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Non-invasive intradermal imaging of cystine crystals in cystinosis

IMPORTANCE: Development of noninvasive methodology to reproducibly measure tissue cystine crystal load to assess disease status and guide clinical care in cystinosis, an inherited lysosomal storage disorder characterized by widespread cystine crystal accumulation. OBJECTIVE: To develop an unbiased a...

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Autores principales: Bengali, Marya, Goodman, Spencer, Sun, Xiaoying, Dohil, Magdalene A., Dohil, Ranjan, Newbury, Robert, Lobry, Tatiana, Hernandez, Laura, Antignac, Corinne, Jain, Sonia, Cherqui, Stephanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7932553/
https://www.ncbi.nlm.nih.gov/pubmed/33661986
http://dx.doi.org/10.1371/journal.pone.0247846
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author Bengali, Marya
Goodman, Spencer
Sun, Xiaoying
Dohil, Magdalene A.
Dohil, Ranjan
Newbury, Robert
Lobry, Tatiana
Hernandez, Laura
Antignac, Corinne
Jain, Sonia
Cherqui, Stephanie
author_facet Bengali, Marya
Goodman, Spencer
Sun, Xiaoying
Dohil, Magdalene A.
Dohil, Ranjan
Newbury, Robert
Lobry, Tatiana
Hernandez, Laura
Antignac, Corinne
Jain, Sonia
Cherqui, Stephanie
author_sort Bengali, Marya
collection PubMed
description IMPORTANCE: Development of noninvasive methodology to reproducibly measure tissue cystine crystal load to assess disease status and guide clinical care in cystinosis, an inherited lysosomal storage disorder characterized by widespread cystine crystal accumulation. OBJECTIVE: To develop an unbiased and semi-automated imaging methodology to quantify dermal cystine crystal accumulation in patients to correlate with disease status. DESIGN, SETTING AND PARTICIPANTS: 101 participants, 70 patients and 31 healthy controls, were enrolled at the University of California, San Diego, Cystinosis Clinics, Rady Children’s Hospital, San Diego and at the annual Cystinosis Research Foundation family conference for an ongoing prospective longitudinal cohort study of cystinosis patients with potential yearly follow-up. EXPOSURES: Intradermal reflectance confocal microscopy (RCM) imaging, blood collection via standard venipuncture, medical record collection, and occasional skin punch biopsies. MAIN OUTCOMES AND MEASURES: The primary outcome was to establish an automated measure of normalized confocal crystal volume (nCCV) for each subject. Secondary analysis examined the association of nCCV with various clinical indicators to assess nCCV’s possible predictive potential. RESULTS: Over 2 years, 57 patients diagnosed with cystinosis (median [range] age: 15.1 yrs [0.8, 54]; 41.4% female) were intradermally assessed by RCM to produce 84 image stacks. 27 healthy individuals (38.7 yrs [10, 85]; 53.1% female) were also imaged providing 37 control image stacks. Automated 2D crystal area quantification revealed that patients had significantly elevated crystal accumulation within the superficial dermis. 3D volumetric analysis of this region was significantly higher in patients compared to healthy controls (mean [SD]: 1934.0 μm(3) [1169.1] for patients vs. 363.1 μm(3) [194.3] for controls, P<0.001). Medical outcome data was collected from 43 patients with infantile cystinosis (media [range] age: 11 yrs [0.8, 54]; 51% female). nCCV was positively associated with hypothyroidism (OR = 19.68, 95% CI: [1.60, 242.46], P = 0.02) and stage of chronic kidney disease (slope estimate = 0.53, 95%CI: [0.05, 1.00], P = 0.03). CONCLUSIONS AND RELEVANCE: This study used non-invasive RCM imaging to develop an intradermal cystine crystal quantification method. Results showed that cystinosis patients had increased nCCV compared to healthy controls. Level of patient nCCV correlated with several clinical outcomes suggesting nCCV may be used as a potential new biomarker for cystinosis to monitor long-term disease control and medication compliance.
