Pub Date : 2025-11-01DOI: 10.25259/IJDVL_1027_2024
Abhishek R Parekh, Hiral A Shah
Blood donation is an act of benevolence that significantly improves lives and fosters better health outcomes globally. Certain skin diseases and medications make an individual temporarily or permanently ineligible to donate blood. This article aims to elucidate the relationship between skin diseases, medication, and blood donation deferral periods, empowering individuals to make informed decisions and contribute to this life-saving endeavour.
{"title":"Blood donation and dermatology: What a dermatologist should know?","authors":"Abhishek R Parekh, Hiral A Shah","doi":"10.25259/IJDVL_1027_2024","DOIUrl":"10.25259/IJDVL_1027_2024","url":null,"abstract":"<p><p>Blood donation is an act of benevolence that significantly improves lives and fosters better health outcomes globally. Certain skin diseases and medications make an individual temporarily or permanently ineligible to donate blood. This article aims to elucidate the relationship between skin diseases, medication, and blood donation deferral periods, empowering individuals to make informed decisions and contribute to this life-saving endeavour.</p>","PeriodicalId":50376,"journal":{"name":"Indian Journal of Dermatology Venereology & Leprology","volume":" ","pages":"752-759"},"PeriodicalIF":3.4,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142781728","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}
Pub Date : 2025-11-01DOI: 10.25259/IJDVL_1755_2024
Wenjun Lin, Fengchuan Zhang, Shuying Lv, Ying Wang, Dingquan Yang
Background Alopecia areata (AA) is a chronic autoimmune dermatosis with significant challenges in the treatment of severe cases. Recently, tofacitinib has been a promising cure for moderate to severe AA. Yet, its long-term efficacy and safety in the treatment of alopecia totalis (AT) and alopecia universalis (AU) remain underexplored, and determinants of its effectiveness are poorly understood. Aim To evaluate the long-term efficacy and safety of tofacitinib in AT and AU patients and explore the factors that may influence treatment outcomes. Methods We retrospectively assessed the efficacy and safety of tofacitinib in 69 AT and AU patients between January 2020 and June 2024. We also explored risk factors affecting the efficacy of tofacitinib using binary logistic regression analysis. Results After a median treatment of 6 months with tofacitinib, 47.8% (33/69) of patients had a severity of alopecia tool (SALT) score ≤ 20, and 26.1% (18/69) had complete hair regrowth. Patients showed more pronounced SALT score reductions and significant efficacy at weeks 24 and 36, compared to week 12 (P < 0.01). Binary logistic regression analysis revealed that younger initial age of AA (odds ratio (OR) = 1.063, 95% confidence interval (CI) 1.011-1.117, P = 0.017) and shorter treatment duration (OR = 1.249, 95% CI 1.065-1.465, P = 0.006) were significant risk factors associated with poorer efficacy of tofacitinib. Acneiform rash and folliculitis were the primary adverse effects. Limitation The single-center, retrospective study may be limited by data deficiencies and a small sample size. Conclusion Tofacitinib demonstrated significant efficacy in treating patients with AT and AU within a minimum of 6 months. Severe adverse reactions were not observed. Notably, the age of AA onset and the duration of tofacitinib treatment may be significant factors influencing its therapeutic outcomes.
