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The effect of vitamin K1 on arterial calcification activity in subjects with diabetes mellitus: a post hoc analysis of a double-blind, randomized, placebo-controlled trial
Coronary and aortic artery calcifications are generally slow to develop, and their burden predicts cardiovascular disease events. In patients with diabetes mellitus, arterial calcification is accelerated and calcification activity can be detected using 18F-sodium fluoride positron emission tomograph...
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Published in: | The American journal of clinical nutrition 2022-01, Vol.115 (1), p.45-52 |
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creator | Bellinge, Jamie W Francis, Roslyn J Lee, Sing C Bondonno, Nicola P Sim, Marc Lewis, Joshua R Watts, Gerald F Schultz, Carl J |
description | Coronary and aortic artery calcifications are generally slow to develop, and their burden predicts cardiovascular disease events. In patients with diabetes mellitus, arterial calcification is accelerated and calcification activity can be detected using 18F-sodium fluoride positron emission tomography (18F-NaF PET).
We aimed to determine whether vitamin K1 supplementation inhibits arterial calcification activity in individuals with diabetes mellitus.
This was a post hoc analysis of the ViKCoVaC (effect of Vitamin-K1 and Colchicine on Vascular Calcification activity in subjects with Diabetes Mellitus) double-blind randomized controlled trial conducted in Perth, Western Australia. Individuals with diabetes mellitus and established coronary calcification (coronary calcium score > 10), but without clinical coronary artery disease, underwent baseline 18F-NaF PET imaging, followed by oral vitamin K1 supplementation (10 mg/d) or placebo for 3 mo, after which 18F-NaF PET imaging was repeated. We tested whether individuals randomly assigned to vitamin K1 supplementation had reduced development of new 18F-NaF PET positive lesions within the coronary arteries and aorta.
In total, 149 individuals completed baseline and follow-up imaging studies. Vitamin K1 supplementation independently decreased the odds of developing new 18F-NaF PET positive lesions in the coronary arteries (OR: 0.35; 95% CI: 0.16, 0.78; P = 0.010), aorta (OR: 0.27; 95% CI: 0.08, 0.94; P = 0.040), and in both aortic and coronary arteries (OR: 0.28; 95% CI: 0.13, 0.63; P = 0.002).
In individuals with diabetes mellitus, supplementation with 10 mg vitamin K1/d may prevent the development of newly calcifying lesions within the aorta and the coronary arteries as detected using 18F-NaF PET. Further long-term studies are needed to test this hypothesis.
This trial was registered at anzctr.org.au as ACTRN12616000024448.
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doi_str_mv | 10.1093/ajcn/nqab306 |
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We aimed to determine whether vitamin K1 supplementation inhibits arterial calcification activity in individuals with diabetes mellitus.
This was a post hoc analysis of the ViKCoVaC (effect of Vitamin-K1 and Colchicine on Vascular Calcification activity in subjects with Diabetes Mellitus) double-blind randomized controlled trial conducted in Perth, Western Australia. Individuals with diabetes mellitus and established coronary calcification (coronary calcium score > 10), but without clinical coronary artery disease, underwent baseline 18F-NaF PET imaging, followed by oral vitamin K1 supplementation (10 mg/d) or placebo for 3 mo, after which 18F-NaF PET imaging was repeated. We tested whether individuals randomly assigned to vitamin K1 supplementation had reduced development of new 18F-NaF PET positive lesions within the coronary arteries and aorta.
In total, 149 individuals completed baseline and follow-up imaging studies. Vitamin K1 supplementation independently decreased the odds of developing new 18F-NaF PET positive lesions in the coronary arteries (OR: 0.35; 95% CI: 0.16, 0.78; P = 0.010), aorta (OR: 0.27; 95% CI: 0.08, 0.94; P = 0.040), and in both aortic and coronary arteries (OR: 0.28; 95% CI: 0.13, 0.63; P = 0.002).
In individuals with diabetes mellitus, supplementation with 10 mg vitamin K1/d may prevent the development of newly calcifying lesions within the aorta and the coronary arteries as detected using 18F-NaF PET. Further long-term studies are needed to test this hypothesis.
This trial was registered at anzctr.org.au as ACTRN12616000024448.
