5 results on '"Fahimeh Abdollahimajd"'
Search Results
2. Cutaneous adverse events related to COVID-19 vaccines: A cross-sectional questionnaire-based study of 867 patients
- Author
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Mehri Salari, Nastaran Namazi, Mohammad Shahidi Dadras, Reem Diab, Mohammad Reza Pourani, and Fahimeh Abdollahimajd
- Subjects
medicine.medical_specialty ,COVID-19 Vaccines ,Erythema ,Coronavirus disease 2019 (COVID-19) ,Population ,Dermatology ,Iran ,Surveys and Questionnaires ,Injection site reaction ,medicine ,Humans ,education ,Adverse effect ,education.field_of_study ,Angioedema ,business.industry ,SARS-CoV-2 ,Public health ,COVID-19 ,General Medicine ,medicine.disease ,Rash ,United States ,Cross-Sectional Studies ,medicine.symptom ,business - Abstract
Background Considering the emergency approval of the Food and Drug Administration for widespread use of coronavirus disease 2019 (COVID-19) vaccines, evaluating potential vaccine-related adverse effects is critical as it will allow physicians to diagnose and manage these complications properly. Methods In this descriptive cross-sectional questionnaire-based study, we evaluated the possible side effects of the COVID-19 vaccine from June 1, 2021, to June 21, 2021. The Iranian population is generally vaccinated with AstraZeneca, Sputnik V, Sinopharm, and Bharat vaccines. The continuous and categorical variables were described and data analyzed by the SPSS software version25. Results Cutaneous reactions occurred in 30% of individuals vaccinated against COVID-19. The most common cutaneous complications were focal injection site reaction, exanthematous rash, and urticaria. There were infrequent cutaneous adverse events that included vesicular eruption, pernio-like lesions, angioedema, erythema multiforme-like eruption, and zoster. Conclusion Acquainting physicians with COVID-19 vaccine-related cutaneous complications will assist them in detection and management. In addition, introducing these complications to individuals might improve acceptance of vaccine-related adverse effects in the general population.
- Published
- 2021
3. Metabolic syndrome in patients with Alopecia Areata: A case-control study
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Nastaran Namazi, Fahimeh Abdollahimajd, Nasim Niknezhad, Negin Bahreini, and Shima Younespour
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medicine.medical_specialty ,Alopecia Areata ,Dermatology ,030207 dermatology & venereal diseases ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,High-density lipoprotein ,medicine ,Prevalence ,Humans ,skin and connective tissue diseases ,Ophiasis ,Metabolic Syndrome ,integumentary system ,business.industry ,Alopecia totalis ,Case-control study ,General Medicine ,Alopecia areata ,medicine.disease ,chemistry ,030220 oncology & carcinogenesis ,Alopecia universalis ,Hair Disorder ,Case-Control Studies ,Metabolic syndrome ,business - Abstract
The aim of this study was to evaluate metabolic syndrome prevalence in patients with Alopecia Areata compared to controls. Sixty eligible patients with Alopecia Areata and 60 healthy subjects frequency matched for age and sex attending to our referral dermatology clinics from 2015 to 2017 were enrolled. Prevalence of metabolic syndrome and its components were compared between the two groups. Metabolic syndrome was only seen in seven patients (11.67%) and four controls (6.67%) without a significant difference (P = .34). The clinical presentations of AA included patch type (38.33%), ophiasis (6.67%), alopecia totalis (16.67%), and alopecia universalis (38.33%). Presence of metabolic syndrome was significantly associated with abdominal circumference (OR: 1.10, 95% CI for OR: 1.02to 1.19). Although there was no significant association between Alopecia Areata and metabolic syndrome, some components of metabolic syndrome were more prevalent in these patients. It may be concluded Alopecia Areata patients are at a higher risk of developing metabolic syndrome in the future. Further studies with larger sample sizes are needed.
