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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...

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Autores principales: Xue, Xin‐Hong, Tao, Lin‐Lin, Su, Dao‐Qing, Guo, Cun‐Ju, Liu, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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.
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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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