Dietary choline and folate relationships with serum hepatic inflammatory injury markers in Taiwanese adults

Background and Objectives: The relationships of dietary choline and folate intake with hepatic function have yet to be established in the Taiwanese population. We investigated the associations of choline and folate intake with hepatic inflammatory injury in Taiwanese adults. Methods and Study Design...

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Veröffentlicht in:Asia Pacific Journal of Clinical Nutrition 2017-01, Vol.26 (4), p.642-649
Hauptverfasser: Cheng, Chin-Pao, Chen, Chien-Hung, Kuo, Chang-Sheng, Kuo, Hsing-Tao, Huang, Kuang-Ta, Shen, Yu-Li, Chang, Chin-Hao, Huang, Rwei Fen S
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container_end_page 649
container_issue 4
container_start_page 642
container_title Asia Pacific Journal of Clinical Nutrition
container_volume 26
creator Cheng, Chin-Pao
Chen, Chien-Hung
Kuo, Chang-Sheng
Kuo, Hsing-Tao
Huang, Kuang-Ta
Shen, Yu-Li
Chang, Chin-Hao
Huang, Rwei Fen S
description Background and Objectives: The relationships of dietary choline and folate intake with hepatic function have yet to be established in the Taiwanese population. We investigated the associations of choline and folate intake with hepatic inflammatory injury in Taiwanese adults. Methods and Study Design: Blood samples and data on dietary choline components and folate intake from 548 Taiwanese adults without pathological liver disease were collected. Dietary intake was derived using a semiquantitative food-frequency questionnaire. Serum liver injury markers of alanine transaminase, aspartate transaminase, and hepatitis viral infection were measured. Results: Elevated serum hepatic injury markers (>40 U/L) were associated with low folate and free choline intake (p<0.05). Folate intake was the most significant dietary determinant of serum aspartate transaminase concentration (beta=−0.05, p=0.04), followed by free choline intake (beta=−0.249, p=0.055). Folate intake exceeding the median level (268 μg/d) was correlated with a reduced rate of hepatitis viral infection (p=0.032) and with normalized serum aspartate transaminase (odds ratio [OR]=0.998, 95% confidence interval [CI]=0.996-1, p=0.042) and alanine transaminase (OR=0.998, 95% CI=0.007-1, p=0.019). Total choline intake exceeding the median level (233 mg/d) was associated with normalized serum aspartate transaminase (OR=0.518, 95% CI=0.360-0.745, p=0.018). Conclusions: The newly established relationships of dietary intake of total choline and folate with normalized hepatic inflammatory markers can guide the development of dietary choline and folate intake recommendations for Taiwanese adults.
doi_str_mv 10.6133/apjcn.082016.03
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We investigated the associations of choline and folate intake with hepatic inflammatory injury in Taiwanese adults. Methods and Study Design: Blood samples and data on dietary choline components and folate intake from 548 Taiwanese adults without pathological liver disease were collected. Dietary intake was derived using a semiquantitative food-frequency questionnaire. Serum liver injury markers of alanine transaminase, aspartate transaminase, and hepatitis viral infection were measured. Results: Elevated serum hepatic injury markers (>40 U/L) were associated with low folate and free choline intake (p<0.05). Folate intake was the most significant dietary determinant of serum aspartate transaminase concentration (beta=−0.05, p=0.04), followed by free choline intake (beta=−0.249, p=0.055). Folate intake exceeding the median level (268 μg/d) was correlated with a reduced rate of hepatitis viral infection (p=0.032) and with normalized serum aspartate transaminase (odds ratio [OR]=0.998, 95% confidence interval [CI]=0.996-1, p=0.042) and alanine transaminase (OR=0.998, 95% CI=0.007-1, p=0.019). Total choline intake exceeding the median level (233 mg/d) was associated with normalized serum aspartate transaminase (OR=0.518, 95% CI=0.360-0.745, p=0.018). Conclusions: The newly established relationships of dietary intake of total choline and folate with normalized hepatic inflammatory markers can guide the development of dietary choline and folate intake recommendations for Taiwanese adults.