TY - JOUR
T1 - Association of dietary sulfur amino acid intake with mortality from diabetes and other causes
AU - Dong, Zhen
AU - Gao, Xiang
AU - Chinchilli, Vernon M.
AU - Sinha, Raghu
AU - Muscat, Joshua
AU - Winkels, Renate
AU - Richie, John P.
N1 - Funding Information:
The authors’ responsibilities were as follows: ZD, XG and JPR designed the research, ZD conducted the research and drafted the paper, ZD and VMC analyzed the data and drafted the paper, ZD, XG, JM, RS, RW, and JPR contributed to analysis and manuscript development; and all authors read and approved the final manuscript.
Publisher Copyright:
© 2021, Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2022/2
Y1 - 2022/2
N2 - Purpose: Sulfur amino acid (SAA) consumption in Western countries is far greater than recommended levels. In preclinical studies, reduced SAA intake enhanced longevity and reduced risk for numerous chronic diseases. The current objective was to examine for associations between the intake of total SAA, including methionine (Met) and cysteine (Cys), and all-cause and disease-specific mortality US adults. Methods: This prospective analysis included 15,083 US adult participants (mean age = 46.7 years) from the Third National Examination and Nutritional Health Survey (NHANES III, 1988–1994) with available mortality status (National Death Registry, 1988–2011). Dietary SAA intake was obtained from 24-h recall data. Associations between quintile (Q) of SAA intake (expressed as absolute intake or protein density) and mortality were assessed using Cox proportional hazard models and expressed as hazard ratio (HR). Results: During follow-up (mean = 16.9 years), 4636 deaths occurred. After multivariable adjustment (including demographics and traditional risk factors, such as fat and other micronutrients intake), diabetes-caused mortality rates were nearly threefold higher in the highest compared to lowest SAA intake quintiles [HRQ5–Q1 total SAA, 2.68 (1.46–4.90); HRQ5–Q1 methionine, 2.45 (1.37–4.38); HRQ5–Q1 cysteine, 2.91 (1.57–5.37)] (P < 0.01)]. Higher total SAA protein density was also associated with diabetes-caused mortality [HRQ5–Q1 1.75 (1.31–2.35)]. Associations between SAA intake and all-cause mortality, and mortality caused by other major diseases were not detected. Conclusion: Results suggest that high-SAA diets are associated with increased risk for diabetes mortality and that lowering intake towards to Recommended Dietary Allowance levels could lead to reductions in lifetime risk.
AB - Purpose: Sulfur amino acid (SAA) consumption in Western countries is far greater than recommended levels. In preclinical studies, reduced SAA intake enhanced longevity and reduced risk for numerous chronic diseases. The current objective was to examine for associations between the intake of total SAA, including methionine (Met) and cysteine (Cys), and all-cause and disease-specific mortality US adults. Methods: This prospective analysis included 15,083 US adult participants (mean age = 46.7 years) from the Third National Examination and Nutritional Health Survey (NHANES III, 1988–1994) with available mortality status (National Death Registry, 1988–2011). Dietary SAA intake was obtained from 24-h recall data. Associations between quintile (Q) of SAA intake (expressed as absolute intake or protein density) and mortality were assessed using Cox proportional hazard models and expressed as hazard ratio (HR). Results: During follow-up (mean = 16.9 years), 4636 deaths occurred. After multivariable adjustment (including demographics and traditional risk factors, such as fat and other micronutrients intake), diabetes-caused mortality rates were nearly threefold higher in the highest compared to lowest SAA intake quintiles [HRQ5–Q1 total SAA, 2.68 (1.46–4.90); HRQ5–Q1 methionine, 2.45 (1.37–4.38); HRQ5–Q1 cysteine, 2.91 (1.57–5.37)] (P < 0.01)]. Higher total SAA protein density was also associated with diabetes-caused mortality [HRQ5–Q1 1.75 (1.31–2.35)]. Associations between SAA intake and all-cause mortality, and mortality caused by other major diseases were not detected. Conclusion: Results suggest that high-SAA diets are associated with increased risk for diabetes mortality and that lowering intake towards to Recommended Dietary Allowance levels could lead to reductions in lifetime risk.
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U2 - 10.1007/s00394-021-02641-w
DO - 10.1007/s00394-021-02641-w
M3 - Article
C2 - 34327571
AN - SCOPUS:85111472916
SN - 1436-6207
VL - 61
SP - 289
EP - 298
JO - European Journal of Nutrition
JF - European Journal of Nutrition
IS - 1
ER -