Association of the Mediterranean Diet With Onset of Diabetes in the Women's Health Study.
Association of the Mediterranean Diet With Onset of Diabetes in the Women's Health Study.
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DOI:
10.1001/jamanetworkopen.2020.25466
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发表时间:
2020-11-02
影响因子:
13.8
通讯作者:
Mora S
中科院分区:
文献类型:
--
作者:
Ahmad S;Demler OV;Sun Q;Moorthy MV;Li C;Lee IM;Ridker PM;Manson JE;Hu FB;Fall T;Chasman DI;Cheng S;Pradhan A;Mora S
Is the Mediterranean (MED) diet associated with reduced risk of diabetes in a US population, and if so, what are possible underlying biological mechanistic pathways? Among 25 317 women followed up for 20 years in a prospective epidemiological cohort study, 2307 developed type 2 diabetes. Higher baseline MED intake was associated with a 30% reduction in future risk of diabetes; biomarkers of insulin resistance, adiposity, high-density lipoprotein, and inflammation contributed most to explaining this inverse association. These findings suggest that the MED diet may be protective against diabetes by improving insulin resistance, lipoprotein metabolism, and inflammation. This cohort study characterizes the relative association of conventional and novel biomarkers in Mediterranean diet–related type 2 diabetes risk reduction in a US population. Higher Mediterranean diet (MED) intake has been associated with reduced risk of type 2 diabetes, but underlying biological mechanisms are unclear. To characterize the relative contribution of conventional and novel biomarkers in MED-associated type 2 diabetes risk reduction in a US population. This cohort study was conducted among 25 317 apparently healthy women. The participants with missing information regarding all traditional and novel metabolic biomarkers or those with baseline diabetes were excluded. Participants were invited for baseline assessment between September 1992 and May 1995. Data were collected from November 1992 to December 2017 and analyzed from December 2018 to December 2019. MED intake score (range, 0 to 9) was computed from self-reported dietary intake, representing adherence to Mediterranean diet intake. Incident cases of type 2 diabetes, identified through annual questionnaires; reported cases were confirmed by either telephone interview or supplemental questionnaire. Proportion of reduced risk of type 2 diabetes explained by clinical risk factors and a panel of 40 biomarkers that represent different physiological pathways was estimated. The mean (SD) age of the 25 317 female participants was 52.9 (9.9) years, and they were followed up for a mean (SD) of 19.8 (5.8) years. Higher baseline MED intake (score ≥6 vs ≤3) was associated with as much as a 30% lower type 2 diabetes risk (age-adjusted and energy-adjusted hazard ratio, 0.70; 95% CI, 0.62-0.79; when regression models were additionally adjusted with body mass index [BMI]: hazard ratio, 0.85; 95% CI, 0.76-0.96). Biomarkers of insulin resistance made the largest contribution to lower risk (accounting for 65.5% of the MED–type 2 diabetes association), followed by BMI (55.5%), high-density lipoprotein measures (53.0%), and inflammation (52.5%), with lesser contributions from branched-chain amino acids (34.5%), very low-density lipoprotein measures (32.0%), low-density lipoprotein measures (31.0%), blood pressure (29.0%), and apolipoproteins (23.5%), and minimal contribution (≤2%) from hemoglobin A1c. In post hoc subgroup analyses, the inverse association of MED diet with type 2 diabetes was seen only among women who had BMI of at least 25 at baseline but not those who had BMI of less than 25 (eg, women with BMI <25, age- and energy-adjusted HR for MED score ≥6 vs ≤3, 1.01; 95% CI, 0.77-1.33; P for trend = .92; women with BMI ≥25: HR, 0.76; 95% CI, 0.67-0.87; P for trend < .001). In this cohort study, higher MED intake scores were associated with a 30% relative risk reduction in type 2 diabetes during a 20-year period, which could be explained in large part by biomarkers of insulin resistance, BMI, lipoprotein metabolism, and inflammation.
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影响因子:
7.6
作者:
BARON, RM;KENNY, DA
通讯作者:
KENNY, DA
影响因子:
16.2
作者:
de Koning L;Chiuve SE;Fung TT;Willett WC;Rimm EB;Hu FB
通讯作者:
Hu FB
影响因子:
105.7
作者:
Martinez-Gonzalez, M. A.;de la Fuente-Arrillaga, C.;Bes-Rastrollo, M.
通讯作者:
Bes-Rastrollo, M.
影响因子:
13.8
作者:
Ahmad, Shafqat;Moorthy, M. Vinayaga;Mora, Samia
通讯作者:
Mora, Samia
影响因子:
7.7
作者:
Howe LD;Smith AD;Macdonald-Wallis C;Anderson EL;Galobardes B;Lawlor DA;Ben-Shlomo Y;Hardy R;Cooper R;Tilling K;Fraser A
通讯作者:
Fraser A