▪</description><identifier>ISSN: 0002-9165</identifier><identifier>EISSN: 1938-3207</identifier><identifier>DOI: 10.1093/ajcn/nqab306</identifier><identifier>PMID: 34637494</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aged ; Aorta ; Aorta - diagnostic imaging ; aortic diseases ; arterial calcification ; Arteries ; Arteriosclerosis ; Calcification ; Calcification (ectopic) ; Cardiovascular disease ; Cardiovascular diseases ; Clinical trials ; Colchicine ; Coronary artery ; Coronary artery disease ; Coronary vessels ; Coronary Vessels - diagnostic imaging ; Diabetes ; Diabetes mellitus ; Diabetes Mellitus - pathology ; Diabetic Angiopathies - etiology ; Diabetic Angiopathies - prevention & control ; Dietary Supplements ; Double-Blind Method ; Double-blind studies ; Female ; Fluorides ; Fluorine isotopes ; Fluorine Radioisotopes ; Follow-Up Studies ; Heart diseases ; Humans ; Lesions ; Male ; Medical imaging ; Placebos ; Positron emission ; Positron emission tomography ; Sodium Fluoride ; Tomography ; Treatment Outcome ; Vascular Calcification - etiology ; Vascular Calcification - prevention & control ; vitamin K ; Vitamin K 1 - administration & dosage ; Vitamins ; Western Australia</subject><ispartof>The American journal of clinical nutrition, 2022-01, Vol.115 (1), p.45-52</ispartof><rights>2022 American Society for Nutrition.</rights><rights>The Author(s) 2021. Published by Oxford University Press on behalf of the American Society for Nutrition.</rights><rights>Copyright American Society for Clinical Nutrition, Inc. Jan 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c334t-2a90afa7af47d0dba5c97754b480f60705e4088c639d1898e1fce53e52fab9fb3</citedby><cites>FETCH-LOGICAL-c334t-2a90afa7af47d0dba5c97754b480f60705e4088c639d1898e1fce53e52fab9fb3</cites><orcidid>0000-0001-5166-0605 ; 0000-0001-8257-7361</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0002916522001095$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3549,27924,27925,45780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34637494$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bellinge, Jamie W</creatorcontrib><creatorcontrib>Francis, Roslyn J</creatorcontrib><creatorcontrib>Lee, Sing C</creatorcontrib><creatorcontrib>Bondonno, Nicola P</creatorcontrib><creatorcontrib>Sim, Marc</creatorcontrib><creatorcontrib>Lewis, Joshua R</creatorcontrib><creatorcontrib>Watts, Gerald F</creatorcontrib><creatorcontrib>Schultz, Carl J</creatorcontrib><title>The effect of vitamin K1 on arterial calcification activity in subjects with diabetes mellitus: a post hoc analysis of a double-blind, randomized, placebo-controlled trial</title><title>The American journal of clinical nutrition</title><addtitle>Am J Clin Nutr</addtitle><description>Coronary and aortic artery calcifications are generally slow to develop, and their burden predicts cardiovascular disease events. In patients with diabetes mellitus, arterial calcification is accelerated and calcification activity can be detected using 18F-sodium fluoride positron emission tomography (18F-NaF PET).
We aimed to determine whether vitamin K1 supplementation inhibits arterial calcification activity in individuals with diabetes mellitus.
This was a post hoc analysis of the ViKCoVaC (effect of Vitamin-K1 and Colchicine on Vascular Calcification activity in subjects with Diabetes Mellitus) double-blind randomized controlled trial conducted in Perth, Western Australia. Individuals with diabetes mellitus and established coronary calcification (coronary calcium score > 10), but without clinical coronary artery disease, underwent baseline 18F-NaF PET imaging, followed by oral vitamin K1 supplementation (10 mg/d) or placebo for 3 mo, after which 18F-NaF PET imaging was repeated. We tested whether individuals randomly assigned to vitamin K1 supplementation had reduced development of new 18F-NaF PET positive lesions within the coronary arteries and aorta.
In total, 149 individuals completed baseline and follow-up imaging studies. Vitamin K1 supplementation independently decreased the odds of developing new 18F-NaF PET positive lesions in the coronary arteries (OR: 0.35; 95% CI: 0.16, 0.78; P = 0.010), aorta (OR: 0.27; 95% CI: 0.08, 0.94; P = 0.040), and in both aortic and coronary arteries (OR: 0.28; 95% CI: 0.13, 0.63; P = 0.002).
In individuals with diabetes mellitus, supplementation with 10 mg vitamin K1/d may prevent the development of newly calcifying lesions within the aorta and the coronary arteries as detected using 18F-NaF PET. Further long-term studies are needed to test this hypothesis.
This trial was registered at anzctr.org.au as ACTRN12616000024448.
