Muscle fiber-type distribution predicts weight gain and unfavourable left ventricular geometry: a 19 year follow-up study
dc.contributor.author | Karjalainen, Jouko | |
dc.contributor.author | Tikkanen, Heikki | |
dc.contributor.author | Hernelahti, Miika | |
dc.contributor.author | Kujala, Urho | |
dc.date.accessioned | 2011-05-13T07:31:28Z | |
dc.date.available | 2011-05-13T07:31:28Z | |
dc.date.issued | 2006 | |
dc.identifier.citation | Karjalainen, J., Tikkanen, H., Hernelahti, M. & Kujala, U. (2006). Muscle fiber-type distribution predicts weight gain and unfavourable left ventricular geometry: a 19 year follow-up study. BMC Cardiovascular Disorders, 6 (2). Retrieved from http://www.biomedcentral.com/1471-2261/6/2 | |
dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/26958 | |
dc.description.abstract | BACKGROUND: Skeletal muscle consists of type-I (slow-twitch) and type-II (fast-twitch) fibers, with proportions highly variable between individuals and mostly determined by genetic factors. Cross-sectional studies have associated low percentage of type-I fibers (type-I%) with many cardiovascular risk factors. METHODS: We investigated whether baseline type-I% predicts left ventricular (LV) structure and function at 19-year follow-up, and if so, which are the strongest mediating factors. At baseline in 1984 muscle fiber-type distribution (by actomyosin ATPase staining) was studied in 63 healthy men (aged 32–58 years). The follow-up in 2003 included echocardiography, measurement of obesity related variables, physical activity and blood pressure. RESULTS: In the 40 men not using cardiovascular drugs at follow-up, low type-I% predicted higher heart rate, blood pressure, and LV fractional shortening suggesting increased sympathetic tone. Low type-I% predicted smaller LV chamber diameters (P ≤ 0.009) and greater relative wall thickness (P = 0.034) without increase in LV mass (concentric remodeling). This was explained by the association of type-I% with obesity related variables. Type-I% was an independent predictor of follow-up body fat percentage, waist/hip ratio, weight gain in adulthood, and physical activity (in all P ≤ 0.001). After including these risk factors in the regression models, weight gain was the strongest predictor of LV geometry explaining 64% of the variation in LV end-diastolic diameter, 72% in end-systolic diameter, and 53% in relative wall thickness. CONCLUSION: Low type-I% predicts obesity and weight gain especially in the mid-abdomen, and consequently unfavourable LV geometry indicating increased cardiovascular risk. | en |
dc.language.iso | eng | |
dc.publisher | BioMed Central | |
dc.relation.ispartofseries | BMC Cardiovascular Disorders | |
dc.subject.other | lihassolu | en |
dc.subject.other | lihavuus | en |
dc.subject.other | sydän | en |
dc.subject.other | liikunta | en |
dc.subject.other | muscle fiber-type | en |
dc.subject.other | obesity | en |
dc.subject.other | heart | en |
dc.subject.other | physical activity | en |
dc.title | Muscle fiber-type distribution predicts weight gain and unfavourable left ventricular geometry: a 19 year follow-up study | |
dc.type | journal article | |
dc.identifier.urn | URN:NBN:fi:jyu-2011051310797 | |
dc.contributor.laitos | Terveystieteiden laitos | fi |
dc.contributor.laitos | Department of Health Sciences | en |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
dc.type.coar | http://purl.org/coar/resource_type/c_6501 | |
dc.description.reviewstatus | peerReviewed | |
dc.relation.issn | 1471-2261 | |
dc.type.version | publishedVersion | |
dc.rights.copyright | © 2006 Karjalainen et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. | |
dc.rights.accesslevel | openAccess | fi |
dc.type.publication | article | |
dc.rights.url | http://creativecommons.org/licenses/by/2 | |
dc.relation.doi | doi:10.1186/1471-2261-6-2 |
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Except where otherwise noted, this item's license is described as © 2006 Karjalainen et al; licensee BioMed Central Ltd.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.