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Impact of Healthy Lifestyle in Patients With Familial Hypercholesterolemia
BACKGROUND: Pathogenic mutations are associated with poor outcomes in patients with familial hypercholesterolemia (FH). However, data on the effects of a healthy lifestyle on FH phenotypes are limited. OBJECTIVES: The authors investigated the interaction between a healthy lifestyle and FH mutation w...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9982286/ https://www.ncbi.nlm.nih.gov/pubmed/36873758 http://dx.doi.org/10.1016/j.jacasi.2022.10.012 |
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author | Tada, Hayato Kojima, Nobuko Yamagami, Kan Nomura, Akihiro Nohara, Atsushi Usui, Soichiro Sakata, Kenji Hayashi, Kenshi Fujino, Noboru Takamura, Masayuki Kawashiri, Masa-aki |
author_facet | Tada, Hayato Kojima, Nobuko Yamagami, Kan Nomura, Akihiro Nohara, Atsushi Usui, Soichiro Sakata, Kenji Hayashi, Kenshi Fujino, Noboru Takamura, Masayuki Kawashiri, Masa-aki |
author_sort | Tada, Hayato |
collection | PubMed |
description | BACKGROUND: Pathogenic mutations are associated with poor outcomes in patients with familial hypercholesterolemia (FH). However, data on the effects of a healthy lifestyle on FH phenotypes are limited. OBJECTIVES: The authors investigated the interaction between a healthy lifestyle and FH mutation with prognosis in patients with FH. METHODS: We investigated the associations of the interaction between genotypes and lifestyle, with the occurrence of major adverse cardiac events (MACE), such as cardiovascular-related mortality, myocardial infarction, unstable angina, and coronary artery revascularization, in patients with FH. We assessed their lifestyle based on 4 questionnaires (healthy dietary pattern, regular exercise, not smoking, and absence of obesity). The Cox proportional hazards model was used to assess the risk for MACE. RESULTS: The median follow-up duration was 12.6 (IQR: 9.5-17.9) years. During the follow-up duration, 179 MACE were observed. Independent of classic risk factors, FH mutation and lifestyle score were significantly associated with MACE (HR: 2.73; 95% CI: 1.03-4.43; P = 0.02; and HR: 0.69, 95% CI: 0.40-0.98, P = 0.033, respectively). The estimated risk of coronary artery disease by 75 years of age varied according to lifestyle, ranging from 21.0% among noncarriers with a favorable lifestyle to 32.1% among noncarriers with an unfavorable lifestyle and ranging from 29.0% among carriers with a favorable lifestyle to 55.4% among carriers with an unfavorable lifestyle. CONCLUSIONS: A healthy lifestyle was associated with reduced risk for MACE among patients with FH with or without genetic diagnosis. |
format | Online Article Text |
id | pubmed-9982286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-99822862023-03-04 Impact of Healthy Lifestyle in Patients With Familial Hypercholesterolemia Tada, Hayato Kojima, Nobuko Yamagami, Kan Nomura, Akihiro Nohara, Atsushi Usui, Soichiro Sakata, Kenji Hayashi, Kenshi Fujino, Noboru Takamura, Masayuki Kawashiri, Masa-aki JACC Asia Original Research BACKGROUND: Pathogenic mutations are associated with poor outcomes in patients with familial hypercholesterolemia (FH). However, data on the effects of a healthy lifestyle on FH phenotypes are limited. OBJECTIVES: The authors investigated the interaction between a healthy lifestyle and FH mutation with prognosis in patients with FH. METHODS: We investigated the associations of the interaction between genotypes and lifestyle, with the occurrence of major adverse cardiac events (MACE), such as cardiovascular-related mortality, myocardial infarction, unstable angina, and coronary artery revascularization, in patients with FH. We assessed their lifestyle based on 4 questionnaires (healthy dietary pattern, regular exercise, not smoking, and absence of obesity). The Cox proportional hazards model was used to assess the risk for MACE. RESULTS: The median follow-up duration was 12.6 (IQR: 9.5-17.9) years. During the follow-up duration, 179 MACE were observed. Independent of classic risk factors, FH mutation and lifestyle score were significantly associated with MACE (HR: 2.73; 95% CI: 1.03-4.43; P = 0.02; and HR: 0.69, 95% CI: 0.40-0.98, P = 0.033, respectively). The estimated risk of coronary artery disease by 75 years of age varied according to lifestyle, ranging from 21.0% among noncarriers with a favorable lifestyle to 32.1% among noncarriers with an unfavorable lifestyle and ranging from 29.0% among carriers with a favorable lifestyle to 55.4% among carriers with an unfavorable lifestyle. CONCLUSIONS: A healthy lifestyle was associated with reduced risk for MACE among patients with FH with or without genetic diagnosis. Elsevier 2023-01-31 /pmc/articles/PMC9982286/ /pubmed/36873758 http://dx.doi.org/10.1016/j.jacasi.2022.10.012 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Original Research Tada, Hayato Kojima, Nobuko Yamagami, Kan Nomura, Akihiro Nohara, Atsushi Usui, Soichiro Sakata, Kenji Hayashi, Kenshi Fujino, Noboru Takamura, Masayuki Kawashiri, Masa-aki Impact of Healthy Lifestyle in Patients With Familial Hypercholesterolemia |
title | Impact of Healthy Lifestyle in Patients With Familial Hypercholesterolemia |
title_full | Impact of Healthy Lifestyle in Patients With Familial Hypercholesterolemia |
title_fullStr | Impact of Healthy Lifestyle in Patients With Familial Hypercholesterolemia |
title_full_unstemmed | Impact of Healthy Lifestyle in Patients With Familial Hypercholesterolemia |
title_short | Impact of Healthy Lifestyle in Patients With Familial Hypercholesterolemia |
title_sort | impact of healthy lifestyle in patients with familial hypercholesterolemia |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9982286/ https://www.ncbi.nlm.nih.gov/pubmed/36873758 http://dx.doi.org/10.1016/j.jacasi.2022.10.012 |
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