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      Directly measured free and total 25-hydroxyvitamin D levels in relation to metabolic health in multi-ethnic postmenopausal females in Saudi Arabia

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          Abstract

          Background

          Measurement of free 25-hydroyvitamin D (25(OH)D) status has been suggested as a more representative marker of vitamin D status than that of total 25(OH)D. Previously, free 25(OH)D could only be calculated indirectly; however, a newly developed direct assay for the measurement of free 25(OH)D is now available. The aim of this study therefore was to investigate directly measured total and free vitamin D levels association with metabolic health in postmenopausal healthy women living in Saudi Arabia.

          Methods

          A sample of 302 postmenopausal women aged ≥50 years ( n  = 302) living in Saudi Arabia were recruited in a cross-sectional study design. Blood samples were collected from subjects for measurement of serum levels of total 25(OH)D, directly measured free 25(OH)D, metabolic bone parameters, lipid profile, and other biochemical tests.

          Results

          A positive correlation was found between directly measured free and total 25(OH)D ( r = 0.64, P< 0.0001). Total but not free 25(OH)D showed significant association with serum intact parathyroid hormone ( P = 0.004), whilst free 25(OH)D but not total 25(OH)D showed a significant association with total cholesterol and LDL-C ( P = 0.032 and P = 0.045, respectively).

          Conclusions

          Free 25(OH)D and total 25(OH)D were found to be consistently correlated but with different associations to metabolic health parameters. Further research is needed to determine which marker of vitamin D status would be the most appropriate in population studies.

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          Most cited references63

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          Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge.

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            Evaluation, treatment, and prevention of vitamin D deficiency: an Endocrine Society clinical practice guideline.

            The objective was to provide guidelines to clinicians for the evaluation, treatment, and prevention of vitamin D deficiency with an emphasis on the care of patients who are at risk for deficiency. The Task Force was composed of a Chair, six additional experts, and a methodologist. The Task Force received no corporate funding or remuneration. Consensus was guided by systematic reviews of evidence and discussions during several conference calls and e-mail communications. The draft prepared by the Task Force was reviewed successively by The Endocrine Society's Clinical Guidelines Subcommittee, Clinical Affairs Core Committee, and cosponsoring associations, and it was posted on The Endocrine Society web site for member review. At each stage of review, the Task Force received written comments and incorporated needed changes. Considering that vitamin D deficiency is very common in all age groups and that few foods contain vitamin D, the Task Force recommended supplementation at suggested daily intake and tolerable upper limit levels, depending on age and clinical circumstances. The Task Force also suggested the measurement of serum 25-hydroxyvitamin D level by a reliable assay as the initial diagnostic test in patients at risk for deficiency. Treatment with either vitamin D(2) or vitamin D(3) was recommended for deficient patients. At the present time, there is not sufficient evidence to recommend screening individuals who are not at risk for deficiency or to prescribe vitamin D to attain the noncalcemic benefit for cardiovascular protection.
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              Vitamin D Deficiency

                Author and article information

                Journal
                Endocr Connect
                Endocr Connect
                EC
                Endocrine Connections
                Bioscientifica Ltd (Bristol )
                2049-3614
                15 November 2021
                01 December 2021
                : 10
                : 12
                : 1594-1606
                Affiliations
                [1 ]Department of Physiology , Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia
                [2 ]Department of Nutritional Sciences , Faculty of Health and Medical Sciences, University of Surrey, Guildford, UK
                [3 ]Centre of Excellence in Genomic Medicine Research , King Abdulaziz University, Jeddah, Saudi Arabia
                [4 ]Department of Medical Laboratory Technology , Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia
                [5 ]Centre for Innovation in Personalized Medicine , King Abdulaziz University, Jeddah, Saudi Arabia
                [6 ]Department of Clinical Biochemistry , Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia
                Author notes
                Correspondence should be addressed to S Alharazy: smalharazy@ 123456kau.edu.sa
                Author information
                http://orcid.org/0000-0001-8542-0810
                Article
                EC-21-0445
                10.1530/EC-21-0445
                8679882
                34783311
                8ddd3730-98ad-4b9c-957e-5eb553d6148e
                © The authors

                This work is licensed under a Creative Commons Attribution 4.0 International License.

                History
                : 04 November 2021
                : 15 November 2021
                Categories
                Research

                postmenopausal,vitamin d,free 25-hydroxyvitamin d,free vitamin d,saudi arabia

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