Cutaneous and Ocular Toxicology最新文献

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Understanding the impact of risankizumab on keratinocyte-derived IL-23A in a novel organotypic 3D skin model containing IL-23A responsive and IL-17A producing γδ-T-cells. 在一种含有IL-23A反应性和IL-17A产生性γδ-T细胞的新型有机三维皮肤模型中了解利坦珠单抗对角质细胞衍生的IL-23A的影响。
IF 1.6 4区 医学
Cutaneous and Ocular Toxicology Pub Date : 2024-06-01 Epub Date: 2024-02-02 DOI: 10.1080/15569527.2024.2310243
Laura Huth, Philipp M Amann, Yvonne Marquardt, Manuela Jansen, Jens Malte Baron, Sebastian Huth
{"title":"Understanding the impact of risankizumab on keratinocyte-derived IL-23A in a novel organotypic 3D skin model containing IL-23A responsive and IL-17A producing γδ-T-cells.","authors":"Laura Huth, Philipp M Amann, Yvonne Marquardt, Manuela Jansen, Jens Malte Baron, Sebastian Huth","doi":"10.1080/15569527.2024.2310243","DOIUrl":"10.1080/15569527.2024.2310243","url":null,"abstract":"<p><strong>Purpose: </strong>To study the effects of the anti-IL-23A antibody risankizumab on the IL-36γ/IL-23A/IL-17A signalling cascade we used a newly developed 3D skin model consisting of primary human keratinocytes, fibroblasts and γδ-T-cells.</p><p><strong>Methods: </strong>In this <i>in vitro</i> study we developed new full-thickness 3D skin models containing normal human epidermal keratinocytes (NHEK), normal human dermal fibroblasts (NHDF) and IL-23A responsive and IL-17A producing γδ-T-cells. The effects of IL-36γ stimulation with and without risankizumab treatment on IL-23A and IL-17A expression were examined at the RNA and protein levels.</p><p><strong>Results: </strong>In preliminary monolayer experiments stimulation of γδ-T-cells with IL-23A promoted the IL-17A expression that was inhibited after risankizumab treatment. Using 3D skin models containing γδ-T-cells, we found that stimulation with IL-36γ significantly increased not only IL-23A but also IL-17A expression. These effects were inhibited by concomitant treatment with risankizumab.</p><p><strong>Conclusions: </strong>Our results showed that blockade of IL-23A has inhibitory effects on the IL-36γ/IL-23A feedforward loop. Our newly developed 3D skin model containing IL-23A responsive and IL-17A producing γδ-T-cells enables molecular analysis of targeted therapies aimed at the IL-36γ/IL-23A/IL-17A signalling cascade in psoriasis.</p>","PeriodicalId":11023,"journal":{"name":"Cutaneous and Ocular Toxicology","volume":" ","pages":"124-128"},"PeriodicalIF":1.6,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139570103","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enhanced Sun Protection Factor Of Octocrylene With Green Tea And Bhringraj Extracts 绿茶和布林拉杰提取物增强了辛二烯的防晒系数
IF 1.6 4区 医学
Cutaneous and Ocular Toxicology Pub Date : 2024-04-12 DOI: 10.1080/15569527.2024.2340440
Pasupathi M., Natarajan B., Kumar T.
