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Platelet distribution width as a novel indicator of disease activity in systemic lupus erythematosus
BACKGROUND: Significance of platelet distribution width (PDW) and mean platelet volume (MPV) in assessing disease activity of systemic lupus erythematosus (SLE) remains unclear. This study was aimed to evaluate PDW and MPV as potential disease activity markers in adult SLE patients. MATERIALS AND ME...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5996572/ https://www.ncbi.nlm.nih.gov/pubmed/29937910 http://dx.doi.org/10.4103/jrms.JRMS_1038_16 |
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author | Chen, Sun-Yi Du, Juan Lu, Xiao-Nian Xu, Jin-Hua |
author_facet | Chen, Sun-Yi Du, Juan Lu, Xiao-Nian Xu, Jin-Hua |
author_sort | Chen, Sun-Yi |
collection | PubMed |
description | BACKGROUND: Significance of platelet distribution width (PDW) and mean platelet volume (MPV) in assessing disease activity of systemic lupus erythematosus (SLE) remains unclear. This study was aimed to evaluate PDW and MPV as potential disease activity markers in adult SLE patients. MATERIALS AND METHODS: A total of 204 study participants, including 91 SLE patients and 113 age- and gender-matched healthy controls, were selected in this cross-sectional study. They were classified into three groups: control group (n = 113), active SLE group (n = 54), and inactive SLE group (n = 37). Demographic, clinical, and laboratory data were analyzed. RESULTS: In patient group, PDW was statistically higher than that in control group (13.54 ± 2.67 vs. 12.65 ± 2.34, P = 0.012), and in active group, PDW was significantly increased compared to inactive group (14.31 ± 2.90 vs. 12.25 ± 1.55, P < 0.001). However, MPV was significantly lower in SLE group than in control group (10.74 ± 0.94 vs. 11.09 ± 1.14, P = 0.016). PDW was positively correlated with SLE disease activity index (P < 0.001, r = 0.529) and erythrocyte sedimentation rate (P = 0.002, r = 0.321) and negatively correlated with C3 (P < 0.001, r = −0.419). However, there was no significant association between MPV and these study variables. A PDW level of 11.85% was determined as a predictive cutoff value of SLE diagnosis (sensitivity 76.9%, specificity 42.5%) and 13.65% as cutoff of active stage (sensitivity 52.6%, specificity 85.3%). CONCLUSION: This study first associates a higher PDW level with an increased SLE activity, suggesting PDW as a novel indicator to monitor the activity of SLE. |
format | Online Article Text |
id | pubmed-5996572 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59965722018-06-22 Platelet distribution width as a novel indicator of disease activity in systemic lupus erythematosus Chen, Sun-Yi Du, Juan Lu, Xiao-Nian Xu, Jin-Hua J Res Med Sci Original Article BACKGROUND: Significance of platelet distribution width (PDW) and mean platelet volume (MPV) in assessing disease activity of systemic lupus erythematosus (SLE) remains unclear. This study was aimed to evaluate PDW and MPV as potential disease activity markers in adult SLE patients. MATERIALS AND METHODS: A total of 204 study participants, including 91 SLE patients and 113 age- and gender-matched healthy controls, were selected in this cross-sectional study. They were classified into three groups: control group (n = 113), active SLE group (n = 54), and inactive SLE group (n = 37). Demographic, clinical, and laboratory data were analyzed. RESULTS: In patient group, PDW was statistically higher than that in control group (13.54 ± 2.67 vs. 12.65 ± 2.34, P = 0.012), and in active group, PDW was significantly increased compared to inactive group (14.31 ± 2.90 vs. 12.25 ± 1.55, P < 0.001). However, MPV was significantly lower in SLE group than in control group (10.74 ± 0.94 vs. 11.09 ± 1.14, P = 0.016). PDW was positively correlated with SLE disease activity index (P < 0.001, r = 0.529) and erythrocyte sedimentation rate (P = 0.002, r = 0.321) and negatively correlated with C3 (P < 0.001, r = −0.419). However, there was no significant association between MPV and these study variables. A PDW level of 11.85% was determined as a predictive cutoff value of SLE diagnosis (sensitivity 76.9%, specificity 42.5%) and 13.65% as cutoff of active stage (sensitivity 52.6%, specificity 85.3%). CONCLUSION: This study first associates a higher PDW level with an increased SLE activity, suggesting PDW as a novel indicator to monitor the activity of SLE. Medknow Publications & Media Pvt Ltd 2018-05-30 /pmc/articles/PMC5996572/ /pubmed/29937910 http://dx.doi.org/10.4103/jrms.JRMS_1038_16 Text en Copyright: © 2018 Journal of Research in Medical Sciences http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Chen, Sun-Yi Du, Juan Lu, Xiao-Nian Xu, Jin-Hua Platelet distribution width as a novel indicator of disease activity in systemic lupus erythematosus |
title | Platelet distribution width as a novel indicator of disease activity in systemic lupus erythematosus |
title_full | Platelet distribution width as a novel indicator of disease activity in systemic lupus erythematosus |
title_fullStr | Platelet distribution width as a novel indicator of disease activity in systemic lupus erythematosus |
title_full_unstemmed | Platelet distribution width as a novel indicator of disease activity in systemic lupus erythematosus |
title_short | Platelet distribution width as a novel indicator of disease activity in systemic lupus erythematosus |
title_sort | platelet distribution width as a novel indicator of disease activity in systemic lupus erythematosus |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5996572/ https://www.ncbi.nlm.nih.gov/pubmed/29937910 http://dx.doi.org/10.4103/jrms.JRMS_1038_16 |
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