Angela Kohl
Charité
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Featured researches published by Angela Kohl.
Circulation | 2011
Özlem Gögebakan; Angela Kohl; M Osterhoff; Marleen A. van Baak; Susan A. Jebb; Angeliki Papadaki; J. Alfredo Martínez; Teodora Handjieva-Darlenska; Petr Hlavaty; Martin O. Weickert; Claus Holst; Wim H. M. Saris; Arne Astrup; Andreas F.H. Pfeiffer
Background— We sought to separately examine the effects of either weight loss or diets varying in protein content and glycemic index without further changes in body weight on cardiovascular risk factors within the Diet, Obesity, and Genes study (DiOGenes). Methods and Results— DiOGenes is a pan-European controlled dietary intervention study in 932 overweight adults who first lost body weight on an 8-week low-calorie diet and were then randomized to 1 of 5 ad libitum diets for 26 weeks. The diets were either high or low protein or high or low glycemic index in 4 combinations or control. Weight loss (−11.23 kg; 95% confidence interval, −11.54 to −10.92; P<0.001) reduced high-sensitivity C-reactive protein (−1.15 mg/L; 95% confidence interval, −1.30 to −0.41; P<0.001), low- and high-density lipoprotein cholesterol, triglycerides, and blood pressure. During the 26-week weight maintenance period in the intention-to-treat analysis, the further decrease of high-sensitivity C-reactive protein blood levels was −0.46 mg/L greater (95% confidence interval, −0.79 to −0.13) in the groups assigned to low-glycemic-index diets than in those on high-glycemic-index diets (P<0.001). Groups on low-protein diets achieved a −0.25 mg/L greater reduction in high-sensitivity C-reactive protein (95% confidence interval, −0.59 to −0.17) than those on high-protein diets (P<0.001), whereas lipid profiles and blood pressure were not differently affected. Conclusions— This large-scale intervention study clearly separates weight loss from dietary composition–related effects. Low-glycemic-index carbohydrates and, to a lesser extent, low-protein intake may specifically reduce low-grade inflammation and associated comorbidities in overweight/obese adults. Clinical Trial Registration— http://www.clinicaltrials.gov. Unique identifier: NCT00390637.
The American Journal of Clinical Nutrition | 2011
Martin O. Weickert; Michael Roden; Frank Isken; D Hoffmann; Peter Nowotny; M Osterhoff; Michael Blaut; Carl Alpert; Özlem Gögebakan; Christiane Bumke-Vogt; Friederike Mueller; Jürgen Machann; Thomas M. Barber; Klaus J. Petzke; Johannes Hierholzer; S Hornemann; Michael Kruse; Anne-Kathrin Illner; Angela Kohl; Christian von Loeffelholz; Ayman M. Arafat; Matthias Möhlig; Andreas F.H. Pfeiffer
BACKGROUND Despite their beneficial effects on weight loss and blood lipids, high-protein (HP) diets have been shown to increase insulin resistance and diabetes risk, whereas high-cereal-fiber (HCF) diets have shown the opposite effects on these outcomes. OBJECTIVE We compared the effects of isoenergetic HP and HCF diets and a diet with moderate increases in both cereal fibers and dietary protein (Mix diet) on insulin sensitivity, as measured by using euglycemic-hyperinsulinemic clamps with infusion of [6,6-(2)H(2)]glucose. DESIGN We randomly assigned 111 overweight adults with features of the metabolic syndrome to 1 of 4 two-phased, 18-wk isoenergetic diets by group-matching. Per 3-d food protocols, the percentages of energy derived from protein and carbohydrates and the intake of cereal fiber per day, respectively, were as follows-after 6 wk: 17%, 52%, and 14 g (control); 17%, 52%, and 43 g (HCF); 28%, 43%, and 13 g (HP); 23%, 44%, and 26 g (Mix); after 18 wk: 17%, 51%, and 15 g (control); 17%, 51%, and 41 g (HCF); 26%, 45%, and 14 g (HP); and 22%, 46%, and 26 g (Mix). Eighty-four participants completed the study successfully and were included in the final analyses. Adherence was supported by the provision of tailored dietary supplements twice daily in all groups. RESULTS Insulin sensitivity expressed as an M value was 25% higher after 6 wk of the HCF diet than after 6 wk of the HP diet (subgroup analysis: 4.61 ± 0.38 compared with 3.71 ± 0.36 mg · kg(-1) · min(-1), P = 0.008; treatment × time interaction: P = 0.005). Effects were attenuated after 18 wk (treatment × time interaction: P = 0.054), which was likely explained by lower adherence to the HP diet. HP intake was associated with a tendency to increased protein expression in adipose tissue of the translation initiation factor serine-kinase-6-1, which is known to mediate amino acid-induced insulin resistance. Biomarkers of protein intake indicated interference of cereal fibers with dietary protein absorption. CONCLUSION Greater changes in insulin sensitivity after intake of an isoenergetic HCF than after intake of an HP diet might help to explain the diverse effects of these diets on diabetes risk. This trial is registered at clinicaltrials.gov as NCT00579657.