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spelling pubmed-79325532021-03-15 Non-invasive intradermal imaging of cystine crystals in cystinosis Bengali, Marya Goodman, Spencer Sun, Xiaoying Dohil, Magdalene A. Dohil, Ranjan Newbury, Robert Lobry, Tatiana Hernandez, Laura Antignac, Corinne Jain, Sonia Cherqui, Stephanie PLoS One Research Article IMPORTANCE: Development of noninvasive methodology to reproducibly measure tissue cystine crystal load to assess disease status and guide clinical care in cystinosis, an inherited lysosomal storage disorder characterized by widespread cystine crystal accumulation. OBJECTIVE: To develop an unbiased and semi-automated imaging methodology to quantify dermal cystine crystal accumulation in patients to correlate with disease status. DESIGN, SETTING AND PARTICIPANTS: 101 participants, 70 patients and 31 healthy controls, were enrolled at the University of California, San Diego, Cystinosis Clinics, Rady Children’s Hospital, San Diego and at the annual Cystinosis Research Foundation family conference for an ongoing prospective longitudinal cohort study of cystinosis patients with potential yearly follow-up. EXPOSURES: Intradermal reflectance confocal microscopy (RCM) imaging, blood collection via standard venipuncture, medical record collection, and occasional skin punch biopsies. MAIN OUTCOMES AND MEASURES: The primary outcome was to establish an automated measure of normalized confocal crystal volume (nCCV) for each subject. Secondary analysis examined the association of nCCV with various clinical indicators to assess nCCV’s possible predictive potential. RESULTS: Over 2 years, 57 patients diagnosed with cystinosis (median [range] age: 15.1 yrs [0.8, 54]; 41.4% female) were intradermally assessed by RCM to produce 84 image stacks. 27 healthy individuals (38.7 yrs [10, 85]; 53.1% female) were also imaged providing 37 control image stacks. Automated 2D crystal area quantification revealed that patients had significantly elevated crystal accumulation within the superficial dermis. 3D volumetric analysis of this region was significantly higher in patients compared to healthy controls (mean [SD]: 1934.0 μm(3) [1169.1] for patients vs. 363.1 μm(3) [194.3] for controls, P<0.001). Medical outcome data was collected from 43 patients with infantile cystinosis (media [range] age: 11 yrs [0.8, 54]; 51% female). nCCV was positively associated with hypothyroidism (OR = 19.68, 95% CI: [1.60, 242.46], P = 0.02) and stage of chronic kidney disease (slope estimate = 0.53, 95%CI: [0.05, 1.00], P = 0.03). CONCLUSIONS AND RELEVANCE: This study used non-invasive RCM imaging to develop an intradermal cystine crystal quantification method. Results showed that cystinosis patients had increased nCCV compared to healthy controls. Level of patient nCCV correlated with several clinical outcomes suggesting nCCV may be used as a potential new biomarker for cystinosis to monitor long-term disease control and medication compliance. Public Library of Science 2021-03-04 /pmc/articles/PMC7932553/ /pubmed/33661986 http://dx.doi.org/10.1371/journal.pone.0247846 Text en © 2021 Bengali et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Bengali, Marya
Goodman, Spencer
Sun, Xiaoying
Dohil, Magdalene A.
Dohil, Ranjan
Newbury, Robert
Lobry, Tatiana
Hernandez, Laura
Antignac, Corinne
Jain, Sonia
Cherqui, Stephanie
Non-invasive intradermal imaging of cystine crystals in cystinosis
title Non-invasive intradermal imaging of cystine crystals in cystinosis
title_full Non-invasive intradermal imaging of cystine crystals in cystinosis
title_fullStr Non-invasive intradermal imaging of cystine crystals in cystinosis
title_full_unstemmed Non-invasive intradermal imaging of cystine crystals in cystinosis
title_short Non-invasive intradermal imaging of cystine crystals in cystinosis
title_sort non-invasive intradermal imaging of cystine crystals in cystinosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7932553/
https://www.ncbi.nlm.nih.gov/pubmed/33661986
http://dx.doi.org/10.1371/journal.pone.0247846
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