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1.
Clin Exp Dermatol ; 46(7): 1277-1284, 2021 Oct.
Article in English | MEDLINE | ID: mdl-33969517

ABSTRACT

BACKGROUND: Prurigo nodularis (PN) is a chronic inflammatory skin disease characterized by intense pruritus, but information on patient experience and impact on quality of life (QoL) remains understudied. AIM: To characterize disease characteristics and QoL in a global sample of patients with PN. METHODS: An anonymous survey was distributed via patient support groups for PN. RESULTS: In total, 231 members responded to the survey. The majority of respondents reported itch localized both to nodules and to intervening skin (67.0%). Associated symptoms included prickling, pain, stinging and burning. The extensor lower legs (69% right, 67.3% left) and flexor forearms (66.1% right, 62% left) were the most common sites of itch. Participants reported frequent healthcare utilization, with 36.3% visiting a doctor ≥ 10 times in the past year. Physician-diagnosed anxiety (45.4%), depression (16.4%) and the atopic triad (18.7%) were commonly reported. Patients with PN had mean scores of 16.4, 11.6 and 16.8 on the Dermatology Life Quality Index, Pittsburgh Sleep Quality Index and 5-Dimensions Itch, respectively. CONCLUSIONS: Severe pruritus with accompanying pain, stinging and burning is characteristic of PN, with the majority of patients experiencing itch in both nodular and interlesional skin. Patients further report decreased QoL scores and impaired sleep. Patient experiences should guide future management of PN.


Subject(s)
Cost of Illness , Prurigo , Pruritus/etiology , Quality of Life , Adult , Anxiety/epidemiology , Anxiety/etiology , Female , Health Surveys , Humans , Male , Middle Aged , Patient Acceptance of Health Care/statistics & numerical data , Patient Reported Outcome Measures , Prurigo/complications , Prurigo/psychology , Pruritus/epidemiology , United States/epidemiology
3.
Clin Exp Dermatol ; 46(7): 1236-1242, 2021 Oct.
Article in English | MEDLINE | ID: mdl-33763852

ABSTRACT

BACKGROUND: Prurigo nodularis (PN) is associated with a variety of systemic comorbidities, including infectious diseases such as HIV and viral hepatitis. There are limited data on other infectious disease comorbidities in patients with PN. AIM: To characterize infectious disease hospitalizations among patients with PN and the associated cost burden. METHODS: We searched the 2016-2017 National Inpatient Sample, a cross-sectional sample of 20% of all US hospitalizations, for infectious disease hospitalizations among patients with PN. Associations of PN with infections and related costs were determined using multivariable logistic and linear regression, adjusting for age, race, sex and insurance type. RESULTS: PN was associated with any infection overall (OR = 2.98, 95% CI 2.49-3.56), and with HIV, cutaneous, hepatobiliary, central nervous system, bacterial, viral and fungal/parasitic infections and for sepsis. Patients with PN had a higher mean cost of care (US$11 667 vs. US$8893, P < 0.001) and length of stay (5.5 vs. 4.2 days, P < 0.001) for any infection overall and for 7 of 13 other infections. Adjusting for age, race, sex and insurance coverage, PN was associated with higher cost (+30%, 95% CI +17 to +44%) and higher length of stay (+30%, 95% CI +18 to +44%) for any infection overall, and for several specific infections. These associations remained with alternate regression models adjusting for severity of illness. CONCLUSION: There is a high infectious disease burden among patients with PN, corresponding to higher healthcare utilization and spending. Clinicians must be aware of these associations when treating these patients with immunomodulatory drugs.


Subject(s)
Communicable Diseases/complications , Hospitalization/statistics & numerical data , Prurigo/complications , Cross-Sectional Studies , Female , Health Care Costs , Humans , Length of Stay , Linear Models , Male , Prurigo/ethnology , Psoriasis
4.
Clin Exp Dermatol ; 46(5): 820-824, 2021 Jul.
Article in English | MEDLINE | ID: mdl-33484582

ABSTRACT

Atopic dermatitis (AD) is chronic, pruritic, inflammatory skin disease that affects a significant portion of the population in industrialized nations. For nonresponders to conventional therapies, AD can significantly reduce sleep quality and quality of life. AD pathogenesis is multifactorial and involves multiple immune pathways, with recent evidence of T helper (Th)2, Th17 and Th22 axis attenuation in various AD endotypes and racial subtypes. Inhibition of the conserved Janus kinase (JAK) signalling pathway represents a promising therapeutic avenue to reduce the activation of multiple proinflammatory mediators involved in AD pathogenesis. JAK inhibitors exist in both oral and topical forms with variable specificity for the receptor tyrosine kinases JAK1, JAK2, JAK3 and tyrosine kinase 2. Oral formulations include abrocitinib, upadacitinib, baricitinib and gusacitinib, and are most appropriate for patients with moderate to severe AD. Emerging topical formulation in development include ruxolitinib and deglocitinib, which may be used in patients with localized AD and also adjunctively with systemic therapy in patients with more severe disease. With observed rapidity in itch relief and accompanying dramatic reduction in inflammatory lesion count, JAK inhibitors represent a promising new treatment to revolutionize the management of AD.