Obesity Reviews | 2010
C. S. Moore; Anna Karin Lindroos; M. Kreutzer; Thomas Meinert Larsen; Arne Astrup; M. A. van Baak; Teodora Handjieva-Darlenska; Petr Hlavaty; Anthony Kafatos; Angela Kohl; J. A. Martínez; S. Monsheimer; Susan A. Jebb
The aim of this study was to describe the development and implementation of a multifaceted, low‐fat, weight‐loss strategy for a Pan‐European randomized controlled dietary intervention study, Diogenes. There were 891 families with at least one overweight/obese parent who underwent screening. Eligible, overweight/obese adults followed an 8‐week weight‐loss phase with a fixed low‐energy diet (800 kcal). On attaining weight loss of ≥8%, families were randomized to a 6‐ or 12‐month low‐fat (25–30%E) diet either based on national dietary guidelines or one of four interventions: low protein (LP)/low glycaemic index (LGI), LP/high GI (HGI), high protein (HP)/LGI and HP/HGI. The impact of each diet in preventing weight (re)gain was tested. A points‐based system was used to manipulate dietary protein and carbohydrate. Manipulating carbohydrate composition involved substituting foods with a relatively high or low GI. A questionnaire was designed and completed by study investigators, providing feedback on the dietary intervention methods used to inform future interventions. The points system allowed macronutrient manipulations without compromising dietary flexibility or enforcing energy restrictions. Reported centre/participant differences in the ease of implementing the intervention may reflect dietary diversity and personal preferences for specific weight‐management strategies. The points system provides a useful starting point for designing improved experimental paradigms for the manipulation of dietary intake in future trials.
Obesity Reviews | 2010
L. M. Aston; D. Jackson; S. Monsheimer; Stephen Whybrow; Teodora Handjieva-Darlenska; M. Kreutzer; Angela Kohl; Angeliki Papadaki; J. A. Martínez; V. Kunova; M. A. van Baak; Arne Astrup; Wim H. M. Saris; Susan A. Jebb; Anna Karin Lindroos
There is growing evidence that the glycaemic index (GI) of the diet is important with respect to body weight and metabolic disease risk. However, research is limited by the paucity of GI values for commonly consumed carbohydrate‐rich foods in European countries. A new methodology has been developed for consistent assignment of GI values to foods across five European databases used in the Diogenes intervention study. GI values were assigned according to five decreasing levels of confidence (1) Measured values for specific foods; (2) Published values from published sources; (3) Equivalent values where published values for similar foods existed; (4) Estimated values assigned as one of three values representing low/medium/high GI ranges and (5) Nominal values assigned as 70, where no other value could be assigned with sufficient confidence. GI values were assigned to 5105 foods. In food records collected at baseline, the contribution to carbohydrate intake of foods assigned levels 1–2 ranged from 16% to 43% depending on country, and this increased to 53–81% including level 3 foods. The degree of confidence to assigned GI values differed across Europe. This standardized approach of assigning GI values will be made available to other researchers to facilitate further investigation into the effects of dietary GI on health.
Nutrition Research | 2009
Angela Kohl; Özlem Gögebakan; Matthias Möhlig; M Osterhoff; Frank Isken; Andreas F.H. Pfeiffer; Martin O. Weickert
Obesity-induced insulin resistance has been suggested to be a systemic inflammatory condition with activation of the innate immune system. Animal studies indicate that certain dietary fibers such as (1,3)(1,6)-beta-D-glycans (BDG) have potent effects on immune activity such as increasing the antiinflammatory cytokine interleukin-10 (IL-10) and reducing the secretion of inflammatory factors. Therefore, we hypothesized that BDG consumption improves inflammatory markers and insulin sensitivity in overweight and obese subjects with moderately increased levels of C-reactive protein, indicating subclinical inflammation. We screened 180 overweight and obese subjects for moderately increased C-reactive protein levels on 2 or more occasions, in the absence of any signs of acute infection. Twelve of the subjects met all inclusion criteria and were investigated in a randomized, double-blind, placebo-controlled, crossover design for 2 x 4 weeks (washout > or =4 weeks). Subjects ingested capsules containing 3 x 0.5 g of highly purified BDG or 3 x 0.5 g of placebo (waxy maize starch) daily. Maintenance of the normal diet of the participants and the correct intake of the capsules were monitored, using 6 x 3-day food recording and counting of the provided capsules. Predefined outcome measures were BDG-induced changes in pro and antiinflammatory markers in circulating blood and gene expression in adipose tissue and peripheral insulin sensitivity expressed as M value. The BDG consumption for 4 weeks significantly increased both circulating levels and adipose tissue messenger RNA (mRNA) expression of the antiinflammatory cytokine IL-10 in overweight and obese humans. Insulin sensitivity as well as circulating levels and mRNA expression of proinflammatory cytokines were unaffected by BDG treatment. Increased IL-10 after BDG consumption might be a contributing factor to the known beneficial effects of dietary fiber intake.