▪</description><subject>Aged</subject><subject>Aorta</subject><subject>Aorta - diagnostic imaging</subject><subject>aortic diseases</subject><subject>arterial calcification</subject><subject>Arteries</subject><subject>Arteriosclerosis</subject><subject>Calcification</subject><subject>Calcification (ectopic)</subject><subject>Cardiovascular disease</subject><subject>Cardiovascular diseases</subject><subject>Clinical trials</subject><subject>Colchicine</subject><subject>Coronary artery</subject><subject>Coronary artery disease</subject><subject>Coronary vessels</subject><subject>Coronary Vessels - diagnostic imaging</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes Mellitus - pathology</subject><subject>Diabetic Angiopathies - etiology</subject><subject>Diabetic Angiopathies - prevention & control</subject><subject>Dietary Supplements</subject><subject>Double-Blind Method</subject><subject>Double-blind studies</subject><subject>Female</subject><subject>Fluorides</subject><subject>Fluorine isotopes</subject><subject>Fluorine Radioisotopes</subject><subject>Follow-Up Studies</subject><subject>Heart diseases</subject><subject>Humans</subject><subject>Lesions</subject><subject>Male</subject><subject>Medical imaging</subject><subject>Placebos</subject><subject>Positron emission</subject><subject>Positron emission tomography</subject><subject>Sodium Fluoride</subject><subject>Tomography</subject><subject>Treatment Outcome</subject><subject>Vascular Calcification - etiology</subject><subject>Vascular Calcification - prevention & control</subject><subject>vitamin K</subject><subject>Vitamin K 1 - administration & dosage</subject><subject>Vitamins</subject><subject>Western Australia</subject><issn>0002-9165</issn><issn>1938-3207</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpt0U2PFCEQBmBiNO64evNsSLx42HahafrDm9n4FTfxsp47BRQZJjTMAr1m_Ev-SZnM6MF4gpCHooqXkJecveVsEtew0-E63IMSrH9ENnwSYyNaNjwmG8ZY20y8lxfkWc47xnjbjf1TciG6Xgzd1G3Ir7stUrQWdaHR0gdXYHGBfuU0BgqpYHLgqQavnXUaijse6-IqPNAK86p29W6mP1zZUuNAYcFMF_TelTW_o0D3MRe6jZpCAH_ILh8fAmriqjw2yrtgrmiCYOLifmLd7z1oVLHRMZQUvUdDy7GN5-SJBZ_xxXm9JN8_fri7-dzcfvv05eb9baOF6ErTwsTAwgC2GwwzCqSehkF2qhuZ7dnAJHZsHHUvJsPHaURuNUqBsrWgJqvEJXlzqrtP8X7FXObFZV0ngoBxzXMrRz62cpKs0tf_0F1cU52zqr7lcuhH2VV1dVI6xZwT2nmf3ALpMHM2H0OcjyHO5xArf3UuuqoFzV_8J7UK-hPA-gsPDtOctcOg0bhUw5hNdP-v_Bt9UK93</recordid><startdate>20220101</startdate><enddate>20220101</enddate><creator>Bellinge, Jamie W</creator><creator>Francis, Roslyn J</creator><creator>Lee, Sing C</creator><creator>Bondonno, Nicola P</creator><creator>Sim, Marc</creator><creator>Lewis, Joshua R</creator><creator>Watts, Gerald F</creator><creator>Schultz, Carl J</creator><general>Elsevier Inc</general><general>American Society for Clinical Nutrition, Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7T7</scope><scope>7TS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5166-0605</orcidid><orcidid>https://orcid.org/0000-0001-8257-7361</orcidid></search><sort><creationdate>20220101</creationdate><title>The effect of vitamin K1 on arterial calcification activity in subjects with diabetes mellitus: a post hoc analysis of a double-blind, randomized, placebo-controlled trial</title><author>Bellinge, Jamie W ; Francis, Roslyn J ; Lee, Sing C ; Bondonno, Nicola P ; Sim, Marc ; Lewis, Joshua R ; Watts, Gerald F ; Schultz, Carl J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c334t-2a90afa7af47d0dba5c97754b480f60705e4088c639d1898e1fce53e52fab9fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Aged</topic><topic>Aorta</topic><topic>Aorta - diagnostic imaging</topic><topic>aortic diseases</topic><topic>arterial calcification</topic><topic>Arteries</topic><topic>Arteriosclerosis</topic><topic>Calcification</topic><topic>Calcification (ectopic)</topic><topic>Cardiovascular disease</topic><topic>Cardiovascular diseases</topic><topic>Clinical trials</topic><topic>Colchicine</topic><topic>Coronary artery</topic><topic>Coronary artery disease</topic><topic>Coronary vessels</topic><topic>Coronary Vessels - diagnostic imaging</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetes Mellitus - pathology</topic><topic>Diabetic Angiopathies - etiology</topic><topic>Diabetic Angiopathies - prevention & control</topic><topic>Dietary Supplements</topic><topic>Double-Blind Method</topic><topic>Double-blind studies</topic><topic>Female</topic><topic>Fluorides</topic><topic>Fluorine isotopes</topic><topic>Fluorine Radioisotopes</topic><topic>Follow-Up Studies</topic><topic>Heart diseases</topic><topic>Humans</topic><topic>Lesions</topic><topic>Male</topic><topic>Medical imaging</topic><topic>Placebos</topic><topic>Positron emission</topic><topic>Positron emission tomography</topic><topic>Sodium Fluoride</topic><topic>Tomography</topic><topic>Treatment Outcome</topic><topic>Vascular