Subject(s)
Dermatitis, Atopic/drug therapy , Dermatitis, Atopic/immunology , Janus Kinase Inhibitors/pharmacology , Janus Kinase Inhibitors/therapeutic use , Acetonitriles/administration & dosage , Acetonitriles/pharmacology , Acetonitriles/therapeutic use , Administration, Oral , Administration, Topical , Adult , Azetidines/administration & dosage , Azetidines/pharmacology , Azetidines/therapeutic use , Child , Dermatitis, Atopic/physiopathology , Dermatitis, Atopic/psychology , Heterocyclic Compounds, 3-Ring/administration & dosage , Heterocyclic Compounds, 3-Ring/pharmacology , Heterocyclic Compounds, 3-Ring/therapeutic use , Humans , Janus Kinase 1/antagonists & inhibitors , Janus Kinase 2/antagonists & inhibitors , Janus Kinase 3/antagonists & inhibitors , Janus Kinase Inhibitors/administration & dosage , Nitriles/administration & dosage , Nitriles/pharmacology , Nitriles/therapeutic use , Piperidines/administration & dosage , Piperidines/pharmacology , Piperidines/therapeutic use , Purines/administration & dosage , Purines/pharmacology , Purines/therapeutic use , Pyrazoles/administration & dosage , Pyrazoles/pharmacology , Pyrazoles/therapeutic use , Pyridazines/administration & dosage , Pyridazines/pharmacology , Pyridazines/therapeutic use , Pyrimidines/administration & dosage , Pyrimidines/pharmacology , Pyrimidines/therapeutic use , Quality of Life , STAT1 Transcription Factor/pharmacology , Safety , Severity of Illness Index , Sulfonamides/administration & dosage , Sulfonamides/pharmacology , Sulfonamides/therapeutic use , TYK2 Kinase/antagonists & inhibitors , Treatment Outcome
5.
Int J Cosmet Sci ; 40(2): 157-164, 2018 Apr.
Article in English | MEDLINE | ID: mdl-29369367

ABSTRACT

OBJECTIVE: This research examines the benefits of caffeine absorption on hair stiffness. To test hair stiffness, we have developed an evaluation method that is not only accurate, but also inexpensive. Our evaluation method for measuring hair stiffness culminated in a model, called the Stiffness-Angle Law, which describes the elastic properties of hair and can be widely applied to the development of hair care products. METHODS: Small molecules (≤500 g mol-1 ) such as caffeine can be absorbed into hair. A common shampoo containing 4% caffeine was formulated and applied to hair 10 times, after which the hair stiffness was measured. The caffeine absorption of the treated hair was observed using Fourier-transform infrared spectroscopy (FTIR) with a focal plane array (FPA) detector. Our evaluation method for measuring hair stiffness consists of a regular camera and a support for single strands of hair. After attaching the hair to the support, the bending angle of the hair was observed with a camera and measured. Then, the hair strand was weighed. The stiffness of the hair was calculated based on our proposed Stiffness-Angle Law using three variables: angle, weight of hair and the distance the hair was pulled across the support. RESULTS: The caffeine absorption was confirmed by FTIR analysis. The concentration of amide bond in the hair certainly increased due to caffeine absorption. After caffeine was absorbed into the hair, the bending angle and weight of the hair changed. Applying these measured changes to the Stiffness-Angle Law, it was confirmed that the hair stiffness increased by 13.2% due to caffeine absorption. CONCLUSION: The theoretical results using the Stiffness-Angle Law agree with the visual examinations of hair exposed to caffeine and also the known results of hair stiffness from a previous report. Our evaluation method combined with our proposed Stiffness-Angle Law effectively provides an accurate and inexpensive evaluation technique for measuring bending stiffness of human hair.


Subject(s)
Caffeine/metabolism , Hair , Caffeine/chemistry , Humans , Molecular Weight , Spectroscopy, Fourier Transform Infrared
6.
Arch Pathol Lab Med ; 120(1): 86-9, 1996 Jan.
Article in English | MEDLINE | ID: mdl-8554452

ABSTRACT

Fabry's disease is a rare, inherited, X-linked metabolic storage disease with ceramide hexoside due to alpha-galactosidase A deficiency. Patients with typical Fabry's disease usually present with several clinical manifestations of corneal dystrophy, neurologic abnormalities, cardiovascular disease, heavy proteinuria, and characteristic cutaneous angiokeratoma. However, atypical Fabry's disease with oligosymptomatic phenotype presents with symptoms restricted solely to cardiocytes or kidney and might be diagnosed by chance during a routine endomyocardial or renal biopsy examination. In this article, we report a case of Fabry's disease incidentally diagnosed in a 34-year-old man who presented with intermittent trace or 1(+) proteinuria only. This patient had no history of renal disease in any other family member. A renal biopsy to evaluate trace proteinuria revealed histologic and ultrastructural findings compatible with Fabry's disease. Subsequent to the renal biopsy, a skin biopsy on a few initially unrecognized, scattered, dark-pinkish scrotal papules showed typical angiokeratoma. A biochemical enzymatic assay of alpha-galactosidase in urine and plasma revealed a markedly decreased enzyme level in the hemizygous range.


Subject(s)
Fabry Disease/pathology , Adult , Fabry Disease/blood , Fabry Disease/classification , Fabry Disease/urine , Fluorescent Antibody Technique , Humans , Kidney Diseases/blood , Kidney Diseases/diagnosis , Kidney Diseases/urine , Male , Proteinuria/blood , Proteinuria/diagnosis , Proteinuria/urine , Skin Diseases/blood , Skin Diseases/diagnosis , Skin Diseases/urine , alpha-Galactosidase/blood , alpha-Galactosidase/urine
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