13 results on '"Hammarstedt, Ann"'
Search Results
2. Adipose tissue morphology, imaging and metabolomics predicting cardiometabolic risk and family history of type 2 diabetes in non-obese men.
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Rawshani, Aidin, Eliasson, Björn, Rawshani, Araz, Henninger, Josefin, Mardinoglu, Adil, Carlsson, Åsa, Sohlin, Maja, Ljungberg, Maria, Hammarstedt, Ann, Rosengren, Annika, and Smith, Ulf
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ADIPOSE tissues ,METABOLOMICS ,TYPE 2 diabetes ,BIOMARKERS ,MACHINE learning - Abstract
We evaluated the importance of body composition, amount of subcutaneous and visceral fat, liver and heart ectopic fat, adipose tissue distribution and cell size as predictors of cardio-metabolic risk in 53 non-obese male individuals. Known family history of type 2 diabetes was identified in 25 individuals. The participants also underwent extensive phenotyping together with measuring different biomarkers and non-targeted serum metabolomics. We used ensemble learning and other machine learning approaches to identify predictors with considerable relative importance and their intricate interactions. Visceral fat and age were strong individual predictors of ectopic fat accumulation in liver and heart along with markers of lipid oxidation and reduced glucose tolerance. Subcutaneous adipose cell size was the strongest individual predictor of whole-body insulin sensitivity and also a marker of visceral and ectopic fat accumulation. The metabolite 3-MOB along with related branched-chain amino acids demonstrated strong predictability for family history of type 2 diabetes. [ABSTRACT FROM AUTHOR]
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- 2020
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3. The Novel Adipokine Gremlin 1 Antagonizes Insulin Action and Is Increased in Type 2 Diabetes and NAFLD/NASH.
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Hedjazifar, Shahram, Shahidi, Roxana Khatib, Hammarstedt, Ann, Bonnet, Laurianne, Church, Christopher, Boucher, Jeremie, Blüher, Matthias, Smith, Ulf, and Khatib Shahidi, Roxana
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TYPE 2 diabetes ,CHEMERIN ,FAT cells ,INSULIN ,LIVER cells ,FATTY liver ,RNA metabolism ,ADIPOSE tissues ,CELL culture ,COMPARATIVE studies ,EPITHELIAL cells ,GROWTH factors ,HORMONE antagonists ,INSULIN resistance ,LIVER ,RESEARCH methodology ,MEDICAL cooperation ,OBESITY ,PEPTIDE hormones ,RESEARCH ,EVALUATION research ,CASE-control method ,SKELETAL muscle ,GLUCOSE clamp technique - Abstract
The BMP2/4 antagonist and novel adipokine Gremlin 1 is highly expressed in human adipose cells and increased in hypertrophic obesity. As a secreted antagonist, it inhibits the effect of BMP2/4 on adipose precursor cell commitment/differentiation. We examined mRNA levels of Gremlin 1 in key target tissues for insulin and also measured tissue and serum levels in several carefully phenotyped human cohorts. Gremlin 1 expression was high in adipose tissue, higher in visceral than in subcutaneous tissue, increased in obesity, and further increased in type 2 diabetes (T2D). A similar high expression was seen in liver biopsies, but expression was considerably lower in skeletal muscles. Serum levels were increased in obesity but most prominently in T2D. Transcriptional activation in both adipose tissue and liver as well as serum levels were strongly associated with markers of insulin resistance in vivo (euglycemic clamps and HOMA of insulin resistance), and the presence of nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH). We also found Gremlin 1 to antagonize insulin signaling and action in human primary adipocytes, skeletal muscle, and liver cells. Thus, Gremlin 1 is a novel secreted insulin antagonist and biomarker as well as a potential therapeutic target in obesity and its complications T2D and NAFLD/NASH. [ABSTRACT FROM AUTHOR]
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- 2020
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4. IMPAIRED ADIPOGENESIS AND DYSFUNCTIONAL ADIPOSE TISSUE IN HUMAN HYPERTROPHIC OBESITY.