背景斑秃(AA)是一种慢性自身免疫性皮肤病,严重病例的治疗具有重大挑战。最近,托法替尼已成为一种有希望的治疗中度至重度AA的方法。然而,其治疗全面性脱发(AT)和普遍性脱发(AU)的长期疗效和安全性仍未得到充分探讨,其有效性的决定因素也知之甚少。目的评价托法替尼治疗AT和AU患者的长期疗效和安全性,探讨可能影响治疗结果的因素。方法回顾性评估2020年1月至2024年6月期间69例AT和AU患者使用托法替尼的疗效和安全性。我们还利用二元logistic回归分析探讨了影响托法替尼疗效的危险因素。结果托法替尼治疗6个月后,47.8%(33/69)患者的脱发工具严重程度评分≤20分,26.1%(18/69)患者的头发完全再生。与第12周相比,患者在第24周和第36周表现出更明显的SALT评分下降和显著的疗效(P < 0.01)。二元logistic回归分析显示,AA初始年龄较小(优势比(OR) = 1.063, 95%可信区间(CI) 1.011 ~ 1.117, P = 0.017)和治疗时间较短(OR = 1.249, 95% CI 1.065 ~ 1.465, P = 0.006)是托法替尼疗效较差的显著危险因素。痤疮样皮疹和毛囊炎是主要的不良反应。单中心、回顾性研究可能受到数据不足和样本量小的限制。结论托法替尼治疗AT和AU患者至少6个月的疗效显著。未见严重不良反应。值得注意的是,AA的发病年龄和托法替尼治疗的持续时间可能是影响其治疗结果的重要因素。
{"title":"Efficacy and safety of tofacitinib in patients with total and universal alopecia- A retrospective evaluation of 69 patients.","authors":"Wenjun Lin, Fengchuan Zhang, Shuying Lv, Ying Wang, Dingquan Yang","doi":"10.25259/IJDVL_1755_2024","DOIUrl":"10.25259/IJDVL_1755_2024","url":null,"abstract":"<p><p>Background Alopecia areata (AA) is a chronic autoimmune dermatosis with significant challenges in the treatment of severe cases. Recently, tofacitinib has been a promising cure for moderate to severe AA. Yet, its long-term efficacy and safety in the treatment of alopecia totalis (AT) and alopecia universalis (AU) remain underexplored, and determinants of its effectiveness are poorly understood. Aim To evaluate the long-term efficacy and safety of tofacitinib in AT and AU patients and explore the factors that may influence treatment outcomes. Methods We retrospectively assessed the efficacy and safety of tofacitinib in 69 AT and AU patients between January 2020 and June 2024. We also explored risk factors affecting the efficacy of tofacitinib using binary logistic regression analysis. Results After a median treatment of 6 months with tofacitinib, 47.8% (33/69) of patients had a severity of alopecia tool (SALT) score ≤ 20, and 26.1% (18/69) had complete hair regrowth. Patients showed more pronounced SALT score reductions and significant efficacy at weeks 24 and 36, compared to week 12 (P < 0.01). Binary logistic regression analysis revealed that younger initial age of AA (odds ratio (OR) = 1.063, 95% confidence interval (CI) 1.011-1.117, P = 0.017) and shorter treatment duration (OR = 1.249, 95% CI 1.065-1.465, P = 0.006) were significant risk factors associated with poorer efficacy of tofacitinib. Acneiform rash and folliculitis were the primary adverse effects. Limitation The single-center, retrospective study may be limited by data deficiencies and a small sample size. Conclusion Tofacitinib demonstrated significant efficacy in treating patients with AT and AU within a minimum of 6 months. Severe adverse reactions were not observed. Notably, the age of AA onset and the duration of tofacitinib treatment may be significant factors influencing its therapeutic outcomes.</p>","PeriodicalId":50376,"journal":{"name":"Indian Journal of Dermatology Venereology & Leprology","volume":" ","pages":"771-775"},"PeriodicalIF":3.4,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144056532","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}
{"title":"Patches and petals: A terracotta interpretation of vitiligo.","authors":"Shivangi Arora","doi":"10.25259/IJDVL_962_2025","DOIUrl":"10.25259/IJDVL_962_2025","url":null,"abstract":"","PeriodicalId":50376,"journal":{"name":"Indian Journal of Dermatology Venereology & Leprology","volume":" ","pages":"845"},"PeriodicalIF":3.4,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144876608","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}
Pub Date : 2025-11-01DOI: 10.25259/IJDVL_1385_2024
Agata Karny, Miłosz Nesterowicz, Julia Nowowiejska, Piotr Purpurowicz, Anna Baran, Tomasz W Kaminski, Zbigniew Purpurowicz, Iwona Flisiak
Background Acne vulgaris is one of the most common cutaneous chronic diseases. The disease itself or the side effects of medications can play a crucial role in the development of sexual dysfunction. Aim Assessment of the occurrence of sexual dysfunction in female patients with acne vulgaris. Methods The study included 82 women diagnosed with acne vulgaris and 133 female controls without skin diseases. The sexual health of the subjects was assessed using the Female Sexual Function Index (FSFI) via an online anonymous questionnaire. Additional information regarding patients' medical history was analysed. Results There was no statistically significant difference in the total FSFI score between patients and controls (p > 0.05). Patients had significantly higher scores than controls in the satisfaction domain (p < 0.05). There was a positive correlation between the question about the subjective effect of skin condition on sexual desire and the likelihood of sexual dysfunction in the FSFI (p < 0.05, r = 0.33). Patients using retinoids had a slightly reduced FSFI (p = 0.44), which correlated negatively with retinoid use (p = 0.0428, r = -0.4257). Women receiving oral retinoids had downward trends in the satisfaction and pain domains (p = 0.41 and p = 0.198, respectively). Retinoid treatment was negatively correlated with the overall FSFI lubrication domain score (p = 0.0423, r = -0.4268). In addition, there was also a negative correlation between retinoid therapy and the overall FSFI orgasm domain score (p = 0.0024, r = -0.6014). Limitations The inability to evaluate the severity of acne vulgaris; the relatively small sample size; no matching of cases and controls with respect to age; and the lack of physician-confirmed data regarding the effectiveness of the administered treatment. Conclusions Some female patients with acne vulgaris may be at higher risk of sexual dysfunction. Decreased self-esteem and the general psychological burden of this dermatosis may negatively influence sexual functioning, so it is important to pay attention to this aspect. Patients who need help in this area should be referred to appropriate specialists.