Circulation | 2011
Özlem Gögebakan; Angela Kohl; M Osterhoff; Marleen A. van Baak; Susan A. Jebb; Angeliki Papadaki; J. Alfredo Martínez; Teodora Handjieva-Darlenska; Petr Hlavaty; Martin O. Weickert; Claus Holst; Wim H. M. Saris; Arne Astrup; Andreas F.H. Pfeiffer
Background— We sought to separately examine the effects of either weight loss or diets varying in protein content and glycemic index without further changes in body weight on cardiovascular risk factors within the Diet, Obesity, and Genes study (DiOGenes). Methods and Results— DiOGenes is a pan-European controlled dietary intervention study in 932 overweight adults who first lost body weight on an 8-week low-calorie diet and were then randomized to 1 of 5 ad libitum diets for 26 weeks. The diets were either high or low protein or high or low glycemic index in 4 combinations or control. Weight loss (−11.23 kg; 95% confidence interval, −11.54 to −10.92; P<0.001) reduced high-sensitivity C-reactive protein (−1.15 mg/L; 95% confidence interval, −1.30 to −0.41; P<0.001), low- and high-density lipoprotein cholesterol, triglycerides, and blood pressure. During the 26-week weight maintenance period in the intention-to-treat analysis, the further decrease of high-sensitivity C-reactive protein blood levels was −0.46 mg/L greater (95% confidence interval, −0.79 to −0.13) in the groups assigned to low-glycemic-index diets than in those on high-glycemic-index diets (P<0.001). Groups on low-protein diets achieved a −0.25 mg/L greater reduction in high-sensitivity C-reactive protein (95% confidence interval, −0.59 to −0.17) than those on high-protein diets (P<0.001), whereas lipid profiles and blood pressure were not differently affected. Conclusions— This large-scale intervention study clearly separates weight loss from dietary composition–related effects. Low-glycemic-index carbohydrates and, to a lesser extent, low-protein intake may specifically reduce low-grade inflammation and associated comorbidities in overweight/obese adults. Clinical Trial Registration— http://www.clinicaltrials.gov. Unique identifier: NCT00390637.
Circulation | 2011
Özlem Gögebakan; Angela Kohl; M Osterhoff; Marleen A. van Baak; Susan A. Jebb; Angeliki Papadaki; J. Alfredo Martínez; Teodora Handjieva-Darlenska; Petr Hlavaty; Martin O. Weickert; Claus Holst; Wim H. M. Saris; Arne Astrup; Andreas F.H. Pfeiffer
Background— We sought to separately examine the effects of either weight loss or diets varying in protein content and glycemic index without further changes in body weight on cardiovascular risk factors within the Diet, Obesity, and Genes study (DiOGenes). Methods and Results— DiOGenes is a pan-European controlled dietary intervention study in 932 overweight adults who first lost body weight on an 8-week low-calorie diet and were then randomized to 1 of 5 ad libitum diets for 26 weeks. The diets were either high or low protein or high or low glycemic index in 4 combinations or control. Weight loss (−11.23 kg; 95% confidence interval, −11.54 to −10.92; P<0.001) reduced high-sensitivity C-reactive protein (−1.15 mg/L; 95% confidence interval, −1.30 to −0.41; P<0.001), low- and high-density lipoprotein cholesterol, triglycerides, and blood pressure. During the 26-week weight maintenance period in the intention-to-treat analysis, the further decrease of high-sensitivity C-reactive protein blood levels was −0.46 mg/L greater (95% confidence interval, −0.79 to −0.13) in the groups assigned to low-glycemic-index diets than in those on high-glycemic-index diets (P<0.001). Groups on low-protein diets achieved a −0.25 mg/L greater reduction in high-sensitivity C-reactive protein (95% confidence interval, −0.59 to −0.17) than those on high-protein diets (P<0.001), whereas lipid profiles and blood pressure were not differently affected. Conclusions— This large-scale intervention study clearly separates weight loss from dietary composition–related effects. Low-glycemic-index carbohydrates and, to a lesser extent, low-protein intake may specifically reduce low-grade inflammation and associated comorbidities in overweight/obese adults. Clinical Trial Registration— http://www.clinicaltrials.gov. Unique identifier: NCT00390637.
Diabetes Care | 2006
Martin O. Weickert; Matthias Möhlig; Christof Schöfl; Ayman M. Arafat; B. Otto; Hannah Viehoff; Corinna Koebnick; Angela Kohl; Joachim Spranger; Andreas F.H. Pfeiffer
Archive | 2015
Angela Kohl; M Osterhoff; Marleen A. van Baak; Susan A. Jebb; Angeliki Papadaki; J. Alfredo Martinez; Teodora Handjieva-Darlenska; Petr Hlavaty; Martin O. Weickert; Claus Holst; Arne Astrup
Diabetologe | 2007
Angela Kohl; Andreas F.H. Pfeiffer
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University Hospitals Coventry and Warwickshire NHS Trust
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