Calcification - etiology</topic><topic>Vascular Calcification - prevention & control</topic><topic>vitamin K</topic><topic>Vitamin K 1 - administration & dosage</topic><topic>Vitamins</topic><topic>Western Australia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bellinge, Jamie W</creatorcontrib><creatorcontrib>Francis, Roslyn J</creatorcontrib><creatorcontrib>Lee, Sing C</creatorcontrib><creatorcontrib>Bondonno, Nicola P</creatorcontrib><creatorcontrib>Sim, Marc</creatorcontrib><creatorcontrib>Lewis, Joshua R</creatorcontrib><creatorcontrib>Watts, Gerald F</creatorcontrib><creatorcontrib>Schultz, Carl J</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Physical Education Index</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The American journal of clinical nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bellinge, Jamie W</au><au>Francis, Roslyn J</au><au>Lee, Sing C</au><au>Bondonno, Nicola P</au><au>Sim, Marc</au><au>Lewis, Joshua R</au><au>Watts, Gerald F</au><au>Schultz, Carl J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of vitamin K1 on arterial calcification activity in subjects with diabetes mellitus: a post hoc analysis of a double-blind, randomized, placebo-controlled trial</atitle><jtitle>The American journal of clinical nutrition</jtitle><addtitle>Am J Clin Nutr</addtitle><date>2022-01-01</date><risdate>2022</risdate><volume>115</volume><issue>1</issue><spage>45</spage><epage>52</epage><pages>45-52</pages><issn>0002-9165</issn><eissn>1938-3207</eissn><abstract>Coronary and aortic artery calcifications are generally slow to develop, and their burden predicts cardiovascular disease events. In patients with diabetes mellitus, arterial calcification is accelerated and calcification activity can be detected using 18F-sodium fluoride positron emission tomography (18F-NaF PET).
We aimed to determine whether vitamin K1 supplementation inhibits arterial calcification activity in individuals with diabetes mellitus.
This was a post hoc analysis of the ViKCoVaC (effect of Vitamin-K1 and Colchicine on Vascular Calcification activity in subjects with Diabetes Mellitus) double-blind randomized controlled trial conducted in Perth, Western Australia. Individuals with diabetes mellitus and established coronary calcification (coronary calcium score > 10), but without clinical coronary artery disease, underwent baseline 18F-NaF PET imaging, followed by oral vitamin K1 supplementation (10 mg/d) or placebo for 3 mo, after which 18F-NaF PET imaging was repeated. We tested whether individuals randomly assigned to vitamin K1 supplementation had reduced development of new 18F-NaF PET positive lesions within the coronary arteries and aorta.
In total, 149 individuals completed baseline and follow-up imaging studies. Vitamin K1 supplementation independently decreased the odds of developing new 18F-NaF PET positive lesions in the coronary arteries (OR: 0.35; 95% CI: 0.16, 0.78; P = 0.010), aorta (OR: 0.27; 95% CI: 0.08, 0.94; P = 0.040), and in both aortic and coronary arteries (OR: 0.28; 95% CI: 0.13, 0.63; P = 0.002).
In individuals with diabetes mellitus, supplementation with 10 mg vitamin K1/d may prevent the development of newly calcifying lesions within the aorta and the coronary arteries as detected using 18F-NaF PET. Further long-term studies are needed to test this hypothesis.
This trial was registered at anzctr.org.au as ACTRN12616000024448.
▪</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>34637494</pmid><doi>10.1093/ajcn/nqab306</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-5166-0605</orcidid><orcidid>https://orcid.org/0000-0001-8257-7361</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aged Aorta Aorta - diagnostic imaging aortic diseases arterial calcification Arteries Arteriosclerosis Calcification Calcification (ectopic) Cardiovascular disease Cardiovascular diseases Clinical trials Colchicine Coronary artery Coronary artery disease Coronary vessels Coronary Vessels - diagnostic imaging Diabetes Diabetes mellitus Diabetes Mellitus - pathology Diabetic Angiopathies - etiology Diabetic Angiopathies - prevention & control Dietary Supplements Double-Blind Method Double-blind studies Female Fluorides Fluorine isotopes Fluorine Radioisotopes Follow-Up Studies Heart diseases Humans Lesions Male Medical imaging Placebos Positron emission Positron emission tomography Sodium Fluoride Tomography Treatment Outcome Vascular Calcification - etiology Vascular Calcification - prevention & control vitamin K Vitamin K 1 - administration & dosage Vitamins Western Australia |
title | The effect of vitamin K1 on arterial calcification activity in subjects with diabetes mellitus: a post hoc analysis of a double-blind, randomized, placebo-controlled trial |
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