{"title":"Enhanced Sun Protection Factor Of Octocrylene With Green Tea And Bhringraj Extracts","authors":"Pasupathi M., Natarajan B., Kumar T.","doi":"10.1080/15569527.2024.2340440","DOIUrl":"https://doi.org/10.1080/15569527.2024.2340440","url":null,"abstract":"The overexposure of human skin to ultraviolet radiation (UVR) can trigger photodamage, UV burn, pigmentation, erythema, and enhance the chance of dermal carcinoma. UVR causes DNA damage, leading to...","PeriodicalId":11023,"journal":{"name":"Cutaneous and Ocular Toxicology","volume":"2 1","pages":""},"PeriodicalIF":1.6,"publicationDate":"2024-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140590903","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evaluation of Isotretinoin effects on depression, sleep apnea and sleep quality 评估异维A酸对抑郁、睡眠呼吸暂停和睡眠质量的影响
IF 1.6 4区 医学
Cutaneous and Ocular Toxicology Pub Date : 2024-04-12 DOI: 10.1080/15569527.2024.2340435
Ozge Mine Orenay, Berkay Temel, Arcan Kivanc Capci, Zulal Inci Bal, Nermin Karaosmanoglu
{"title":"Evaluation of Isotretinoin effects on depression, sleep apnea and sleep quality","authors":"Ozge Mine Orenay, Berkay Temel, Arcan Kivanc Capci, Zulal Inci Bal, Nermin Karaosmanoglu","doi":"10.1080/15569527.2024.2340435","DOIUrl":"https://doi.org/10.1080/15569527.2024.2340435","url":null,"abstract":"Background: Isotretinoin is used to treat severe acne, treatment-resistant moderate acne, and acne that leads to scarring or psychological distress. It has many side effects and is also associated ...","PeriodicalId":11023,"journal":{"name":"Cutaneous and Ocular Toxicology","volume":"95 1","pages":""},"PeriodicalIF":1.6,"publicationDate":"2024-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140590889","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effect of isotretinoin treatment on inflammatory and hematological parameters in patients with acne vulgaris. 异维甲酸治疗对寻常痤疮患者炎症和血液学参数的影响。
IF 1.6 4区 医学
Cutaneous and Ocular Toxicology Pub Date : 2024-03-01 Epub Date: 2023-10-14 DOI: 10.1080/15569527.2023.2268166
Mustafa Esen
{"title":"Effect of isotretinoin treatment on inflammatory and hematological parameters in patients with acne vulgaris.","authors":"Mustafa Esen","doi":"10.1080/15569527.2023.2268166","DOIUrl":"10.1080/15569527.2023.2268166","url":null,"abstract":"<p><strong>Purpose: </strong>Although the inflammatory and anti-inflammatory effects of isotretinoin (ISO) treatment in patients with acne vulgaris have been discussed in the literature in recent years, no sensitive and specific marker has been found in studies so far. Neutrophil/HDL (high-density lipoprotein) (NHR), lymphocyte/HD L(LHR), platelet/HDL (PHR), and lymphocyte/monocyte (LMR) are new biomarkers related to inflammation. Triglyceride/HDL (TG/HDL), LDL/HDL, and total cholesterol/HDL have been shown to be cardiometabolic risk factors predicting both cardiovascular disease risk and metabolic risk, rather than just a simple dyslipidemia scale. To our knowledge, the relationship between these parameters and ISO treatment has never been studied before. We aimed to evaluate the immuno-inflammatory response of ISO treatment in patients with acne vulgaris with NHR, LHR, PHR, LMR, TG/HDL, LDL/HDL, and total cholesterol/HDL parameters.</p><p><strong>Materials and methods: </strong>In this study, 153 patients who received oral ISO treatment for at least 3 months with a diagnosis of moderate-severe acne vulgaris were evaluated retrospectively. Patients were given oral isotretinoin at a dose of 0.5-1 mg/kg. Pre and post-treatment leukocyte (WBC), neutrophil (NE), lymphocyte (LY), platelet (PLT), red cell distribution width (RDW), plateletcrit (PCT), neutrophil/lymphocyte (NLR), platelet/lymphocyte (PLR), mean platelet volume (MPV), monocyte/lymphocyte (MLR), LMR, total cholesterol, LDL cholesterol, HDL cholesterol, triglyceride, MHR, NHR, LHR, PHR, TG/HDL, total cholesterol/HDL, LDL/HDL parameters were evaluated.