寻常痤疮是最常见的皮肤慢性疾病之一。疾病本身或药物的副作用在性功能障碍的发展中起着至关重要的作用。目的探讨女性寻常性痤疮患者性功能障碍的发生情况。方法选取诊断为寻常性痤疮的女性患者82例,对照组133例无皮肤病。使用女性性功能指数(FSFI)通过在线匿名问卷对受试者的性健康进行评估。分析了有关患者病史的其他信息。结果患者与对照组FSFI总分比较,差异无统计学意义(p < 0.05)。患者满意度得分显著高于对照组(p < 0.05)。在FSFI中,皮肤状况对性欲的主观影响问题与性功能障碍可能性呈正相关(p < 0.05, r = 0.33)。使用类维甲酸的患者FSFI略有降低(p = 0.44),与类维甲酸的使用呈负相关(p = 0.0428, r = -0.4257)。口服类维生素a的女性在满意度和疼痛方面呈下降趋势(p = 0.41和p = 0.198)。类维甲酸治疗与FSFI润滑域总分呈负相关(p = 0.0423, r = -0.4268)。此外,类维甲酸治疗与FSFI高潮域总分呈负相关(p = 0.0024, r = -0.6014)。局限性:不能评价寻常痤疮的严重程度;样本量相对较小;病例和对照在年龄方面没有匹配;以及缺乏医生证实的治疗有效性的数据。结论部分女性寻常性痤疮患者存在较高的性功能障碍风险。自尊心下降和这种皮肤病的一般心理负担可能会对性功能产生负面影响,因此注意这方面是很重要的。在这方面需要帮助的患者应转介给适当的专家。
{"title":"Sexual dysfunction in female patients with acne vulgaris - A questionnaire-based survey.","authors":"Agata Karny, Miłosz Nesterowicz, Julia Nowowiejska, Piotr Purpurowicz, Anna Baran, Tomasz W Kaminski, Zbigniew Purpurowicz, Iwona Flisiak","doi":"10.25259/IJDVL_1385_2024","DOIUrl":"10.25259/IJDVL_1385_2024","url":null,"abstract":"<p><p>Background Acne vulgaris is one of the most common cutaneous chronic diseases. The disease itself or the side effects of medications can play a crucial role in the development of sexual dysfunction. Aim Assessment of the occurrence of sexual dysfunction in female patients with acne vulgaris. Methods The study included 82 women diagnosed with acne vulgaris and 133 female controls without skin diseases. The sexual health of the subjects was assessed using the Female Sexual Function Index (FSFI) via an online anonymous questionnaire. Additional information regarding patients' medical history was analysed. Results There was no statistically significant difference in the total FSFI score between patients and controls (p > 0.05). Patients had significantly higher scores than controls in the satisfaction domain (p < 0.05). There was a positive correlation between the question about the subjective effect of skin condition on sexual desire and the likelihood of sexual dysfunction in the FSFI (p < 0.05, r = 0.33). Patients using retinoids had a slightly reduced FSFI (p = 0.44), which correlated negatively with retinoid use (p = 0.0428, r = -0.4257). Women receiving oral retinoids had downward trends in the satisfaction and pain domains (p = 0.41 and p = 0.198, respectively). Retinoid treatment was negatively correlated with the overall FSFI lubrication domain score (p = 0.0423, r = -0.4268). In addition, there was also a negative correlation between retinoid therapy and the overall FSFI orgasm domain score (p = 0.0024, r = -0.6014). Limitations The inability to evaluate the severity of acne vulgaris; the relatively small sample size; no matching of cases and controls with respect to age; and the lack of physician-confirmed data regarding the effectiveness of the administered treatment. Conclusions Some female patients with acne vulgaris may be at higher risk of sexual dysfunction. Decreased self-esteem and the general psychological burden of this dermatosis may negatively influence sexual functioning, so it is important to pay attention to this aspect. Patients who need help in this area should be referred to appropriate specialists.</p>","PeriodicalId":50376,"journal":{"name":"Indian Journal of Dermatology Venereology & Leprology","volume":" ","pages":"783-787"},"PeriodicalIF":3.4,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144876514","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}
Pub Date : 2025-11-01DOI: 10.25259/IJDVL_1165_2023
Gabriela Danessa, Dion Notario, Regina Regina
