4.7 Article

Multispectral raster-scanning optoacoustic mesoscopy differentiate lesional from non-lesional atopic dermatitis skin using structural and functional imaging markers

期刊

PHOTOACOUSTICS
卷 28, 期 -, 页码 -

出版社

ELSEVIER GMBH
DOI: 10.1016/j.pacs.2022.100399

关键词

Multispectral optoacoustic imaging; Atopic dermatitis; Oxygen saturation; Epidermis thickness; Total blood volume; Non-lesional atopic dermatitis

资金

  1. National Medical Research Council [NMRC OF-IRG, OFIRG18nov-0101]
  2. Agency for Science, Technology and Researchs (A*STAR) BMRC Central Research Fund
  3. iThera Medical as a part of the SBIC-iThera joint medical lab

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Atopic dermatitis is a chronic disease that significantly impacts healthcare management and patient quality of life. Using ms-RSOM imaging, we found a correlation between oxygen saturation and blood volume with clinical scoring for assessing the severity of AD. Additionally, we observed a relationship between epidermal thickness and disease severity.
Atopic dermatitis (AD) is a chronic and pruritic skin inflammatory disease causing a significant burden to health care management and patient's quality of life. Seemingly healthy skin or non-lesional sites on AD patients still presents skin barrier defects and immune response, which can develop to AD at a later stage. To investigate further the balance between the epidermal barrier impairment and intrinsic immune dysregulation in AD, we exploited multispectral Raster-Scanning Optoacoustic Mesoscopy (ms-RSOM) to image lesional and non-lesional skin areas on AD patients of different severities non-invasively to elucidate their structural features and functional information. Herein, we demonstrate the objective assessment of AD severity using relative changes in oxygen saturation (delta sO(2)) levels in microvasculature along with other structural parameters such as relative changes in epidermis thickness (delta ET) and total blood volume (8TBV) between the lesional and non-lesional areas of the skin. We could observe an increasing trend for delta sO(2) and delta TBV, which correlated well with the subjective clinical Scoring Atopic Dermatitis (SCORAD) for evaluating the severity. Notably, delta ET showed a decreasing trend with AD severity, indicating that the difference in epidermal thickness between lesional and non-lesional area of the skin decreases with AD severity. Our results also correlated well with conventional metrics such as trans-epidermal water loss (TEWL) and erythrosine sedimentation rate (ESR). We quantified the delta sO(2) and delta ET changes to objectively evaluate the treatment response before and four months after treatment using topical steroids and cyclosporine in one severe AD patient. We observed reduced delta sO(2) and delta ET post treatment. We envision that in future, functional and structural imaging metrics derived from ms-RSOM can be translated as objective markers to assess and stratify the severity of AD and understand the function of skin barrier dysfunctions and immune dysregulation. It could also be employed to monitor the treatment response of AD in regular clinical settings.

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