</p><p><strong>Results: </strong>It was found that post-treatment WBC and MPV values increased statistically significantly; NLR, neutrophil, and PCT values, on the other hand, decreased significantly (<i>p</i> < 0.05). No statistically significant change was detected in PLR, MLR, LMR, MHR, NHR, LHR, PHR, lymphocyte, monocyte, platelet, and RDW parameters (<i>p</i> > 0.05). It was determined that post-treatment total cholesterol, triglyceride, VLDL, and LDL levels increased statistically significantly; however, the HDL level decreased significantly (<i>p</i> < 0.05). Levels of total cholesterol/HDL, TG/HDL, and LDL/HDL were also found to increase statistically significantly (<i>p</i> < 0.05).</p><p><strong>Conclusion: </strong>Our study suggests that the MPV and NLR ratio as biomarkers can be used as indicators of atherosclerosis-related inflammation due to ISO treatment, but the MHR, NHR, LHR, PHR, MLR, LMR ratios cannot be used. Moreover, we believe that the ratios of TG/HDL, LDL/HDL, and total cholesterol/HDL offer a new contribution as indicators of cardiovascular risk and systemic inflammation related to ISO treatment.</p>","PeriodicalId":11023,"journal":{"name":"Cutaneous and Ocular Toxicology","volume":" ","pages":"27-32"},"PeriodicalIF":1.6,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41194356","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Retinal nerve fiber layer and ganglion cell complex thickness in diabetic smokers without diabetic retinopathy. 无糖尿病视网膜病变的糖尿病吸烟者的视网膜神经纤维层和神经节细胞复合体厚度。
IF 1.6 4区 医学
Cutaneous and Ocular Toxicology Pub Date : 2024-03-01 Epub Date: 2023-10-24 DOI: 10.1080/15569527.2023.2268162
Kübra Özata Gündoğdu, Emine Doğan, Erkan Çelik, Gürsoy Alagöz
{"title":"Retinal nerve fiber layer and ganglion cell complex thickness in diabetic smokers without diabetic retinopathy.","authors":"Kübra Özata Gündoğdu, Emine Doğan, Erkan Çelik, Gürsoy Alagöz","doi":"10.1080/15569527.2023.2268162","DOIUrl":"10.1080/15569527.2023.2268162","url":null,"abstract":"<p><strong>Purpose: </strong>To compare the thickness of the retinal nerve fiber layer (RNFL) and macular ganglion cell-inner plexiform layer (GC-IPL) in smoker and nonsmoker diabetics without diabetic retinopathy.</p><p><strong>Materials and methods: </strong>Patients with diabetes were divided into two groups according to their smoking status: Group 1 consisted of 38 smoker diabetics who had chronically smoked more than 20 cigarettes per day for more than five years; Group 2 consisted of 38 nonsmoker diabetics. After a detailed ophthalmologic examination, the mean and regional (superior, supratemporal, inferior, inferotemporal, temporal, nasal, superonasal, and inferonasal) RNFL and GC-IPL thicknesses were measured with spectral-domain optic coherence tomography (SD-OCT) and compared between groups.</p><p><strong>Results: </strong>The mean age was 54.7 ± 10.5 and 51.2 ± 9.7 years in the smoker and nonsmoker groups, respectively (<i>p</i> = 0.14). Gender, duration of diabetes, and the mean axial length were similar between groups (<i>p:</i>0.43, <i>p</i>:0.54, <i>p</i>: 0.52, respectively). Mean RNFL thickness was 89.1 ± 8.0 µm in the smoker group and 93.4 ± 7.0 µm in the nonsmoker group, and it was significantly thinner in the smoker group (<i>p</i> = 0.01). The temporal RNFL thickness in the smoker group was thinner than in the nonsmoker group (<i>p</i> = 0.02). There was no difference in superior, inferior, and nasal RNFL thicknesses between the groups (<i>p</i> = 0.31, <i>p</i> = 0.12, <i>p</i> = 0.39, respectively). The mean macular GC-IPL thickness of the smoker and nonsmoker groups was 78.53 ± 15.74 µm and 83.08 ± 5.85 µm, respectively (<i>p</i> = 0.09). Superior, superonasal, inferonasal, inferior, inferotemporal, and superotemporal quadrant GC-IPL thicknesses were similar between the groups (<i>p</i> = 0.07, <i>p</i> = 0.60, <i>p</i> = 0.55, <i>p</i> = 0.77, <i>p</i> = 0.71, <i>p =</i> 0.08, respectively). The groups showed no difference in minimum GC-IPL thickness (p = 0.43). There was a significant negative correlation between smoking exposure and mean, inferior quadrant RNFL thicknesses in the smoker group (<i>p</i> = 0.04, r= -0.32, and <i>p</i> = 0.01, r= -0.39, respectively).</p><p><strong>Conclusion: </strong>Mean RNFL thickness was significantly thinner in smoker diabetics. Although not statistically significant, especially mean, superior, and superotemporal GC-IPL was thinner in smoker diabetics. The results suggest a potential association between the coexistence of diabetes and smoking with alterations in RNFL and GC-IPL thickness.</p>","PeriodicalId":11023,"journal":{"name":"Cutaneous and Ocular Toxicology","volume":" ","pages":"22-26"},"PeriodicalIF":1.6,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49689212","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Allergic contact dermatitis to lip care cosmetic products - a systematic review. 唇部护理化妆品的过敏性接触性皮炎——一项系统综述。