Background Ageing is a degenerative process that affects the entire body. Skin ageing is characterised by a decrease in the levels of collagen, elastin fibre, and hyaluronic acid (HA), resulting in a loss of skin elasticity and hydration. Prior studies suggest that oral collagen supplements can help increase collagen, elastin, and HA levels, ultimately improving skin health. Objective To assess the impact of collagen-based supplements on the signs of skin ageing and determine the effective dosage. Methods This systematic review and meta-analysis utilized PubMed, Clinical Key, ProQuest, and Cochrane Library databases to identify studies published from 2010 to 2021. It includes ten randomised controlled trials (RCTs) with a total of 646 participants. Results The findings indicate that collagen supplements were statistically effective in increasing skin hydration (SMD 1.25 (CI: 0.77-1.74)) and elasticity (SMD 0.61 (CI: 0.21-1.02)). The most commonly administered dose was 4 g/day, with a median dose of 3.5 g/ day. Limitations Most of the studies could not control for weather-related factors. The findings are more applicable to females. Moderate heterogeneity (I2 = 55.5-56.5%) may limit generalisability. The risk of bias was generally unclear, and publication bias could not be assessed due to the small number of studies. Conclusion Oral administration of collagen supplement in a dose ranging from 1-10 g/day was statistically effective in increasing the skin hydration and elasticity.
{"title":"Effects of collagen-based supplements on skin's hydration and elasticity: A systematic review and meta-analysis.","authors":"Gabriela Danessa, Dion Notario, Regina Regina","doi":"10.25259/IJDVL_1165_2023","DOIUrl":"10.25259/IJDVL_1165_2023","url":null,"abstract":"<p><p>Background Ageing is a degenerative process that affects the entire body. Skin ageing is characterised by a decrease in the levels of collagen, elastin fibre, and hyaluronic acid (HA), resulting in a loss of skin elasticity and hydration. Prior studies suggest that oral collagen supplements can help increase collagen, elastin, and HA levels, ultimately improving skin health. Objective To assess the impact of collagen-based supplements on the signs of skin ageing and determine the effective dosage. Methods This systematic review and meta-analysis utilized PubMed, Clinical Key, ProQuest, and Cochrane Library databases to identify studies published from 2010 to 2021. It includes ten randomised controlled trials (RCTs) with a total of 646 participants. Results The findings indicate that collagen supplements were statistically effective in increasing skin hydration (SMD 1.25 (CI: 0.77-1.74)) and elasticity (SMD 0.61 (CI: 0.21-1.02)). The most commonly administered dose was 4 g/day, with a median dose of 3.5 g/ day. Limitations Most of the studies could not control for weather-related factors. The findings are more applicable to females. Moderate heterogeneity (I2 = 55.5-56.5%) may limit generalisability. The risk of bias was generally unclear, and publication bias could not be assessed due to the small number of studies. Conclusion Oral administration of collagen supplement in a dose ranging from 1-10 g/day was statistically effective in increasing the skin hydration and elasticity.</p>","PeriodicalId":50376,"journal":{"name":"Indian Journal of Dermatology Venereology & Leprology","volume":" ","pages":"730-740"},"PeriodicalIF":3.4,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144876589","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}
{"title":"Multi drug failure of tinea corporis to terbinafine, itraconazole and fluconazole; translating extensive Indian microbiological and resistance data to a trial of ketoconazole with remarkable efficacy.","authors":"Savitha Sharath, Kabir Sardana, Ananta Khurana","doi":"10.25259/IJDVL_497_2024","DOIUrl":"10.25259/IJDVL_497_2024","url":null,"abstract":"","PeriodicalId":50376,"journal":{"name":"Indian Journal of Dermatology Venereology & Leprology","volume":" ","pages":"807-809"},"PeriodicalIF":3.4,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141996850","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}