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Hammarstedt, Ann, Gogg, Silvia, Hedjazifar, Shahram, Nerstedt, Annika, and Smith, Ulf
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ADIPOSE tissues , *OBESITY , *INSULIN resistance , *METABOLIC disorders , *ADIPONECTIN - Abstract
The subcutaneous adipose tissue (SAT) is the largest and best storage site for excess lipids. However, it has a limited ability to expand by recruiting and/or differentiating available precursor cells. When inadequate, this leads to a hypertrophic expansion of the cells with increased inflammation, insulin resistance, and a dysfunctional prolipolytic tissue. Epi-/genetic factors regulate SAT adipogenesis and genetic predisposition for type 2 diabetes is associated with markers of an impaired SAT adipogenesis and development of hypertrophic obesity also in nonobese individuals. We here review mechanisms for the adipose precursor cells to enter adipogenesis, emphasizing the role of bone morphogenetic protein-4 (BMP-4) and its endogenous antagonist gremlin-1, which is increased in hypertrophic SAT in humans. Gremlin-1 is a secreted and a likely important mechanism for the impaired SAT adipogenesis in hypertrophic obesity. Transiently increasing BMP-4 enhances adipogenic commitment of the precursor cells while maintained BMP-4 signaling during differentiation induces a beige/brown oxidative phenotype in both human and murine adipose cells. Adipose tissue growth and development also requires increased angiogenesis, and BMP-4, as a proangiogenic molecule, may also be an important feedback regulator of this. Hypertrophic obesity is also associated with increased lipolysis. Reduced lipid storage and increased release of FFA by hypertrophic SAT are important mechanisms for the accumulation of ectopic fat in the liver and other places promoting insulin resistance. Taken together, the limited expansion and storage capacity of SAT is a major driver of the obesity-associated metabolic complications. [ABSTRACT FROM AUTHOR]
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- 2018
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5. Increased adipose tissue aromatase activity improves insulin sensitivity and reduces adipose tissue inflammation in male mice.
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Ohlsson, Claes, Hammarstedt, Ann, Vandenput, Liesbeth, Saarinen, Niina, Ryberg, Henrik, Windahl, Sara H., Farman, Helen H., Jansson, John-Olov, Movérare-Skrtic, Sofia, Smith, Ulf, Fu-Ping Zhang, Poutanen, Matti, Hedjazifar, Shahram, and Sjögren, Klara
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INFLAMMATION treatment , *ADIPOSE tissues , *AROMATASE inhibitors , *INSULIN resistance , *LABORATORY mice , *GENE expression - Abstract
Females are, in general, more insulin sensitive than males. To investigate whether this is a direct effect of sex-steroids (SS) in white adipose tissue (WAT), we developed a male mouse model overexpressing the aromatase enzyme, converting testosterone (T) to estradiol (E2), specifically in WAT (Ap2-arom mice). Adipose tissue E2 levels were increased while circulating SS levels were unaffected in male Ap2-arom mice. Importantly, male Ap2-arom mice were more insulin sensitive compared with WT mice and exhibited increased serum adiponectin levels and upregulated expression of Glut4 and Irs1 in WAT. The expression of markers of macrophages and immune cell infiltration was markedly decreased in WAT of male Ap2-arom mice. The adipogenesis was enhanced in male Ap2-arom mice, supported by elevated Pparg expression in WAT and enhanced differentiation of preadipocyte into mature adipocytes. In summary, increased adipose tissue aromatase activity reduces adipose tissue inflammation and improves insulin sensitivity in male mice. We propose that estrogen increases insulin sensitivity via a local effect in WAT on adiponectin expression, adipose tissue inflammation, and adipogenesis. [ABSTRACT FROM AUTHOR]
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- 2017
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6. BMP4 and BMP Antagonists Regulate Human White and Beige Adipogenesis.