IF 1.6 4区 医学
Cutaneous and Ocular Toxicology Pub Date : 2024-03-01 Epub Date: 2023-10-30 DOI: 10.1080/15569527.2023.2275022
Biplab Pal, Sweta Kumari, Alka Kumari, Sachin Kumar Singh, Harish Babbar
{"title":"Allergic contact dermatitis to lip care cosmetic products - a systematic review.","authors":"Biplab Pal, Sweta Kumari, Alka Kumari, Sachin Kumar Singh, Harish Babbar","doi":"10.1080/15569527.2023.2275022","DOIUrl":"10.1080/15569527.2023.2275022","url":null,"abstract":"<p><p><b>Aim:</b> Lip care cosmetics products are any external preparation used by people to prevent drying, chapping, dullness, and beautification of lips. This study aimed to review the literature on allergic reactions induced by different types of lip care cosmetic products. <b>Methods:</b> A literature search was performed in PubMed from inception to June 2022. The study included articles published in English and available in full text. References of illegible articles were searched. Studies describing any patient who developed allergic contact dermatitis after the application of lip care cosmetic products were included. <b>Results:</b> A total of 47 reports consisting of 58 individuals experienced allergic reactions to lip care products. Several lip care cosmetics products, such as lipsticks, lip balms, lip salve, lip gloss, lip liner, and lip plumper, were found to be associated with allergic reactions. The most common ingredients that caused the allergic contact dermatitis were castor oil, benzophenone-3, gallate, wax, and colophony. <b>Conclusions:</b> Lip care cosmetics products contain several components that have been associated with allergic reactions. Awareness needs to be created among the general public and dermatologists regarding the presence of possible allergens in lip care cosmetic products.</p>","PeriodicalId":11023,"journal":{"name":"Cutaneous and Ocular Toxicology","volume":" ","pages":"13-21"},"PeriodicalIF":1.6,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71410968","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Time to treat the climate and nature crisis as one indivisible global health emergency. 是时候将气候和自然危机作为一个不可分割的全球健康紧急事件来对待了。
IF 1.6 4区 医学
Cutaneous and Ocular Toxicology Pub Date : 2024-03-01 Epub Date: 2023-11-06 DOI: 10.1080/15569527.2023.2276593
Kamran Abbasi, Parveen Ali, Virginia Barbour, Thomas Benfield, Kirsten Bibbins-Domingo, Gregory E Erhabor, Stephen Hancocks, Richard Horton, Laurie Laybourn-Langton, Robert Mash, Peush Sahni, Wadeia Mohammad Sharief, Paul Yonga, Chris Zielinski
{"title":"Time to treat the climate and nature crisis as one indivisible global health emergency.","authors":"Kamran Abbasi, Parveen Ali, Virginia Barbour, Thomas Benfield, Kirsten Bibbins-Domingo, Gregory E Erhabor, Stephen Hancocks, Richard Horton, Laurie Laybourn-Langton, Robert Mash, Peush Sahni, Wadeia Mohammad Sharief, Paul Yonga, Chris Zielinski","doi":"10.1080/15569527.2023.2276593","DOIUrl":"https://doi.org/10.1080/15569527.2023.2276593","url":null,"abstract":"","PeriodicalId":11023,"journal":{"name":"Cutaneous and Ocular Toxicology","volume":"43 1","pages":"1-4"},"PeriodicalIF":1.6,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140058906","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Literature analysis of cutaneous adverse reactions induced by tislelizumab. tislelizumab引起皮肤不良反应的文献分析。
IF 1.6 4区 医学
Cutaneous and Ocular Toxicology Pub Date : 2024-03-01 Epub Date: 2023-11-01 DOI: 10.1080/15569527.2023.2275028
Qingli Guo, Lili Jin, Tingting Zhang, Ruihao Gao, Kaili Zou, Min Fu, Hengtai Bi, Junyao Zhang, Min Zhang
