Alcohol intake and high density lipoprotein-cholesterol: comparison of food frequency questionnaire and diet record in a general population sample.

E. Müller, T. Stürmer, H. Brenner
{"title":"Alcohol intake and high density lipoprotein-cholesterol: comparison of food frequency questionnaire and diet record in a general population sample.","authors":"E. Müller, T. Stürmer, H. Brenner","doi":"10.1080/135952201317080409","DOIUrl":null,"url":null,"abstract":"BACKGROUND\nModerate alcohol consumption is known to affect several cardiovascular risk factors, including high density lipoprotein-cholesterol (HDL-C). Accurate measurement of alcohol intake in epidemiological studies is crucial for valid estimation of alcohol-related effects.\n\n\nMETHODS\nWe compared two widely used alcohol-intake assessment methods, a food frequency questionnaire (FFQ) and a 7-day diet record (DR) regarding the association between alcohol intake and HDL-C in the general population.\n\n\nRESULTS\nIn a representative sample (842 men, 1103 women) of the population of former West Germany (VERA study), 75.6% of the participants reported drinking alcoholic beverages in the FFQ, whereas the percentage was 84.9% according to the DR. The median daily alcohol intake of consumers was 10.3 and 12.1 g, as assessed by the FFQ and the DR, respectively. There was moderate agreement between reported consumption levels ranked by quintiles according to FFQ and DR (kappa = 0.49). With both approaches alcohol intake showed a strong positive association with HDL-C in linear regression models. The estimated increases in HDL-C (mg dL(-1)) per gram alcohol per day from the FFQ and DR were 0.15 [95% confidence interval (CI): 0.12-0.18] and 0.14 (95% CI: 0.11-0.17), respectively. When participants with different classification of the amount of alcohol consumed by FFQ and DR were excluded from the analysis, the association between alcohol intake and HDL-C was more pronounced.\n\n\nDISCUSSION\nOur analyses suggest that both FFQ and DR lead to similar results regarding the alcohol-HDL-C association in the general population, despite major differences in the recorded prevalence of drinking and amount of alcohol consumed. Both methods may tend to under-estimate the true alcohol-HDL-C association.","PeriodicalId":80024,"journal":{"name":"Journal of epidemiology and biostatistics","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2001-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of epidemiology and biostatistics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/135952201317080409","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

Abstract

BACKGROUND Moderate alcohol consumption is known to affect several cardiovascular risk factors, including high density lipoprotein-cholesterol (HDL-C). Accurate measurement of alcohol intake in epidemiological studies is crucial for valid estimation of alcohol-related effects. METHODS We compared two widely used alcohol-intake assessment methods, a food frequency questionnaire (FFQ) and a 7-day diet record (DR) regarding the association between alcohol intake and HDL-C in the general population. RESULTS In a representative sample (842 men, 1103 women) of the population of former West Germany (VERA study), 75.6% of the participants reported drinking alcoholic beverages in the FFQ, whereas the percentage was 84.9% according to the DR. The median daily alcohol intake of consumers was 10.3 and 12.1 g, as assessed by the FFQ and the DR, respectively. There was moderate agreement between reported consumption levels ranked by quintiles according to FFQ and DR (kappa = 0.49). With both approaches alcohol intake showed a strong positive association with HDL-C in linear regression models. The estimated increases in HDL-C (mg dL(-1)) per gram alcohol per day from the FFQ and DR were 0.15 [95% confidence interval (CI): 0.12-0.18] and 0.14 (95% CI: 0.11-0.17), respectively. When participants with different classification of the amount of alcohol consumed by FFQ and DR were excluded from the analysis, the association between alcohol intake and HDL-C was more pronounced. DISCUSSION Our analyses suggest that both FFQ and DR lead to similar results regarding the alcohol-HDL-C association in the general population, despite major differences in the recorded prevalence of drinking and amount of alcohol consumed. Both methods may tend to under-estimate the true alcohol-HDL-C association.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
酒精摄入与高密度脂蛋白-胆固醇:普通人群食物频率问卷与饮食记录的比较
背景:已知适度饮酒会影响几种心血管危险因素,包括高密度脂蛋白-胆固醇(HDL-C)。流行病学研究中准确测量酒精摄入量对于有效估计酒精相关影响至关重要。方法比较两种广泛使用的酒精摄入评估方法,即食物频率问卷(FFQ)和7天饮食记录(DR),以了解普通人群中酒精摄入与HDL-C之间的关系。结果在前西德人口的代表性样本(842名男性,1103名女性)(VERA研究)中,75.6%的参与者报告在FFQ中饮用酒精饮料,而根据DR,这一比例为84.9%。根据FFQ和DR评估,消费者的平均每日酒精摄入量分别为10.3 g和12.1 g。根据FFQ和DR按五分位数排列的报告消费水平之间存在适度的一致性(kappa = 0.49)。在线性回归模型中,两种方法均显示酒精摄入量与HDL-C呈正相关。据估计,FFQ和DR每天每克酒精增加的HDL-C (mg dL(-1))分别为0.15[95%可信区间(CI): 0.12-0.18]和0.14 (95% CI: 0.11-0.17)。当FFQ和DR饮酒量分类不同的参与者被排除在分析之外时,酒精摄入量与HDL-C之间的关联更加明显。讨论:我们的分析表明,尽管记录的饮酒流行程度和饮酒量存在重大差异,但在普通人群中,FFQ和DR在酒精- hdl - c相关性方面得出的结果相似。这两种方法都可能倾向于低估酒精与hdl - c之间的真正联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Statistical Inference Population, Exposure, and Outcome Measures of Disease Frequency Practice Problem Workbook Solutions Case Reports and Case Series
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1