Iris Pigmented Lesions: Unraveling the Genetic Basis of Iris Freckles and Nevi
Julia Boldu-Roig, Elena Sorli-Clemente, Aida Kuljuh-Causevic, Alba Loras, Alfonso Anton, Conrado Martinez-Cadenas

TL;DR
This study explores the genetic and demographic factors behind iris freckles and nevi in a Spanish population, linking them to pigmentation genes and traits like eye color and age.
Contribution
The study identifies specific genetic associations with iris freckles and nevi, particularly highlighting IRF4 and sex-specific effects.
Findings
Iris freckles and nevi are linked to IRF4, HERC2, OCA2, and SLC45A2 genes, especially in females.
Iris nevi are associated with IRF4, HERC2, and TYR in brown-eyed individuals.
MC1R, a key gene for skin freckles, is not associated with iris freckles or nevi.
Abstract
To investigate the diversity of pigmented benign lesions in the human iris, aiming to provide insights for forensic, biomedical, and ophthalmological research. A cohort of 1014 individuals of Spanish descent was analyzed. Digital slit-lamp photographs were used to evaluate iris pigmentation traits, including iris freckles, iris nevi, iris color, and the presence of a pigmented collarette. A candidate gene association study was performed on these pigmentation traits. Both iris freckles and nevi were associated with increased age, female sex, pigmented collarette, and eye color (mainly green). Additionally, higher freckle and nevus counts were observed in participants with more facial freckles and cutaneous nevi and were positively associated with each other. After adjustment, a positive significant association was identified between the presence of iris freckles and genetic variants in…
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
Topicsmelanin and skin pigmentation · RNA regulation and disease · Cutaneous Melanoma Detection and Management