{"title":"Literature analysis of cutaneous adverse reactions induced by tislelizumab.","authors":"Qingli Guo, Lili Jin, Tingting Zhang, Ruihao Gao, Kaili Zou, Min Fu, Hengtai Bi, Junyao Zhang, Min Zhang","doi":"10.1080/15569527.2023.2275028","DOIUrl":"10.1080/15569527.2023.2275028","url":null,"abstract":"<p><strong>Objective: </strong>Tislelizumab may induce immune-related adverse events, especially adverse skin events. Early detection and timely intervention of cutaneous adverse events are crucial to improve patients' quality of life and reduce the disruption of therapeutic regimens. This study aimed to determine the clinical characteristics of cutaneous adverse reactions to tislelizumab and offer a reference for its rational clinical use.</p><p><strong>Methods: </strong>Case reports of cutaneous adverse reactions induced by tislelizumab were collected from the relevant databases (up to 31 March 2023). Patient age, sex, primary disease, medication use, occurrence of adverse skin conditions, treatment, and outcomes were recorded and descriptively analysed.</p><p><strong>Results: </strong>A total of 13 patients were enrolled, including six males and seven females, aged 55-79 years, with a median age of 75 years and a mean age of 70.92 ± 8.84 years. The original disease was lung carcinoma in none patients, cervical carcinoma in two, and urothelial carcinoma and squamous cell carcinoma in one each. The time from the initiation of medication use to the occurrence of cutaneous adverse reactions ranged from 7 to 177 days. Among the 13 patients, 10 showed improvement after drug withdrawal or symptomatic treatment. Two patients died (one died of disease progression and multiorgan failure, one died of acute coronary syndrome), and one patient's adverse skin reactions persisted without treatment.</p><p><strong>Conclusions: </strong>Tislelizumab-related cutaneous adverse reactions mostly occur after several days to months of treatment. In clinical practice, evaluation and monitoring should be strengthened. More attention should be paid to erythema and rashes, which may be signs of serious adverse skin reactions. Early detection and intervention can ensure the safe use of drugs and provide greater clinical benefits to patients.</p>","PeriodicalId":11023,"journal":{"name":"Cutaneous and Ocular Toxicology","volume":" ","pages":"52-57"},"PeriodicalIF":1.6,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71421611","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The effect of IL17 and IL23 inhibitors on hematological parameters and C-reactive protein in psoriasis patients. IL17和IL23抑制剂对银屑病患者血液学参数和C反应蛋白的影响。
IF 1.6 4区 医学
Cutaneous and Ocular Toxicology Pub Date : 2024-03-01 Epub Date: 2023-10-28 DOI: 10.1080/15569527.2023.2275020
Mustafa Esen
{"title":"The effect of IL17 and IL23 inhibitors on hematological parameters and C-reactive protein in psoriasis patients.","authors":"Mustafa Esen","doi":"10.1080/15569527.2023.2275020","DOIUrl":"10.1080/15569527.2023.2275020","url":null,"abstract":"<p><strong>Introduction: </strong>In the quest for objective biomarkers for psoriasis, the neutrophil/lymphocyte ratio (NLR), platelet/lymphocyte ratio (PLR), C-reactive protein (CRP), and mean platelet volume (MPV) have been used to assess disease severity, treatment efficacy, and follow-up in psoriasis, and their relationship with the Psoriasis Area Severity Index (PASI) has been investigated.</p><p><strong>Purpose: </strong>The evaluation of pre-treatment, 3rd and 6th-month levels of NLR, PLR, MPV, and CRP along with PASI scores in psoriasis patients treated with secukinumab, ixekizumab, risankizumab, and guselkumab.</p><p><strong>Materials and methods: </strong>In our study, 83 patients aged 18 and over, who were followed up with moderate-severe plaque type psoriasis vulgaris and psoriatic arthritis and received secukinumab, ixekizumab, risankizumab, and guselkumab treatment in the chronic skin diseases clinic of Fırat University Faculty of Medicine Hospital between January 2019 and 2023, were evaluated retrospectively.