin-cholesterol acyltransferase, SA-A—serum amyloid A, CYP—cytochrome p450, 8H2DG—8-hydroxy-2′-deoxyguanosine, 8HG—8-hydroxyguanosine, 8HGN—8-hydroxyguanine. ↑, increased. ↓, decreased.