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Diagnostic utility of GDF15 in neurodegenerative diseases: A systematic review and meta‐analysis
INTRODUCTION: GDF15 may be a potential biomarker for neurodegenerative diseases. In this analysis, we aimed to quantitative analysis the levels of GDF15 in patients with neurological diseases and in health control, and then to determine its potential diagnostic utility. METHODS: Two researchers sepa...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8865151/ https://www.ncbi.nlm.nih.gov/pubmed/35068064 http://dx.doi.org/10.1002/brb3.2502 |
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author | Xue, Xin‐Hong Tao, Lin‐Lin Su, Dao‐Qing Guo, Cun‐Ju Liu, Hong |
author_facet | Xue, Xin‐Hong Tao, Lin‐Lin Su, Dao‐Qing Guo, Cun‐Ju Liu, Hong |
author_sort | Xue, Xin‐Hong |
collection | PubMed |
description | INTRODUCTION: GDF15 may be a potential biomarker for neurodegenerative diseases. In this analysis, we aimed to quantitative analysis the levels of GDF15 in patients with neurological diseases and in health control, and then to determine its potential diagnostic utility. METHODS: Two researchers separately conducted a systematic search of the relevant studies up to January 2021 in Embase, PubMed, and Web of Science. Effect sizes were estimated to use the standardized mean difference (SMD) with 95% confidence interval (CI). Sensitivity and specificity were calculated by the summary receiver operating characteristics curve (SROC) method. The sensitivity analysis was performed by the “one‐in/one‐out” approach. Considering the considerable heterogeneity among studies, random‐effects model was used for the meta‐analysis investigation. RESULTS: A total of eight articles were included in this meta‐analysis and systematic review. The pooled results of the random effect model indicated GDF15 levels were significantly higher in patients with neurodegenerative disease than healthy people (SMD = 0.92, 95% CI: 0.44–1.40, Z = 3.75, p < 0.001). Sensitivity and specificity of biomarker of GDF15 were 0.90 (95% CI: 0.75–0.97), 0.77 (95% CI: 0.67–0.65), and AUC = 0.87 (95% CI: 0.84–0.90), respectively. CONCLUSIONS: GDF15 levels were higher in patients with neurodegenerative disease than healthy people. And serum levels of GDF15 were a better marker for diagnostic utility of neurodegenerative disease. |
format | Online Article Text |
id | pubmed-8865151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88651512022-02-27 Diagnostic utility of GDF15 in neurodegenerative diseases: A systematic review and meta‐analysis Xue, Xin‐Hong Tao, Lin‐Lin Su, Dao‐Qing Guo, Cun‐Ju Liu, Hong Brain Behav Review INTRODUCTION: GDF15 may be a potential biomarker for neurodegenerative diseases. In this analysis, we aimed to quantitative analysis the levels of GDF15 in patients with neurological diseases and in health control, and then to determine its potential diagnostic utility. METHODS: Two researchers separately conducted a systematic search of the relevant studies up to January 2021 in Embase, PubMed, and Web of Science. Effect sizes were estimated to use the standardized mean difference (SMD) with 95% confidence interval (CI). Sensitivity and specificity were calculated by the summary receiver operating characteristics curve (SROC) method. The sensitivity analysis was performed by the “one‐in/one‐out” approach. Considering the considerable heterogeneity among studies, random‐effects model was used for the meta‐analysis investigation. RESULTS: A total of eight articles were included in this meta‐analysis and systematic review. The pooled results of the random effect model indicated GDF15 levels were significantly higher in patients with neurodegenerative disease than healthy people (SMD = 0.92, 95% CI: 0.44–1.40, Z = 3.75, p < 0.001). Sensitivity and specificity of biomarker of GDF15 were 0.90 (95% CI: 0.75–0.97), 0.77 (95% CI: 0.67–0.65), and AUC = 0.87 (95% CI: 0.84–0.90), respectively. CONCLUSIONS: GDF15 levels were higher in patients with neurodegenerative disease than healthy people. And serum levels of GDF15 were a better marker for diagnostic utility of neurodegenerative disease. John Wiley and Sons Inc. 2022-01-24 /pmc/articles/PMC8865151/ /pubmed/35068064 http://dx.doi.org/10.1002/brb3.2502 Text en © 2022 The Authors. Brain and Behavior published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Xue, Xin‐Hong Tao, Lin‐Lin Su, Dao‐Qing Guo, Cun‐Ju Liu, Hong Diagnostic utility of GDF15 in neurodegenerative diseases: A systematic review and meta‐analysis |
title | Diagnostic utility of GDF15 in neurodegenerative diseases: A systematic review and meta‐analysis |
title_full | Diagnostic utility of GDF15 in neurodegenerative diseases: A systematic review and meta‐analysis |
title_fullStr | Diagnostic utility of GDF15 in neurodegenerative diseases: A systematic review and meta‐analysis |
title_full_unstemmed | Diagnostic utility of GDF15 in neurodegenerative diseases: A systematic review and meta‐analysis |
title_short | Diagnostic utility of GDF15 in neurodegenerative diseases: A systematic review and meta‐analysis |
title_sort | diagnostic utility of gdf15 in neurodegenerative diseases: a systematic review and meta‐analysis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8865151/ https://www.ncbi.nlm.nih.gov/pubmed/35068064 http://dx.doi.org/10.1002/brb3.2502 |
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