</description><identifier>ISSN: 0964-7058</identifier><identifier>EISSN: 1440-6047</identifier><identifier>DOI: 10.6133/apjcn.082016.03</identifier><identifier>PMID: 28582814</identifier><language>eng</language><publisher>Clayton, Vic: HEC Press</publisher><subject>Aged ; Aging ; Alcohol use ; Asian Continental Ancestry Group ; Biomarkers - blood ; Choline ; Choline - administration &amp; dosage ; Diet ; DNA methylation ; Female ; Folic acid ; Folic Acid - administration &amp; dosage ; Hepatitis ; Humans ; Laboratories ; Liver cancer ; Liver cirrhosis ; Liver Diseases - blood ; Male ; Middle Aged ; Nutritional Status ; Prevention ; Rodents ; Sex Factors ; Taiwan ; Treatment ; Viral infections ; Wounds and injuries</subject><ispartof>Asia Pacific Journal of Clinical Nutrition, 2017-01, Vol.26 (4), p.642-649</ispartof><rights>Copyright HEC Press Jun 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a559t-35158d256020e1cf5166d839bbeeb9b3700a93c838a7bfd687eb79111d5633103</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28582814$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cheng, Chin-Pao</creatorcontrib><creatorcontrib>Chen, Chien-Hung</creatorcontrib><creatorcontrib>Kuo, Chang-Sheng</creatorcontrib><creatorcontrib>Kuo, Hsing-Tao</creatorcontrib><creatorcontrib>Huang, Kuang-Ta</creatorcontrib><creatorcontrib>Shen, Yu-Li</creatorcontrib><creatorcontrib>Chang, Chin-Hao</creatorcontrib><creatorcontrib>Huang, Rwei Fen S</creatorcontrib><title>Dietary choline and folate relationships with serum hepatic inflammatory injury markers in Taiwanese adults</title><title>Asia Pacific Journal of Clinical Nutrition</title><addtitle>Asia Pac J Clin Nutr</addtitle><description>Background and Objectives: The relationships of dietary choline and folate intake with hepatic function have yet to be established in the Taiwanese population. We investigated the associations of choline and folate intake with hepatic inflammatory injury in Taiwanese adults. Methods and Study Design: Blood samples and data on dietary choline components and folate intake from 548 Taiwanese adults without pathological liver disease were collected. Dietary intake was derived using a semiquantitative food-frequency questionnaire. Serum liver injury markers of alanine transaminase, aspartate transaminase, and hepatitis viral infection were measured. Results: Elevated serum hepatic injury markers (>40 U/L) were associated with low folate and free choline intake (p<0.05). Folate intake was the most significant dietary determinant of serum aspartate transaminase concentration (beta=−0.05, p=0.04), followed by free choline intake (beta=−0.249, p=0.055). Folate intake exceeding the median level (268 μg/d) was correlated with a reduced rate of hepatitis viral infection (p=0.032) and with normalized serum aspartate transaminase (odds ratio [OR]=0.998, 95% confidence interval [CI]=0.996-1, p=0.042) and alanine transaminase (OR=0.998, 95% CI=0.007-1, p=0.019). Total choline intake exceeding the median level (233 mg/d) was associated with normalized serum aspartate transaminase (OR=0.518, 95% CI=0.360-0.745, p=0.018). 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We investigated the associations of choline and folate intake with hepatic inflammatory injury in Taiwanese adults. Methods and Study Design: Blood samples and data on dietary choline components and folate intake from 548 Taiwanese adults without pathological liver disease were collected. Dietary intake was derived using a semiquantitative food-frequency questionnaire. Serum liver injury markers of alanine transaminase, aspartate transaminase, and hepatitis viral infection were measured. Results: Elevated serum hepatic injury markers (>40 U/L) were associated with low folate and free choline intake (p<0.05). Folate intake was the most significant dietary determinant of serum aspartate transaminase concentration (beta=−0.05, p=0.04), followed by free choline intake (beta=−0.249, p=0.055). Folate intake exceeding the median level (268 μg/d) was correlated with a reduced rate of hepatitis viral infection (p=0.032) and with normalized serum aspartate transaminase (odds ratio [OR]=0.998, 95% confidence interval [CI]=0.996-1, p=0.042) and alanine transaminase (OR=0.998, 95% CI=0.007-1, p=0.019). Total choline intake exceeding the median level (233 mg/d) was associated with normalized serum aspartate transaminase (OR=0.518, 95% CI=0.360-0.745, p=0.018). Conclusions: The newly established relationships of dietary intake of total choline and folate with normalized hepatic inflammatory markers can guide the development of dietary choline and folate intake recommendations for Taiwanese adults.</abstract><cop>Clayton, Vic</cop><pub>HEC Press</pub><pmid>28582814</pmid><doi>10.6133/apjcn.082016.03</doi><tpages>8</tpages></addata></record>
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subjects Aged
Aging
Alcohol use
Asian Continental Ancestry Group
Biomarkers - blood
Choline
Choline - administration & dosage
Diet
DNA methylation
Female
Folic acid
Folic Acid - administration & dosage
Hepatitis
Humans
Laboratories
Liver cancer
Liver cirrhosis
Liver Diseases - blood
Male
Middle Aged
Nutritional Status
Prevention
Rodents
Sex Factors
Taiwan
Treatment
Viral infections
Wounds and injuries
title Dietary choline and folate relationships with serum hepatic inflammatory injury markers in Taiwanese adults
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