Alcohol, metabolic risk and elevated serum gamma-glutamyl transferase (GGT) in Indigenous Australians

被引:10
作者
Haren, Matthew T. [1 ,3 ]
Li, Ming [3 ]
Petkov, John [2 ,4 ]
McDermott, Robyn A. [3 ]
机构
[1] Univ S Australia, SGRHS, Whyalla Norrie, SA, Australia
[2] Univ S Australia, CRHaCD, Whyalla Norrie, SA, Australia
[3] Univ S Australia, Div Hlth Sci, Sansom Inst, Adelaide, SA 5001, Australia
[4] Univ S Australia, Ctr Reg Engagement, Appl Stat Unit, Mt Gambier, SA, Australia
基金
英国医学研究理事会;
关键词
CORONARY-HEART-DISEASE; FATTY LIVER-DISEASE; PHYSICAL-ACTIVITY; FRAMINGHAM; CONSUMPTION; POPULATION; DRINKING; OBESITY; HEALTH; AMINOTRANSFERASE;
D O I
10.1186/1471-2458-10-454
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: The interaction between overweight/obesity and alcohol intake on liver enzyme concentrations have been demonstrated. No studies have yet examined the interaction between metabolic syndrome or multiple metabolic risk factors and alcohol intake on liver enzymes. The aim of this study was to examine if alcohol consumption modifies the effect of metabolic risk on elevated serum GGT in Indigenous Australians. Methods: Data were from N = 2609 Indigenous Australians who participated in a health screening program in rural far north Queensland in 1999-2000 (44.5% response rate). The individual and interactive effects of metabolic risk and alcohol drinking on elevated serum GGT concentrations (>= 50 U/L) were analyzed using logistic regression. Results: Overall, 26% of the population had GGT >= 50 U/L. Elevated GGT was associated with alcohol drinking (moderate drinking: OR 2.3 [95% CI 1.6 - 3.2]; risky drinking: OR 6.0 [4.4 - 8.2]), and with abdominal obesity (OR 3.7 [2.5 - 5.6]), adverse metabolic risk cluster profile (OR 3.4 [2.6 - 4.3]) and metabolic syndrome (OR 2.7 [2.1 - 3.5]) after adjustment for age, sex, ethnicity, smoking, physical activity and BMI. The associations of obesity and metabolic syndrome with elevated GGT were similar across alcohol drinking strata, but the association of an adverse metabolic risk cluster profile with elevated GGT was larger in risky drinkers (OR 4.9 [3.7 - 6.7]) than in moderate drinkers (OR 2.8 [1.6 - 4.9]) and abstainers (OR 1.6 [0.9 - 2.8]). Conclusions: In this Indigenous population, an adverse metabolic profile conferred three times the risk of elevated GGT in risky drinkers compared with abstainers, independent of sex and ethnicity. Community interventions need to target both determinants of the population's metabolic status and alcohol consumption to reduce the risk of elevated GGT.
引用
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页数:10
相关论文
共 43 条
[1]   Effect of moderate alcohol consumption on liver enzymes increases with increasing body mass index [J].
Alatalo, Paeivikki I. ;
Koivisto, Heidi M. ;
Hietala, Johanna P. ;
Puukka, Katri S. ;
Bloigu, Risto ;
Niemelae, Onni J. .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2008, 88 (04) :1097-1103
[2]   Biomarkers of Liver Status in Heavy Drinkers, Moderate Drinkers and Abstainers [J].
Alatalo, Paivikki ;
Koivisto, Heidi ;
Puukka, Katri ;
Hietala, Johanna ;
Anttila, Petra ;
Bloigu, Risto ;
Niemela, Onni .
ALCOHOL AND ALCOHOLISM, 2009, 44 (02) :199-203
[3]   The metabolic syndrome - a new worldwide definition [J].
Alberti, KGMM ;
Zimmet, P ;
Shaw, J .
LANCET, 2005, 366 (9491) :1059-1062
[4]  
Alberti KGMM, 1998, DIABETIC MED, V15, P539, DOI 10.1002/(SICI)1096-9136(199807)15:7<539::AID-DIA668>3.0.CO
[5]  
2-S
[6]  
[Anonymous], 2005, HLTH WELFARE AUSTRAL
[7]  
[Anonymous], 2020, WHO Technical Report Series 1004, Annex 9, 2017: World Health Organization
[8]  
*AUSTR BUR STAT, 2001, 2001 CENS DICT
[9]   Application of Framingham risk estimates to ethnic minorities in United Kingdom and implications for primary prevention of heart disease in general practice: cross sectional population based study [J].
Cappuccio, FP ;
Oakeshott, P ;
Strazzullo, P ;
Kerry, SM .
BRITISH MEDICAL JOURNAL, 2002, 325 (7375) :1271-1274B
[10]   Validation of the Framingham Coronary Heart Disease prediction scores - Results of a multiple ethnic groups investigation [J].
D'Agostino, RB ;
Grundy, S ;
Sullivan, LM ;
Wilson, P .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (02) :180-187