TY - JOUR
T1 - Dietary sugar intake and risk of Alzheimer's disease in older women
AU - Liu, Longjian
AU - Volpe, Stella L.
AU - Ross, Jennifer A.
AU - Grimm, Jessica A.
AU - Van Bockstaele, Elisabeth J.
AU - Eisen, Howard J.
N1 - Funding Information:
The study was supported by a grant (# 284060, for Dr. L Liu and Dr. S Volpe) from Drexel University Cell2Society Aging Research Network Award, a Drexel Area of Research Excellence (DARE). The study was supported by a grant (# 284060, for Dr. L Liu and Dr. S Volpe) from Drexel University Cell2Society Aging Research Network Award, a Drexel Area of Research Excellence (DARE). This manuscript was prepared using WHICT (WHI-DM), WHIOS Research Materials obtained from the National Heart, Lung, and Blood Institute (NHLBI) Biologic Specimen and Data Repository Information Coordinating Center (NHLBI RMDA# 6820), and does not necessarily reflect the opinions or views of the WHICT (WHI-DM), WHIOS or the NHLBI.
Funding Information:
The study was supported by a grant (# 284060, for Dr. L Liu and Dr. S Volpe) from Drexel University Cell2Society Aging Research Network Award, a Drexel Area of Research Excellence (DARE). This manuscript was prepared using WHICT (WHI-DM), WHIOS Research Materials obtained from the National Heart, Lung, and Blood Institute (NHLBI) Biologic Specimen and Data Repository Information Coordinating Center (NHLBI RMDA# 6820), and does not necessarily reflect the opinions or views of the WHICT (WHI-DM), WHIOS or the NHLBI.
Publisher Copyright:
© 2021 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2022
Y1 - 2022
N2 - Background: Despite some reports of cardiometabolic disorders associated with the risk of Alzheimer's disease (AD), limited studies have been conducted to examine the association between excessive sugar intake (a risk factor for cardiometabolic disorders) and AD risk. Aim: The purpose of our study was to evaluate if excessive sugar intake has a significant long-term effect on the risk of AD. Methods: A population sample of 37,689 participants, who enrolled in the United States (US) Women's Health Initiative–Dietary Modification Trial (WHI-DM) in 1993–2005 and its extended observational follow-up study through 1 March 2019, were analyzed. Dietary sugar intake was measured using food frequency questionnaires. AD was classified by reports using a standard questionnaire. A dietary pattern that explained the maxima variations in sugar intake was constructed using reduced rank regression (RRR) technique. Associations of RRR dietary pattern scores and sugar intake (g/day) by quartiles (Q1 through Q4) with AD risk were examined using Cox proportional hazards regression analysis with adjusting for key covariates. Results: During a mean follow-up of 18.7 years, 4586 participants reported having incident AD. The total incidence rate (95% confidence interval [CI]) of AD was 6.5 (6.3–6.7) per 1000 person-years (PYs). The incidence rates (95% CI) of AD by total sugar intake were 6.2 (5.8–6.6), 6.4 (6.0–6.8), 6.6 (6.3–7.0), and 6.9 (6.5–7.3) per 1000 PYs among those in quartiles (Q) 1 to Q4 (toward higher sugar consumption) of total sugar intake, respectively (test for trend of AD incident rates, p < 0.001). Individuals in Q4 of total sugar intake had a 1.19 higher risk of incident AD than those in Q1 (hazard ratio [HR] = 1.19, 95% CI: 1.05–1.34, p = 0.01). An estimated increase of 10 g/day in total sugar intake (about 2.4 teaspoons) was associated with an increased AD risk by 1.3–1.4%. Of six subtypes of sugar intake, lactose was significantly associated with AD risk. Conclusions: Our study indicates that excessive total sugar intake was significantly associated with AD risk in women. Of six subtypes of sugar intake, lactose had a stronger impact on AD risk.
AB - Background: Despite some reports of cardiometabolic disorders associated with the risk of Alzheimer's disease (AD), limited studies have been conducted to examine the association between excessive sugar intake (a risk factor for cardiometabolic disorders) and AD risk. Aim: The purpose of our study was to evaluate if excessive sugar intake has a significant long-term effect on the risk of AD. Methods: A population sample of 37,689 participants, who enrolled in the United States (US) Women's Health Initiative–Dietary Modification Trial (WHI-DM) in 1993–2005 and its extended observational follow-up study through 1 March 2019, were analyzed. Dietary sugar intake was measured using food frequency questionnaires. AD was classified by reports using a standard questionnaire. A dietary pattern that explained the maxima variations in sugar intake was constructed using reduced rank regression (RRR) technique. Associations of RRR dietary pattern scores and sugar intake (g/day) by quartiles (Q1 through Q4) with AD risk were examined using Cox proportional hazards regression analysis with adjusting for key covariates. Results: During a mean follow-up of 18.7 years, 4586 participants reported having incident AD. The total incidence rate (95% confidence interval [CI]) of AD was 6.5 (6.3–6.7) per 1000 person-years (PYs). The incidence rates (95% CI) of AD by total sugar intake were 6.2 (5.8–6.6), 6.4 (6.0–6.8), 6.6 (6.3–7.0), and 6.9 (6.5–7.3) per 1000 PYs among those in quartiles (Q) 1 to Q4 (toward higher sugar consumption) of total sugar intake, respectively (test for trend of AD incident rates, p < 0.001). Individuals in Q4 of total sugar intake had a 1.19 higher risk of incident AD than those in Q1 (hazard ratio [HR] = 1.19, 95% CI: 1.05–1.34, p = 0.01). An estimated increase of 10 g/day in total sugar intake (about 2.4 teaspoons) was associated with an increased AD risk by 1.3–1.4%. Of six subtypes of sugar intake, lactose was significantly associated with AD risk. Conclusions: Our study indicates that excessive total sugar intake was significantly associated with AD risk in women. Of six subtypes of sugar intake, lactose had a stronger impact on AD risk.
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U2 - 10.1080/1028415X.2021.1959099
DO - 10.1080/1028415X.2021.1959099
M3 - Article
C2 - 34328409
AN - SCOPUS:85111855276
SN - 1028-415X
VL - 25
SP - 2302
EP - 2313
JO - Nutritional Neuroscience
JF - Nutritional Neuroscience
IS - 11
ER -