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HMG-Coenzyme A Reductase as a Drug Target for the Prevention of Ankylosing Spondylitis
Statins are an inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGCR). Growing evidence indicates that statins may have an anti-inflammatory effect. Whether genetically proxied HMGCR inhibition can reduce the risk of ankylosing spondylitis is unknown. We constructed an HMGCR genetic sc...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8526849/ https://www.ncbi.nlm.nih.gov/pubmed/34692687 http://dx.doi.org/10.3389/fcell.2021.731072 |
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author | Zhong, Zhenyu Feng, Xiaojie Su, Guannan Du, Liping Liao, Weiting Liu, Shengyun Li, Fuzhen Zuo, Xianbo Yang, Peizeng |
author_facet | Zhong, Zhenyu Feng, Xiaojie Su, Guannan Du, Liping Liao, Weiting Liu, Shengyun Li, Fuzhen Zuo, Xianbo Yang, Peizeng |
author_sort | Zhong, Zhenyu |
collection | PubMed |
description | Statins are an inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGCR). Growing evidence indicates that statins may have an anti-inflammatory effect. Whether genetically proxied HMGCR inhibition can reduce the risk of ankylosing spondylitis is unknown. We constructed an HMGCR genetic score comprising nearly randomly inherited variants significantly associated with LDL cholesterol levels within ± 100 kb from HMGCR to proxy for inhibition of HMGCR. We also constructed PCSK9 and NPC1L1 scores as well as the LDL polygenetic score to proxy for the inhibition of these drug targets as well as serum LDL cholesterol levels, respectively. We then compared the associations of these genetic scores with the risk of ankylosing spondylitis. Of 33,998 participants in the primary cohort, 12,596 individuals had been diagnosed with ankylosing spondylitis. Genetically proxied inhibition of HMGCR scaled to per mmol/L decrease in LDL cholesterol levels by the HMGCR score was associated with a lower risk of ankylosing spondylitis (OR, 0.57; 95% CI, 0.38–0.85; P value = 5.7 × 10(–3)). No significant association with ankylosing spondylitis was observed for the PCSK9 score (OR, 0.89; 95% CI, 0.68–1.16) and the NPC1L1 score (OR, 1.50; 95% CI, 0.39–5.77). For the LDL score, genetically determined per mmol/L decrease in LDL cholesterol levels led to a reduced risk of ankylosing spondylitis (OR, 0.64; 95% CI, 0.43–0.94), with significant heterogeneity and pleiotropy in the estimate. Exploratory analyses showed that genetically proxied inhibition of HMGCR appeared to have a similar effect to long-term statin therapy in modifying the risk of coronary artery disease and type 2 diabetes, suggesting that the HMGCR score might be a reliable model to assess the effect of statin. Genetically proxied inhibition of HMGCR was associated with a decreased risk of ankylosing spondylitis. This mechanism-based estimate was in line with existing observations suggesting the clinical benefits of statin therapy for ankylosing spondylitis. |
format | Online Article Text |
id | pubmed-8526849 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85268492021-10-21 HMG-Coenzyme A Reductase as a Drug Target for the Prevention of Ankylosing Spondylitis Zhong, Zhenyu Feng, Xiaojie Su, Guannan Du, Liping Liao, Weiting Liu, Shengyun Li, Fuzhen Zuo, Xianbo Yang, Peizeng Front Cell Dev Biol Cell and Developmental Biology Statins are an inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGCR). Growing evidence indicates that statins may have an anti-inflammatory effect. Whether genetically proxied HMGCR inhibition can reduce the risk of ankylosing spondylitis is unknown. We constructed an HMGCR genetic score comprising nearly randomly inherited variants significantly associated with LDL cholesterol levels within ± 100 kb from HMGCR to proxy for inhibition of HMGCR. We also constructed PCSK9 and NPC1L1 scores as well as the LDL polygenetic score to proxy for the inhibition of these drug targets as well as serum LDL cholesterol levels, respectively. We then compared the associations of these genetic scores with the risk of ankylosing spondylitis. Of 33,998 participants in the primary cohort, 12,596 individuals had been diagnosed with ankylosing spondylitis. Genetically proxied inhibition of HMGCR scaled to per mmol/L decrease in LDL cholesterol levels by the HMGCR score was associated with a lower risk of ankylosing spondylitis (OR, 0.57; 95% CI, 0.38–0.85; P value = 5.7 × 10(–3)). No significant association with ankylosing spondylitis was observed for the PCSK9 score (OR, 0.89; 95% CI, 0.68–1.16) and the NPC1L1 score (OR, 1.50; 95% CI, 0.39–5.77). For the LDL score, genetically determined per mmol/L decrease in LDL cholesterol levels led to a reduced risk of ankylosing spondylitis (OR, 0.64; 95% CI, 0.43–0.94), with significant heterogeneity and pleiotropy in the estimate. Exploratory analyses showed that genetically proxied inhibition of HMGCR appeared to have a similar effect to long-term statin therapy in modifying the risk of coronary artery disease and type 2 diabetes, suggesting that the HMGCR score might be a reliable model to assess the effect of statin. Genetically proxied inhibition of HMGCR was associated with a decreased risk of ankylosing spondylitis. This mechanism-based estimate was in line with existing observations suggesting the clinical benefits of statin therapy for ankylosing spondylitis. Frontiers Media S.A. 2021-10-06 /pmc/articles/PMC8526849/ /pubmed/34692687 http://dx.doi.org/10.3389/fcell.2021.731072 Text en Copyright © 2021 Zhong, Feng, Su, Du, Liao, Liu, Li, Zuo and Yang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Zhong, Zhenyu Feng, Xiaojie Su, Guannan Du, Liping Liao, Weiting Liu, Shengyun Li, Fuzhen Zuo, Xianbo Yang, Peizeng HMG-Coenzyme A Reductase as a Drug Target for the Prevention of Ankylosing Spondylitis |
title | HMG-Coenzyme A Reductase as a Drug Target for the Prevention of Ankylosing Spondylitis |
title_full | HMG-Coenzyme A Reductase as a Drug Target for the Prevention of Ankylosing Spondylitis |
title_fullStr | HMG-Coenzyme A Reductase as a Drug Target for the Prevention of Ankylosing Spondylitis |
title_full_unstemmed | HMG-Coenzyme A Reductase as a Drug Target for the Prevention of Ankylosing Spondylitis |
title_short | HMG-Coenzyme A Reductase as a Drug Target for the Prevention of Ankylosing Spondylitis |
title_sort | hmg-coenzyme a reductase as a drug target for the prevention of ankylosing spondylitis |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8526849/ https://www.ncbi.nlm.nih.gov/pubmed/34692687 http://dx.doi.org/10.3389/fcell.2021.731072 |
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