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Clinical utility of diagnostic guidelines and putative biomarkers in lymphangioleiomyomatosis

BACKGROUND: Lymphangioleiomyomatosis is a rare disease occurring almost exclusively in women. Diagnosis often requires surgical biopsy and the clinical course varies between patients with no predictors of progression. We evaluated recent diagnostic guidelines, clinical features and serum biomarkers...

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Autores principales: Chang, William YC, Cane, Jennifer L, Blakey, John D, Kumaran, Maruti, Pointon, Kate S, Johnson, Simon R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3431996/
https://www.ncbi.nlm.nih.gov/pubmed/22513045
http://dx.doi.org/10.1186/1465-9921-13-34
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author Chang, William YC
Cane, Jennifer L
Blakey, John D
Kumaran, Maruti
Pointon, Kate S
Johnson, Simon R
author_facet Chang, William YC
Cane, Jennifer L
Blakey, John D
Kumaran, Maruti
Pointon, Kate S
Johnson, Simon R
author_sort Chang, William YC
collection PubMed
description BACKGROUND: Lymphangioleiomyomatosis is a rare disease occurring almost exclusively in women. Diagnosis often requires surgical biopsy and the clinical course varies between patients with no predictors of progression. We evaluated recent diagnostic guidelines, clinical features and serum biomarkers as diagnostic and prognostic tools. METHODS: Serum vascular endothelial growth factor-D (VEGF-D), angiotensin converting enzyme (ACE), matrix metalloproteinases (MMP) -2 and -9, clinical phenotype, thoracic and abdominal computerised tomography, lung function and quality of life were examined in a cohort of 58 patients. 32 healthy female controls had serum biomarkers measured. RESULTS: Serum VEGF-D, ACE and total MMP-2 levels were elevated in patients. VEGF-D was the strongest discriminator between patients and controls (median = 1174 vs. 332 pg/ml p < 0.0001 with an area under the receiver operating characteristic curve of 0.967, 95% CI 0.93-1.01). Application of European Respiratory Society criteria allowed a definite diagnosis without biopsy in 69%. Adding VEGF-D measurement to ERS criteria further reduced the need for biopsy by 10%. VEGF-D was associated with lymphatic involvement (p = 0.017) but not the presence of angiomyolipomas. CONCLUSIONS: Combining ERS criteria and serum VEGF-D reduces the need for lung biopsy in LAM. VEGF-D was associated with lymphatic disease but not lung function.
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spelling pubmed-34319962012-09-01 Clinical utility of diagnostic guidelines and putative biomarkers in lymphangioleiomyomatosis Chang, William YC Cane, Jennifer L Blakey, John D Kumaran, Maruti Pointon, Kate S Johnson, Simon R Respir Res Research BACKGROUND: Lymphangioleiomyomatosis is a rare disease occurring almost exclusively in women. Diagnosis often requires surgical biopsy and the clinical course varies between patients with no predictors of progression. We evaluated recent diagnostic guidelines, clinical features and serum biomarkers as diagnostic and prognostic tools. METHODS: Serum vascular endothelial growth factor-D (VEGF-D), angiotensin converting enzyme (ACE), matrix metalloproteinases (MMP) -2 and -9, clinical phenotype, thoracic and abdominal computerised tomography, lung function and quality of life were examined in a cohort of 58 patients. 32 healthy female controls had serum biomarkers measured. RESULTS: Serum VEGF-D, ACE and total MMP-2 levels were elevated in patients. VEGF-D was the strongest discriminator between patients and controls (median = 1174 vs. 332 pg/ml p < 0.0001 with an area under the receiver operating characteristic curve of 0.967, 95% CI 0.93-1.01). Application of European Respiratory Society criteria allowed a definite diagnosis without biopsy in 69%. Adding VEGF-D measurement to ERS criteria further reduced the need for biopsy by 10%. VEGF-D was associated with lymphatic involvement (p = 0.017) but not the presence of angiomyolipomas. CONCLUSIONS: Combining ERS criteria and serum VEGF-D reduces the need for lung biopsy in LAM. VEGF-D was associated with lymphatic disease but not lung function. BioMed Central 2012 2012-04-18 /pmc/articles/PMC3431996/ /pubmed/22513045 http://dx.doi.org/10.1186/1465-9921-13-34 Text en Copyright ©2012 Chang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Chang, William YC
Cane, Jennifer L
Blakey, John D
Kumaran, Maruti
Pointon, Kate S
Johnson, Simon R
Clinical utility of diagnostic guidelines and putative biomarkers in lymphangioleiomyomatosis
title Clinical utility of diagnostic guidelines and putative biomarkers in lymphangioleiomyomatosis
title_full Clinical utility of diagnostic guidelines and putative biomarkers in lymphangioleiomyomatosis
title_fullStr Clinical utility of diagnostic guidelines and putative biomarkers in lymphangioleiomyomatosis
title_full_unstemmed Clinical utility of diagnostic guidelines and putative biomarkers in lymphangioleiomyomatosis
title_short Clinical utility of diagnostic guidelines and putative biomarkers in lymphangioleiomyomatosis
title_sort clinical utility of diagnostic guidelines and putative biomarkers in lymphangioleiomyomatosis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3431996/
https://www.ncbi.nlm.nih.gov/pubmed/22513045
http://dx.doi.org/10.1186/1465-9921-13-34
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