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- 2021
4. The utility of dermal fibroblasts in treatment of skin disorders: A paradigm of recessive dystrophic epidermolysis bullosa
- Author
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Hamideh Moravvej, Simzar Hosseinzadeh, Forough Shams, Fahimeh Abdollahimajd, Hassan Vahidnezhad, Azam Rahimpour, Masoumeh Rajabibazl, Bahram Kazemi, and Jouni Uitto
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Collagen Type VII ,Cell ,Dermatology ,Skin Diseases ,Extracellular matrix ,Cell therapy ,Glycosaminoglycan ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,Dermis ,Medicine ,Humans ,Induced pluripotent stem cell ,Skin ,Wound Healing ,integumentary system ,business.industry ,Mesenchymal stem cell ,General Medicine ,Fibroblasts ,Epidermolysis Bullosa Dystrophica ,medicine.anatomical_structure ,030220 oncology & carcinogenesis ,Cancer research ,business ,Wound healing - Abstract
Dermal Fibroblasts are the most accessible cells in the skin that have gained significant attention in cell therapy. Applying dermal fibroblasts' regenerative capacity can introduce new patterns to develop cell-based therapies to treat skin disorders. Dermal fibroblasts originate from mesenchymal cells and are located within the dermis. These cells are mainly responsible for synthesizing glycosaminoglycans, collagens, and components of extracellular matrix (ECM) supporting skin's structural integrity. Preclinical studies suggested that allogeneic and autologous dermal fibroblasts provide widespread and beneficial applications for wound healing, burn ulcers, and inherited skin disorders. In this regard, generating induced pluripotent stem cells (iPSCs) from fibroblasts and gene-edited fibroblasts are promising approaches for treating skin disorders. Here, we aimed to review literature about ongoing and completed clinical trials that applied fibroblasts and bioengineered fibroblasts as therapeutic agents for various skin disorders. This review explores cell therapy protocols from the earliest phase of allogeneic and autologous fibroblasts development in different benches to translating them into bedside-level treatment for skin disorders, particularly recessive dystrophic epidermolysis bullosa (RDEB).
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- 2021
5. Neutrophil/platelet to lymphocyte ratio in monitoring of response to TNF-α inhibitors in psoriatic patients
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Niloofar Najar Nobari, Soheila Nasiri, Mehdi Gheisari, Fahimeh Abdollahimajd, and Mohammad Shahidi Dadras
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Blood Platelets ,medicine.medical_specialty ,Neutrophils ,Lymphocyte ,Inflammation ,Dermatology ,Gastroenterology ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,Psoriasis Area and Severity Index ,Internal medicine ,Psoriasis ,medicine ,Humans ,Platelet ,Lymphocytes ,Retrospective Studies ,business.industry ,Tumor Necrosis Factor-alpha ,fungi ,General Medicine ,medicine.disease ,Prognosis ,body regions ,medicine.anatomical_structure ,Tnf α inhibitors ,030220 oncology & carcinogenesis ,Alcohol intake ,Tumor Necrosis Factor Inhibitors ,medicine.symptom ,business ,Body mass index - Abstract
Neutrophil or platelet to lymphocyte ratio (NLR and PLR) has been proposed to be used as prognostic purposes in a variety of diseases. The aim of this study was to evaluate the usefulness of these ratios in monitoring of response to TNF-α-inhibitors in psoriatic patients. Eighty psoriatic patients were included and treated with TNF-α-inhibitors for 12 months based on drug protocol. Hematologic indices, including NLR and PLR values were assessed before and after treatment. Data on psoriasis area and severity index (PASI), smoking behavior, alcohol intake habit, nail abnormality, body mass index (BMI), joint involvement, and disease duration were also recorded. PASI scores were improved significantly after one-year treatment (P = .000). Furthermore, this type of treatment significantly reduced the NLR and PLR (P = .000). These changes were in accordance with PASI scores. Patients with BMI greater than 24.9 had higher, but non-significant NLR and PLR than normal or lean individuals. Cigarette smokers and alcohol consumers had lower NLR and PLR values than other individuals (P < .05). There was no significant association between NLR and PLR and joint or nail involvement. Although NLR and PLR will not be helpful in primary diagnosis of inflammatory diseases, they could be accounted as monitoring tools in management of psoriasis or globally indicators of inflammation.
- Published
- 2020
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