Sökning: (WFRF:(Ahmad Shafqat)) srt2:(2020-2024) >
Mediterranean Diet ...
-
Ahmad, ShafqatUppsala universitet,Molekylär epidemiologi,Harvard Med Sch, Brigham & Womens Hosp, Ctr Lipid Metabol, 900 Commonwealth Ave,3rd Floor, Boston, MA 02215 USA.;Harvard Med Sch, Brigham & Womens Hosp, Div Prevent Med, Boston, MA USA.
(författare)
Mediterranean Diet Adherence and Risk of All-Cause Mortality in Women
- Artikel/kapitelEngelska2024
Förlag, utgivningsår, omfång ...
-
American Medical Association (AMA),2024
-
electronicrdacarrier
Nummerbeteckningar
-
LIBRIS-ID:oai:DiVA.org:uu-534813
-
https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-534813URI
-
https://doi.org/10.1001/jamanetworkopen.2024.14322DOI
Kompletterande språkuppgifter
-
Språk:engelska
-
Sammanfattning på:engelska
Ingår i deldatabas
Klassifikation
-
Ämneskategori:ref swepub-contenttype
-
Ämneskategori:art swepub-publicationtype
Anmärkningar
-
Importance Higher adherence to the Mediterranean diet has been associated with reduced risk of all-cause mortality, but data on underlying molecular mechanisms over long follow-up are limited. Objectives To investigate Mediterranean diet adherence and risk of all-cause mortality and to examine the relative contribution of cardiometabolic factors to this risk reduction. Design, Setting, and Participants This cohort study included initially healthy women from the Women's Health Study, who had provided blood samples, biomarker measurements, and dietary information. Baseline data included self-reported demographics and a validated food-frequency questionnaire. The data collection period was from April 1993 to January 1996, and data analysis took place from June 2018 to November 2023. Exposures Mediterranean diet score (range, 0-9) was computed based on 9 dietary components. Main Outcome and Measures Thirty-three blood biomarkers, including traditional and novel lipid, lipoprotein, apolipoprotein, inflammation, insulin resistance, and metabolism measurements, were evaluated at baseline using standard assays and nuclear magnetic resonance spectroscopy. Mortality and cause of death were determined from medical and death records. Cox proportional hazards regression was used to calculate hazard ratios (HRs) for Mediterranean diet adherence and mortality risk, and mediation analyses were used to calculate the mediated effect of different biomarkers in understanding this association. Results Among 25 315 participants, the mean (SD) baseline age was 54.6 (7.1) years, with 329 (1.3%) Asian women, 406 (1.6%) Black women, 240 (0.9%) Hispanic women, 24 036 (94.9%) White women, and 95 (0.4%) women with other race and ethnicity; the median (IQR) Mediterranean diet adherence score was 4.0 (3.0-5.0). Over a mean (SD) of 24.7 (4.8) years of follow-up, 3879 deaths occurred. Compared with low Mediterranean diet adherence (score 0-3), adjusted risk reductions were observed for middle (score 4-5) and upper (score 6-9) groups, with HRs of 0.84 (95% CI, 0.78-0.90) and 0.77 (95% CI, 0.70-0.84), respectively (P for trend < .001). Further adjusting for lifestyle factors attenuated the risk reductions, but they remained statistically significant (middle adherence group: HR, 0.92 [95% CI, 0.85-0.99]; upper adherence group: HR, 0.89 [95% CI, 0.82-0.98]; P for trend = .001). Of the biomarkers examined, small molecule metabolites and inflammatory biomarkers contributed most to the lower mortality risk (explaining 14.8% and 13.0%, respectively, of the association), followed by triglyceride-rich lipoproteins (10.2%), body mass index (10.2%), and insulin resistance (7.4%). Other pathways, including branched-chain amino acids, high-density lipoproteins, low-density lipoproteins, glycemic measures, and hypertension, had smaller contributions (<3%). Conclusions and Relevance In this cohort study, higher adherence to the Mediterranean diet was associated with 23% lower risk of all-cause mortality. This inverse association was partially explained by multiple cardiometabolic factors.
Ämnesord och genrebeteckningar
Biuppslag (personer, institutioner, konferenser, titlar ...)
-
Moorthy, M. VinayagaHarvard Med Sch, Brigham & Womens Hosp, Ctr Lipid Metabol, 900 Commonwealth Ave,3rd Floor, Boston, MA 02215 USA.;Harvard Med Sch, Brigham & Womens Hosp, Div Prevent Med, Boston, MA USA.
(författare)
-
Lee, I-MinHarvard Med Sch, Brigham & Womens Hosp, Div Prevent Med, Boston, MA USA.;Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA.
(författare)
-
Ridker, Paul M.Harvard Med Sch, Brigham & Womens Hosp, Div Prevent Med, Boston, MA USA.
(författare)
-
Manson, JoAnn E.Harvard Med Sch, Brigham & Womens Hosp, Div Prevent Med, Boston, MA USA.;Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA.
(författare)
-
Buring, Julie E.Harvard Med Sch, Brigham & Womens Hosp, Div Prevent Med, Boston, MA USA.;Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA.
(författare)
-
Demler, Olga V.Harvard Med Sch, Brigham & Womens Hosp, Ctr Lipid Metabol, 900 Commonwealth Ave,3rd Floor, Boston, MA 02215 USA.;Harvard Med Sch, Brigham & Womens Hosp, Div Prevent Med, Boston, MA USA.;Dept Comp Sci, ETH Zurich, Zurich, Switzerland.
(författare)
-
Mora, SamiaHarvard Med Sch, Brigham & Womens Hosp, Ctr Lipid Metabol, 900 Commonwealth Ave,3rd Floor, Boston, MA 02215 USA.;Harvard Med Sch, Brigham & Womens Hosp, Div Prevent Med, Boston, MA USA.;Harvard Med Sch, Brigham & Womens Hosp, Cardiovasc Div, Boston, MA USA.
(författare)
-
Uppsala universitetMolekylär epidemiologi
(creator_code:org_t)
Sammanhörande titlar
-
Ingår i:JAMA Network Open: American Medical Association (AMA)7:52574-3805
Internetlänk
Hitta via bibliotek
Till lärosätets databas