Affiliations 

  • 1 Department of Nutrition and Dietetics, Faculty of Medical and Health Sciences, Universiti Putra Malaysia, 43400 Serdang, Selangor, Malaysia. sitihusna11@gmail.com
  • 2 Department of Nutrition and Dietetics, Faculty of Medical and Health Sciences, Universiti Putra Malaysia, 43400 Serdang, Selangor, Malaysia. rositaj@upm.edu.my
  • 3 Department of Nutrition and Dietetics, Faculty of Medical and Health Sciences, Universiti Putra Malaysia, 43400 Serdang, Selangor, Malaysia. mohdredzwan@upm.edu.my
Nutrients, 2018 Apr 07;10(4).
PMID: 29642443 DOI: 10.3390/nu10040460

Abstract

Aflatoxin is a food contaminant and its exposure through the diet is frequent and ubiquitous. A long-term dietary aflatoxin exposure has been linked to the development of liver cancer in populations with high prevalence of aflatoxin contamination in foods. Therefore, this study was conducted to identify the association between urinary aflatoxin M₁ (AFM₁), a biomarker of aflatoxin exposure, with the dietary intake among adults in Hulu Langat district, Selangor, Malaysia. Certain food products have higher potential for aflatoxin contamination and these were listed in a Food Frequency Questionnaire, which was given to all study participants. This allowed us to record consumption rates for each food product listed. Concomitantly, urine samples were collected, from adults in selected areas in Hulu Langat district, for the measurement of AFM₁ levels using an ELISA kit. Of the 444 urine samples collected and tested, 199 were positive for AFM₁, with 37 of them exceeding the limit of detection (LOD) of 0.64 ng/mL. Cereal products showed the highest consumption level among all food groups, with an average intake of 512.54 g per day. Chi-square analysis showed that consumption of eggs (X² = 4.77, p = 0.03) and dairy products (X² = 19.36, p < 0.01) had significant associations with urinary AFM₁ but both food groups were having a phi and Cramer's V value that less than 0.3, which indicated that the association between these food groups' consumption and AFM₁ level in urine was weak.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.