Genetic Variations in Thiamin Transferase SLC35F3 and the Risk of Hypertension in Koreans
Hypertension is a major health issues globally. Multiple genetic and environmental factors are involved in hypertension etiology. Solute carrier family 35 member F3 (SLC35F3) is a type of transporter uptakes thiamin across the cellular and mitochondrial membrane. Recent studies suggested that variat...
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Published in | Clinical nutrition research Vol. 10; no. 2; pp. 140 - 149 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Korea (South)
Korean Society of Clinical Nutrition
01.04.2021
한국임상영양학회 |
Subjects | |
Online Access | Get full text |
ISSN | 2287-3732 2287-3740 |
DOI | 10.7762/cnr.2021.10.2.140 |
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Summary: | Hypertension is a major health issues globally. Multiple genetic and environmental factors are involved in hypertension etiology. Solute carrier family 35 member F3 (SLC35F3) is a type of transporter uptakes thiamin across the cellular and mitochondrial membrane. Recent studies suggested that variations in
are associated with the risk of hypertension; however, studies are limited in Koreans. This study examined the association of the genetic variations in
and the risk of hypertension in Koreans using the Korean Genome Epidemiology Study (Ansan/Ansung study). A total of 8,298 Koreans (males 3,983, females 4,315) were analyzed for their general characteristics, dietary intake, and blood pressure. Twenty-four tagging variations in
were selected and investigated for their association with the risk of hypertension using a sex-stratified approach. Findings suggested that, in males, rs12135117 A allele carriers were at the lower risk for hypertension (adjusted odds ratio, 0.859; 95% confidence interval [CI], 0.740-0.998). In females, rs10910387 TC genotype tended to increase the risk 1.172-fold for hypertension (95% CI, 1.002-1.370). Multiple linear regression models exhibited that rs12135117 A allele was negatively associated with blood pressure in males, and rs10910387 TC genotype had a positive association with blood pressure in females. However, statistical significance for these genetically modified effects was in lacked (Bonferroni's corrected p > 0.002). In conclusion, genetic variation in
is not a decisive prediction marker for hypertension risk in Koreans. Given the rarity of data, more studies are required to evaluate the role of
and thiamin in the hypertension etiology. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2287-3732 2287-3740 |
DOI: | 10.7762/cnr.2021.10.2.140 |