Pub Date : 2025-11-01DOI: 10.25259/IJDVL_1541_2024
Ihab Younis, Nehad Ahmed Fouad, Ola Salah Ibrahim, Karem Taha Khalil
Background The exact mechanisms underlying the eradication of the human papillomavirus (HPV) by cellular immunity remain obscure. Individuals with treatment-resistant warts frequently have immune deficiencies. Amino-peptidases (ERAP1, ERAP2) of the endoplasmic reticulum are essential for the production of antigenic epitopes that attach to the Major Histocompatibility Complex (MHC) class I and activate T-lymphocytes or natural killer (NK) cells. Aim To assess ERAP1 and ERAP2 serum concentrations in patients with resistant warts. Methods The current study included 200 subjects. They were split into 2 groups. Group (I) patients had resistant warts (n = 100), and group (II) age- and sex-matched subjects had a history of treated warts with no recurrence (n = 100). Clinical assessment and ERAP1 and ERAP2 serum level determination via ELISA were conducted. Results ERAP1 and ERAP2 levels were significantly lower in group (I) than in group (II) (p < 0.0001 for each). A significant positive relationship was observed between ERAP1 and ERAP2 (p < 0.001). A significant negative correlation was found between ERAP1, ERAP2, the number of warts, and a number of recurrences (p < 0.001). Limitations The small sample size, the lack of measurements of ERAP1 and ERAP2 before and after the treatment, and the exclusion of medical conditions such as diabetes mellitus and hypertension. Conclusion The current study findings highlight the potential utility of serum ERAP1 and ERAP2 as novel biomarkers for identifying patients with recalcitrant warts.
{"title":"Utility of serum ERAP1 and ERAP2 as novel biomarkers in the management of recalcitrant warts: A cross-sectional study.","authors":"Ihab Younis, Nehad Ahmed Fouad, Ola Salah Ibrahim, Karem Taha Khalil","doi":"10.25259/IJDVL_1541_2024","DOIUrl":"10.25259/IJDVL_1541_2024","url":null,"abstract":"<p><p>Background The exact mechanisms underlying the eradication of the human papillomavirus (HPV) by cellular immunity remain obscure. Individuals with treatment-resistant warts frequently have immune deficiencies. Amino-peptidases (ERAP1, ERAP2) of the endoplasmic reticulum are essential for the production of antigenic epitopes that attach to the Major Histocompatibility Complex (MHC) class I and activate T-lymphocytes or natural killer (NK) cells. Aim To assess ERAP1 and ERAP2 serum concentrations in patients with resistant warts. Methods The current study included 200 subjects. They were split into 2 groups. Group (I) patients had resistant warts (n = 100), and group (II) age- and sex-matched subjects had a history of treated warts with no recurrence (n = 100). Clinical assessment and ERAP1 and ERAP2 serum level determination via ELISA were conducted. Results ERAP1 and ERAP2 levels were significantly lower in group (I) than in group (II) (p < 0.0001 for each). A significant positive relationship was observed between ERAP1 and ERAP2 (p < 0.001). A significant negative correlation was found between ERAP1, ERAP2, the number of warts, and a number of recurrences (p < 0.001). Limitations The small sample size, the lack of measurements of ERAP1 and ERAP2 before and after the treatment, and the exclusion of medical conditions such as diabetes mellitus and hypertension. Conclusion The current study findings highlight the potential utility of serum ERAP1 and ERAP2 as novel biomarkers for identifying patients with recalcitrant warts.</p>","PeriodicalId":50376,"journal":{"name":"Indian Journal of Dermatology Venereology & Leprology","volume":" ","pages":"725-729"},"PeriodicalIF":3.4,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144530874","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}