TY - JOUR
T1 - Aflatoxin B 1 exposure and liver cirrhosis in Guatemala
T2 - A case-control study
AU - Alvarez, Christian S.
AU - Hernández, Elisa
AU - Escobar, Kira
AU - Villagrán, Carmen I.
AU - Kroker-Lobos, María F.
AU - Rivera-Andrade, Alvaro
AU - Smith, Joshua W.
AU - Egner, Patricia A.
AU - Lazo, Mariana
AU - Freedman, Neal D.
AU - Guallar, Eliseo
AU - Dean, Michael
AU - Graubard, Barry I.
AU - Groopman, John D.
AU - Ramírez-Zea, Manuel
AU - McGlynn, Katherine A.
N1 - Publisher Copyright:
© Re-use permitted under CC BY. Published by BMJ.
PY - 2020/7/7
Y1 - 2020/7/7
N2 - Objective In Guatemala, cirrhosis is among the 10 leading causes of death, and mortality rates have increased lately. The reasons for this heavy burden of disease are not clear as the prevalence of prominent risk factors, such as hepatitis B virus, hepatitis C virus and heavy alcohol consumption, appears to be low. Aflatoxin B 1 (AFB 1) exposure, however, appears to be high, and thus could be associated with the high burden of cirrhosis. Whether AFB 1 increases the risk of cirrhosis in the absence of viral infection, however, is not clear. Design Cirrhosis cases (n=100) from two major referral hospitals in Guatemala City were compared with controls (n=200) from a cross-sectional study. Logistic regression was used to estimate the ORs and 95% CIs of cirrhosis and quintiles of AFB 1 in crude and adjusted models. A sex-stratified analysis was also conducted. Results The median AFB 1 level was significantly higher among the cases (11.4 pg/mg) than controls (5.11 pg/mg). In logistic regression analyses, higher levels of AFB 1 was associated with cirrhosis (quintile 5 vs quintile 1, OR: 11.55; 95% CI 4.05 to 32.89). No attenuation was observed with adjustment by sex, ethnicity, hepatitis B virus status, and heavy alcohol consumption. A significantly increasing trend in association was observed in both models (p trend <0.01). Additionally, the cirrhosis-AFB 1 association was more prominent among men. Conclusions The current study found a significant positive association between AFB 1 exposure and cirrhosis. Mitigation of AFB 1 exposure and a better understanding of additional risk factors may be important to reduce the burden of cirrhosis in Guatemala.
AB - Objective In Guatemala, cirrhosis is among the 10 leading causes of death, and mortality rates have increased lately. The reasons for this heavy burden of disease are not clear as the prevalence of prominent risk factors, such as hepatitis B virus, hepatitis C virus and heavy alcohol consumption, appears to be low. Aflatoxin B 1 (AFB 1) exposure, however, appears to be high, and thus could be associated with the high burden of cirrhosis. Whether AFB 1 increases the risk of cirrhosis in the absence of viral infection, however, is not clear. Design Cirrhosis cases (n=100) from two major referral hospitals in Guatemala City were compared with controls (n=200) from a cross-sectional study. Logistic regression was used to estimate the ORs and 95% CIs of cirrhosis and quintiles of AFB 1 in crude and adjusted models. A sex-stratified analysis was also conducted. Results The median AFB 1 level was significantly higher among the cases (11.4 pg/mg) than controls (5.11 pg/mg). In logistic regression analyses, higher levels of AFB 1 was associated with cirrhosis (quintile 5 vs quintile 1, OR: 11.55; 95% CI 4.05 to 32.89). No attenuation was observed with adjustment by sex, ethnicity, hepatitis B virus status, and heavy alcohol consumption. A significantly increasing trend in association was observed in both models (p trend <0.01). Additionally, the cirrhosis-AFB 1 association was more prominent among men. Conclusions The current study found a significant positive association between AFB 1 exposure and cirrhosis. Mitigation of AFB 1 exposure and a better understanding of additional risk factors may be important to reduce the burden of cirrhosis in Guatemala.
KW - chronic liver disease
KW - epidemiology
KW - liver cirrhosis
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U2 - 10.1136/bmjgast-2020-000380
DO - 10.1136/bmjgast-2020-000380
M3 - Article
AN - SCOPUS:85088091558
SN - 2054-4774
VL - 7
JO - BMJ Open Gastroenterology
JF - BMJ Open Gastroenterology
IS - 1
M1 - 000380
ER -