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Assessing the role of blood pressure in amyotrophic lateral sclerosis: a Mendelian randomization study
BACKGROUND: Observational studies have suggested a close but controversial relationship between blood pressure (BP) and amyotrophic lateral sclerosis (ALS). It remains unclear whether this association is causal. The authors employed a bidirectional two-sample Mendelian randomization (MR) approach to...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8848798/ https://www.ncbi.nlm.nih.gov/pubmed/35172853 http://dx.doi.org/10.1186/s13023-022-02212-0 |
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author | Xia, Kailin Zhang, Linjing Tang, Lu Huang, Tao Fan, Dongsheng |
author_facet | Xia, Kailin Zhang, Linjing Tang, Lu Huang, Tao Fan, Dongsheng |
author_sort | Xia, Kailin |
collection | PubMed |
description | BACKGROUND: Observational studies have suggested a close but controversial relationship between blood pressure (BP) and amyotrophic lateral sclerosis (ALS). It remains unclear whether this association is causal. The authors employed a bidirectional two-sample Mendelian randomization (MR) approach to evaluate the causal relationship between BP and ALS. Genetic proxies for systolic blood pressure (SBP), diastolic blood pressure (DBP), antihypertensive drugs (AHDs), ALS, and their corresponding genome-wide association study (GWAS) summary datasets were obtained from the most recent studies with the largest sample sizes. The inverse variance weighted (IVW) method was adopted as the main approach to examine the effect of BP on ALS and four other MR methods were used for sensitivity analyses. To exclude the interference between SBP and DBP, a multivariable MR approach was used. RESULTS: We found that genetically determined increased DBP was a protective factor for ALS (OR = 0.978, 95% CI 0.960–0.996, P = 0.017) and that increased SBP was an independent risk factor for ALS (OR = 1.014, 95% CI 1.003–1.025, P = 0.015), which is supported by sensitivity analyses. The use of calcium channel blocker (CCB) showed a causal relationship with ALS (OR = 0.985, 95% CI 0.971–1.000, P = 0.049). No evidence was revealed that ALS caused changes in BP. CONCLUSIONS: This study provides genetic support for a causal effect of BP and ALS that increased DBP has a protective effect on ALS, and increased SBP is a risk factor for ALS, which may be related to sympathetic excitability. Blood pressure management is essential in ALS, and CCB may be a promising candidate. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-022-02212-0. |
format | Online Article Text |
id | pubmed-8848798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88487982022-02-18 Assessing the role of blood pressure in amyotrophic lateral sclerosis: a Mendelian randomization study Xia, Kailin Zhang, Linjing Tang, Lu Huang, Tao Fan, Dongsheng Orphanet J Rare Dis Research BACKGROUND: Observational studies have suggested a close but controversial relationship between blood pressure (BP) and amyotrophic lateral sclerosis (ALS). It remains unclear whether this association is causal. The authors employed a bidirectional two-sample Mendelian randomization (MR) approach to evaluate the causal relationship between BP and ALS. Genetic proxies for systolic blood pressure (SBP), diastolic blood pressure (DBP), antihypertensive drugs (AHDs), ALS, and their corresponding genome-wide association study (GWAS) summary datasets were obtained from the most recent studies with the largest sample sizes. The inverse variance weighted (IVW) method was adopted as the main approach to examine the effect of BP on ALS and four other MR methods were used for sensitivity analyses. To exclude the interference between SBP and DBP, a multivariable MR approach was used. RESULTS: We found that genetically determined increased DBP was a protective factor for ALS (OR = 0.978, 95% CI 0.960–0.996, P = 0.017) and that increased SBP was an independent risk factor for ALS (OR = 1.014, 95% CI 1.003–1.025, P = 0.015), which is supported by sensitivity analyses. The use of calcium channel blocker (CCB) showed a causal relationship with ALS (OR = 0.985, 95% CI 0.971–1.000, P = 0.049). No evidence was revealed that ALS caused changes in BP. CONCLUSIONS: This study provides genetic support for a causal effect of BP and ALS that increased DBP has a protective effect on ALS, and increased SBP is a risk factor for ALS, which may be related to sympathetic excitability. Blood pressure management is essential in ALS, and CCB may be a promising candidate. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-022-02212-0. BioMed Central 2022-02-16 /pmc/articles/PMC8848798/ /pubmed/35172853 http://dx.doi.org/10.1186/s13023-022-02212-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Xia, Kailin Zhang, Linjing Tang, Lu Huang, Tao Fan, Dongsheng Assessing the role of blood pressure in amyotrophic lateral sclerosis: a Mendelian randomization study |
title | Assessing the role of blood pressure in amyotrophic lateral sclerosis: a Mendelian randomization study |
title_full | Assessing the role of blood pressure in amyotrophic lateral sclerosis: a Mendelian randomization study |
title_fullStr | Assessing the role of blood pressure in amyotrophic lateral sclerosis: a Mendelian randomization study |
title_full_unstemmed | Assessing the role of blood pressure in amyotrophic lateral sclerosis: a Mendelian randomization study |
title_short | Assessing the role of blood pressure in amyotrophic lateral sclerosis: a Mendelian randomization study |
title_sort | assessing the role of blood pressure in amyotrophic lateral sclerosis: a mendelian randomization study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8848798/ https://www.ncbi.nlm.nih.gov/pubmed/35172853 http://dx.doi.org/10.1186/s13023-022-02212-0 |
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