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      Effects of Unfiltered Coffee and Bioactive Coffee Compounds on the Development of Metabolic Syndrome Components in a High-Fat-/High-Fructose-Fed Rat Model

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          Abstract

          The literature is inconsistent as to how coffee affects metabolic syndrome (MetS), and which bioactive compounds are responsible for its metabolic effects. This study aimed to evaluate the effects of unfiltered coffee on diet-induced MetS and investigate whether or not phenolic acids and trigonelline are the main bioactive compounds in coffee. Twenty-four male Sprague‒Dawley rats were fed a high-fat (35% W/W) diet plus 20% W/W fructose in drinking water for 14 weeks, and were randomized into three groups: control, coffee, or nutraceuticals (5- O-caffeoylquinic acid, caffeic acid, and trigonelline). Coffee or nutraceuticals were provided in drinking water at a dosage equal to 4 cups/day in a human. Compared to the controls, total food intake ( p = 0.023) and mean body weight at endpoint ( p = 0.016) and estimated average plasma glucose ( p = 0.041) were lower only in the coffee group. Surrogate measures of insulin resistance including the overall fasting insulin ( p = 0.010), endpoint HOMA-IR ( p = 0.022), and oral glucose tolerance ( p = 0.029) were improved in the coffee group. Circulating triglyceride levels were lower ( p = 0.010), and histopathological and quantitative ( p = 0.010) measurements indicated lower grades of liver steatosis compared to controls after long-term coffee consumption. In conclusion, a combination of phenolic acids and trigonelline was not as effective as coffee per se in improving the components of the MetS. This points to the role of other coffee chemicals and a potential synergism between compounds.

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          Caffeinated and Decaffeinated Coffee Consumption and Risk of Type 2 Diabetes: A Systematic Review and a Dose-Response Meta-analysis

          OBJECTIVE Previous meta-analyses identified an inverse association of coffee consumption with the risk of type 2 diabetes. However, an updated meta-analysis is needed because new studies comparing the trends of association for caffeinated and decaffeinated coffee have since been published. RESEARCH DESIGN AND METHODS PubMed and Embase were searched for cohort or nested case-control studies that assessed the relationship of coffee consumption and risk of type 2 diabetes from 1966 to February 2013. A restricted cubic spline random-effects model was used. RESULTS Twenty-eight prospective studies were included in the analysis, with 1,109,272 study participants and 45,335 cases of type 2 diabetes. The follow-up duration ranged from 10 months to 20 years. Compared with no or rare coffee consumption, the relative risk (RR; 95% CI) for diabetes was 0.92 (0.90–0.94), 0.85 (0.82–0.88), 0.79 (0.75–0.83), 0.75 (0.71–0.80), 0.71 (0.65–0.76), and 0.67 (0.61–0.74) for 1–6 cups/day, respectively. The RR of diabetes for a 1 cup/day increase was 0.91 (0.89–0.94) for caffeinated coffee consumption and 0.94 (0.91–0.98) for decaffeinated coffee consumption (P for difference = 0.17). CONCLUSIONS Coffee consumption was inversely associated with the risk of type 2 diabetes in a dose-response manner. Both caffeinated and decaffeinated coffee was associated with reduced diabetes risk.
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            Scientific Opinion on the safety of caffeine

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              Effect of roasting on the formation of chlorogenic acid lactones in coffee.

              Of all plant constituents, coffee has one of the highest concentrations of chlorogenic acids. When roasting coffee, some of these are transformed into chlorogenic acid lactones (CGL). We have studied the formation of CGL during the roasting of coffee beans in Coffea arabica cv. Bourbon; C. arabicacv. Longberry; and C. canephora cv. Robusta. Individual CGL levels were determined by comparison of HPLC peaks with those of synthetic CGL standards. Seven CGL were identified: 3-caffeoylquinic-1,5-lactone (3-CQL), 4- caffeoylquinic-1,5-lactone (4-CQL), 3-coumaroylquinic-1,5-lactone (3-pCoQL), 4-coumaroylquinic-1,5-lactone (4-pCoQL), 3-feruloylquinic-1,5-lactone (3-FQL), 4-feruloylquinic-1,5-lactone (4-FQL), and 3,4-dicaffeoylquinic-1,5-lactone (3,4-diCQL). 3-CQL was the most abundant lactone in C. arabica and C. canephora, reaching peak values of 230 +/- 9 and 254 +/- 4 mg/100 g (dry weight), respectively, at light medium roast ( approximately 14% weight loss). 4-CQL was the second most abundant lactone (116 +/- 3 and 139 +/- 2 mg/100 g, respectively. The maximum amount of CGL represents approximately 30% of the available precursors. The relative levels of 3-CQL and 4-CQL in roasted coffee were reverse to those of their precursors in green coffee. This suggests that roasting causes isomerization of chlorogenic acids prior to the formation of lactones and that the levels of lactones in roasted coffee do not reflect the levels of precursors in green coffee.
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                Author and article information

                Journal
                Nutrients
                Nutrients
                nutrients
                Nutrients
                MDPI
                2072-6643
                19 October 2018
                October 2018
                : 10
                : 10
                : 1547
                Affiliations
                [1 ]Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Palle Juul Jensens Boulevard 165, 8200 Aarhus N, Denmark; per.bendix.jeppesen@ 123456clin.au.dk (P.B.J.); kjeld.hermansen@ 123456aarhus.rm.dk (K.H.); soeren.gregersen@ 123456aarhus.rm.dk (S.G.)
                [2 ]The Danish Diabetes Academy, Odense University Hospital, Kløvervænget 10, 5000 Odense, Denmark
                [3 ]MR Research Centre, Aarhus University Hospital Skejby, Palle Juul Jensens Boulevard 99, 8200 Aarhus N, Denmark; cl@ 123456clin.au.dk (C.L.); hsj@ 123456clin.au.dk (H.S.-J.); qi@ 123456clin.au.dk (H.Q.); thomasnorlinger@ 123456gmail.com (T.S.N.)
                [4 ]Institute of Pathology, Aarhus University Hospital Skejby, Palle Juul Jensens Boulevard 99, 8200 Aarhus N, Denmark; stephami@ 123456rm.dk
                [5 ]Department of Food Science, Aarhus University, 5792 Årslev, Denmark; mette.schmedes@ 123456food.au.dk
                Author notes
                [* ]Correspondence: Shokouh.P@ 123456Gmail.com ; Tel.: +45-5065-7524
                Author information
                https://orcid.org/0000-0002-4514-0045
                https://orcid.org/0000-0001-8042-7554
                https://orcid.org/0000-0002-0317-2911
                https://orcid.org/0000-0003-3475-8250
                Article
                nutrients-10-01547
                10.3390/nu10101547
                6213813
                30347674
                b336c7da-8486-40cd-950d-d5980e5b3339
                © 2018 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 20 August 2018
                : 11 October 2018
                Categories
                Article

                Nutrition & Dietetics
                coffee,chlorogenic acid,caffeic acid,trigonelline,insulin resistance,metabolic syndrome x,non-alcoholic fatty liver disease,carbon-13 magnetic resonance spectroscopy,phytotherapy

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