</p><p><strong>Results: </strong>Post-treatment leukocyte, neutrophil, lymphocyte, platelet, CRP, and PASI values were statistically significantly lower in all biological agent groups and all patients. The post-treatment NLR value was statistically significantly higher in all patients and in the group using ixekizumab. The post-treatment PLR value was statistically significantly higher in the group using guselkumab and ixekizumab and in all patients. The post-treatment MPV was statistically significantly higher in all patients and in the group using secukinumab. No correlation was found between post-treatment PASI and other values (p > 0.05). There was no statistically significant difference between the post-treatment 6-month values among all biological agent groups. The effects of different drugs on outcomes after treatment were found to be similar (p > 0.05).</p><p><strong>Conclusion: </strong>Our study supports the view that MPV and CRP can be used in patients with psoriasis using IL17 and IL23 inhibitors, while NLR and PLR parameters derived from blood count may not be used to evaluate treatment response, contrary to other studies.</p>","PeriodicalId":11023,"journal":{"name":"Cutaneous and Ocular Toxicology","volume":" ","pages":"38-45"},"PeriodicalIF":1.6,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"66783648","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Potential inhibition of 12-O-tetradecanoylphorbol-13-acetate-induced inflammation, hyperproliferation, and hyperplasiogenic responses by celecoxib in mouse skin. 塞来昔布对 12-O- 十四碳酰樟脑-13-乙酸酯诱导的小鼠皮肤炎症、过度增殖和增生反应的潜在抑制作用。
IF 1.6 4区 医学
Cutaneous and Ocular Toxicology Pub Date : 2024-03-01 Epub Date: 2024-01-01 DOI: 10.1080/15569527.2023.2295843
Shakilur Rahman, Rizwanul Haque, Sheikh Raisuddin
{"title":"Potential inhibition of 12-<i>O</i>-tetradecanoylphorbol-13-acetate-induced inflammation, hyperproliferation, and hyperplasiogenic responses by celecoxib in mouse skin.","authors":"Shakilur Rahman, Rizwanul Haque, Sheikh Raisuddin","doi":"10.1080/15569527.2023.2295843","DOIUrl":"10.1080/15569527.2023.2295843","url":null,"abstract":"<p><strong>Purpose: </strong>Skin exposure to noxious agents leads to cutaneous lesion marked by an increase in inflammation, cellular proliferation, and hyperplasiogenic reactions. Studies have demonstrated that these damages breach the skin integrity resulting in the aetiology of various cutaneous disorders like atopic dermatitis, eczema, psoriasis, and development of non-melanoma skin cancer. Celecoxib, a cyclooxygenase-2 (COX-2) inhibitor, is an effective treatment for a variety of inflammatory diseases. Its importance in the therapy of skin problems, however, remains under appreciated.</p><p><strong>Methods: </strong>We tested efficacy of topically applied celecoxib in mitigating skin inflammation, cellular proliferation, and hyperplasia induced by the phorbol ester 12-<i>O</i>-tetradecanoylphorbol-13-acetate (TPA) in Swiss albino mice.</p><p><strong>Results: </strong>Celecoxib (5 and 10 μmol) markedly reduced TPA (10 nmol) induced prostaglandin E<sub>2</sub> (PGE<sub>2</sub>) production, oedema formation, myeloperoxidase (MPO) activity, and levels of pro-inflammatory cytokines such as tumour necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1β), and interleukin-6 (IL-6). It also resulted in a considerable decrease in ornithine decarboxylase (ODC) activity and the incorporation of [<sup>3</sup>H]-thymidine into DNA. In addition, there was a significant reduction in histoarchitectural abnormalities such as epidermal thickness, number of epidermal cell layers, neutrophil infiltration, intercellular oedema, and vasodilation.</p><p><strong>Conclusion: </strong>Our results demonstrate that topical celecoxib can reduce the inflammation, hyperproliferation, and hyperplasiogenic events of skin insults suggesting that it may prove to be a valuable management option for cutaneous lesion and associated illnesses such as atopic dermatitis, eczema, and psoriasis, as well as the emergence of non-melanoma cancer.</p>","PeriodicalId":11023,"journal":{"name":"Cutaneous and Ocular Toxicology","volume":" ","pages":"87-96"},"PeriodicalIF":1.6,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138828689","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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