98%
921
2 minutes
20
Importance: A comprehensive, user-friendly system to assess global ichthyosis disease burden is imperative to improving the care of patients with ichthyosis, identifying appropriate participants for clinical trials, and quantifying treatment outcomes. To our knowledge, there is currently no validated scale to objectively and systematically measure ichthyosis severity across the entire body.
Objective: To create and evaluate a comprehensive and user-friendly instrument to measure total body ichthyosis severity in adults and children.
Design, Setting, Participants: In this qualitative study, ichthyosis experts participated in the content development of the Ichthyosis Scoring System (ISS). The body was divided into 10 regions, and Likert scales (0-4) were created to quantify scale and erythema, with extensive descriptors and photographic standards. An 83-image teaching set was created from photographs of participants with ichthyosis. Two cohorts of dermatologists (11 total) independently scored all test photographs twice to evaluate interrater and intrarater reliabilities. Participants were enrolled worldwide from referral centers and patient advocacy groups. Participants of all ages, races, and ethnicities were included in the creation of ISS, and dermatologists with varying experience and areas of expertise participated as raters to evaluate the ISS. The study was conducted from 2019 to 2021, and the data were analyzed in 2021.
Main Outcomes And Measures: Intraclass correlation coefficients determined overall reliabilities.
Results: Across both cohorts of 11 dermatologists in total, the intraclass correlation coefficients for total, scale and erythema scores were greater than 0.90 (95% CI, 0.77-0.97), greater than 0.91 (95% CI, 0.79-0.98), and greater than 0.88 (95% CI, 0.72-0.97), respectively. Most body sites exhibited moderate to good interrater reliabilities for scale and erythema. Intrarater reliabilities were good to excellent.
Conclusions And Relevance: The results of this qualitative study demonstrate reproducibility and suggest that the ISS is a reliable system to measure global ichthyosis severity in adults and children.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8851366 | PMC |
http://dx.doi.org/10.1001/jamadermatol.2021.5917 | DOI Listing |
J Dermatol
September 2025
Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
A cross-sectional analysis was conducted to evaluate the impact of ichthyosis symptoms on the educational achievement and career choices of adults, or the potential future impact on children. A total of 77 respondents completed a questionnaire assessing the degree to which ichthyosis had impacted, or was expected to impact, their education and career. Responses were categorized as "none," "somewhat," or "greatly.
View Article and Find Full Text PDFJ Mother Child
February 2025
The University Hospital in Krakow, Malopolska, Poland.
Netherton syndrome (NS) is a rare, autosomal recessive genodermatosis resulting from mutations in the SPINK5 gene, which encodes the LEKTI (Lympho-Epithelial Kazal-type-related inhibitor) protein. This deficiency leads to dysregulated epidermal protease activity, primarily of kallikrein-related peptidases (KLKs), causing severe skin barrier defects, abnormal desquamation, and a complex immune dysregulation involving the T2 and T17 pathways. Clinically, NS is characterised by a triad of ichthyosiform erythroderma (often evolving from congenital ichthyosiform erythroderma to ichthyosis linearis circumflexa); pathognomonic hair shaft abnormalities, such as trichorrhexis invaginata ("bamboo hair"); and atopic manifestations with elevated serum IgE.
View Article and Find Full Text PDFBMC Pregnancy Childbirth
September 2025
Department of Pediatric Surgery, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Background: Adverse events during pregnancy are implicated in increasing the risk of congenital malformations in offspring. Current research does not fully encompass the spectrum of adverse events nor the mechanisms by which they affect fetal development.
Methods: A two-sample and two-step Mendelian randomization (MR) study was conducted to assess the association between adverse events during pregnancy and congenital malformations in offspring, and to investigate the mediating role of circulating metabolites in linking these adverse events to congenital malformations.
JAAD Int
October 2025
Department of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Background: Inherited ichthyoses (iI) are a heterogeneous group of keratinization disorders, whose microbiome composition and the role of dysbiosis remain largely unexplored.
Objectives: Characterization of the skin microbiome profile in iI and exploration of the significance of dysbiosis based on the literature.
Methods: A systematic search was performed across MEDLINE, Embase, Cochrane Library, Web of Science, and Scopus on 23 September 2024.
medRxiv
July 2025
University of Texas Health Science Center in San Antonio, San Antonio, TX, USA.
The X-linked Ichthyosis Follicularis, Alopecia, and Photophobia syndrome type 2 (IFAP2), is a condition that has been linked to an Arg527-to-Cys mutation in the gene. However, the molecular implications of the mutation in Meibomian glands remained unknown. Our goals were to elucidate the biochemical factors associated with the disease, and allow for unbiased diagnoses of the condition.
View Article and Find Full Text PDF