Combined Effect of Omega-3 Fatty Acid and Vitamin D 3 on Oxidized LDL-C and Non-HDL-C Levels in People With Vitamin D Deficiency : A Randomized Controlled Trial
Copyright © 2023 Wolters Kluwer Health, Inc. All rights reserved..
ABSTRACT: The present randomized clinical trial (RCT) was conducted on Jordanian participants with vitamin D deficiency (VDD) with no other medical conditions, to evaluate the combined effect of 1,25-dihydroxy vitamin D 3 (Vit.D 3 ) and omega-3 fatty acid (n-3FA) supplements (D+) on oxidized low-density lipoprotein (Ox-LDL) and non-high-density lipoprotein cholesterol (non-HDL-C) levels as common predictors of cardiovascular diseases (CVDs). Participants were randomized into 4 groups as follows: a control group (C) that received no supplementations, a Vit.D 3 group that received 50,000 IU of Vit.D 3 every week, an n-3FA group that received 300 mg of omega-3 fatty acid every day, and a D+ group that received a combination of both supplements, with the same dosage administered by the previous groups but with a 4-6-hour time interval between Vit.D 3 and n-3FA administration to avoid any possible interaction. All supplementations were administered orally for 8 weeks. Forty-seven participants were allocated to each group. Twenty-six in the control group, 37 participants in the Vit.D 3 group, 37 participants in the n-3FA group, and 46 participants in the D+ group completed the study to the end. The D+ supplementations significantly increased non-HDL-C (118.99 ± 60.98 to 155.26 ± 43.36 mg/dL, P << 0.05) but decreased Ox-LDL-C levels (69.29 ± 37.69 to 52.81 ± 17.30 pg/mL, P = 0.03). The stepwise regression showed that the serum LDL-C level was the main independent variable involved in the elevation of non-HDL levels (R 2 = 0.837) observed at the end of the trial in the D+ group. The groups that were supplemented with either Vit.D 3 alone or n-3FA alone had an insignificant decrease in the level of Ox-LDL-C. In conclusion, despite the observed hyperlipidemic effect, the combination treatment is recommended by the research team because the decrease in Ox-LDL may offset the hyperlipidemic effect.
Errataetall: |
CommentIn: J Cardiovasc Pharmacol. 2023 Apr 01;81(4):248-250. - PMID 36795506 |
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Medienart: |
E-Artikel |
Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:81 |
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Enthalten in: |
Journal of cardiovascular pharmacology - 81(2023), 4 vom: 01. Apr., Seite 251-258 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Mehdawi, Amani [VerfasserIn] |
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Links: |
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Themen: |
1C6V77QF41 |
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Anmerkungen: |
Date Completed 11.04.2023 Date Revised 14.09.2023 published: Electronic CommentIn: J Cardiovasc Pharmacol. 2023 Apr 01;81(4):248-250. - PMID 36795506 Citation Status MEDLINE |
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doi: |
10.1097/FJC.0000000000001398 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM351416722 |
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245 | 1 | 0 | |a Combined Effect of Omega-3 Fatty Acid and Vitamin D 3 on Oxidized LDL-C and Non-HDL-C Levels in People With Vitamin D Deficiency |b A Randomized Controlled Trial |
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500 | |a CommentIn: J Cardiovasc Pharmacol. 2023 Apr 01;81(4):248-250. - PMID 36795506 | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Copyright © 2023 Wolters Kluwer Health, Inc. All rights reserved. | ||
520 | |a ABSTRACT: The present randomized clinical trial (RCT) was conducted on Jordanian participants with vitamin D deficiency (VDD) with no other medical conditions, to evaluate the combined effect of 1,25-dihydroxy vitamin D 3 (Vit.D 3 ) and omega-3 fatty acid (n-3FA) supplements (D+) on oxidized low-density lipoprotein (Ox-LDL) and non-high-density lipoprotein cholesterol (non-HDL-C) levels as common predictors of cardiovascular diseases (CVDs). Participants were randomized into 4 groups as follows: a control group (C) that received no supplementations, a Vit.D 3 group that received 50,000 IU of Vit.D 3 every week, an n-3FA group that received 300 mg of omega-3 fatty acid every day, and a D+ group that received a combination of both supplements, with the same dosage administered by the previous groups but with a 4-6-hour time interval between Vit.D 3 and n-3FA administration to avoid any possible interaction. All supplementations were administered orally for 8 weeks. Forty-seven participants were allocated to each group. Twenty-six in the control group, 37 participants in the Vit.D 3 group, 37 participants in the n-3FA group, and 46 participants in the D+ group completed the study to the end. The D+ supplementations significantly increased non-HDL-C (118.99 ± 60.98 to 155.26 ± 43.36 mg/dL, P << 0.05) but decreased Ox-LDL-C levels (69.29 ± 37.69 to 52.81 ± 17.30 pg/mL, P = 0.03). The stepwise regression showed that the serum LDL-C level was the main independent variable involved in the elevation of non-HDL levels (R 2 = 0.837) observed at the end of the trial in the D+ group. The groups that were supplemented with either Vit.D 3 alone or n-3FA alone had an insignificant decrease in the level of Ox-LDL-C. In conclusion, despite the observed hyperlipidemic effect, the combination treatment is recommended by the research team because the decrease in Ox-LDL may offset the hyperlipidemic effect | ||
650 | 4 | |a Randomized Controlled Trial | |
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 7 | |a oxidized low density lipoprotein |2 NLM | |
650 | 7 | |a Fatty Acids, Omega-3 |2 NLM | |
650 | 7 | |a Cholecalciferol |2 NLM | |
650 | 7 | |a 1C6V77QF41 |2 NLM | |
650 | 7 | |a Lipoproteins, LDL |2 NLM | |
650 | 7 | |a Cholesterol |2 NLM | |
650 | 7 | |a 97C5T2UQ7J |2 NLM | |
700 | 1 | |a Mohammad, Beisan A |e verfasserin |4 aut | |
700 | 1 | |a Mosleh, Ibrahim |e verfasserin |4 aut | |
700 | 1 | |a Khader, Heba A |e verfasserin |4 aut | |
700 | 1 | |a Habash, Maha |e verfasserin |4 aut | |
700 | 1 | |a Nassar, Razan I |e verfasserin |4 aut | |
700 | 1 | |a Awwad, Shady |e verfasserin |4 aut | |
700 | 1 | |a Hasoun, Luai |e verfasserin |4 aut | |
700 | 1 | |a Abu-Samak, Mahmoud S |e verfasserin |4 aut | |
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