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Gustafson, Birgit, Hammarstedt, Ann, Hedjazifar, Shahram, Hoffmann, Jenny M., Svensson, Per-Arne, Grimsby, Joseph, Rondinone, Cristina, and Smith, Ulf
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ADIPOSE tissues , *FAT cells , *ADIPOGENESIS , *OBESITY , *BONE morphogenetic proteins , *PHENOTYPES - Abstract
The limited expandability of subcutaneous adipose tissue, due to reduced ability to recruit and differentiate new adipocytes, prevents its buffering effect in obesity and is characterized by expanded adipocytes (hypertrophic obesity). Bone morphogenetic protein-4 (BMP4) plays a key role in regulating adipogenic precursor cell commitment and differentiation. We found BMP4 to be induced and secreted by differentiated (pre)adipocytes, and BMP4 was increased in large adipose cells. However, the precursor cells exhibited a resistance to BMP4 owing to increased secretion of the BMP inhibitor Gremlin-1 (GREM1). GREM1 is secreted by (pre)adipocytes and is an inhibitor of both BMP4 and BMP7. BMP4 alone, and/or silencing GREM1, increased transcriptional activation of peroxisome proliferator-activated receptor g and promoted the preadipocytes to assume an oxidative beige/brown adipose phenotype including markers of increased mitochondria and PGC1α. Driving white adipose differentiation inhibited the beige/brown markers, suggesting the presence of multipotent adipogenic precursor cells. However, silencing GREM1 and/or adding BMP4 during white adipogenic differentiation reactivated beige/brown markers, suggesting that increased BMP4 preferentially regulates the beige/brown phenotype. Thus, BMP4, secreted by white adipose cells, is an integral feedback regulator of both white and beige adipogenic commitment and differentiation, and resistance to BMP4 by GREM1 characterizes hypertrophic obesity. [ABSTRACT FROM AUTHOR]
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- 2015
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7. Adipocyte Hypertrophy, Inflammation and Fibrosis Characterize Subcutaneous Adipose Tissue of Healthy, Non-Obese Subjects Predisposed to Type 2 Diabetes.
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Henninger, A. M. Josefin, Eliasson, Björn, Jenndahl, Lachmi E., and Hammarstedt, Ann
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FAT cells ,HYPERTROPHY ,CIRRHOSIS of the liver ,ADIPOSE tissues ,TYPE 2 diabetes ,INSULIN resistance ,GENE expression - Abstract
Background: The adipose tissue is important for development of insulin resistance and type 2 diabetes and adipose tissue dysfunction has been proposed as an underlying cause. In the present study we investigated presence of adipocyte hypertrophy, and gene expression pattern of adipose tissue dysfunction in the subcutaneous adipose tissue of healthy, non-obese subjects predisposed to type 2 diabetes compared to matched control subjects with no known genetic predisposition for type 2 diabetes. Method: Seventeen healthy and non-obese subjects with known genetic predisposition for type 2 diabetes (first-degree relatives, FDRs) and 17 control subjects were recruited. The groups were matched for gender and BMI and had similar age. Glucose tolerance was determined by an oral glucose tolerance test and insulin sensitivity was calculated using HOMA-index. Blood samples were collected and subcutaneous abdominal adipose tissue biopsies obtained for gene expression analysis and adipocyte cell size measurement. Results: Our findings show that, in spite of similar age, BMI and percent body fat, FDRs displayed adipocyte hypertrophy, as well as higher waist/hip ratio, fasting insulin levels, HOMA-IR and serum triglycerides. Adipocyte hypertrophy in the FDR group, but not among controls, was associated with measures of impaired insulin sensitivity. The adipocyte hypertrophy was accompanied by increased inflammation and Wnt-signal activation. In addition, signs of tissue remodeling and fibrosis were observed indicating presence of early alterations associated with adipose tissue dysfunction in the FDRs. Conclusion: Genetic predisposition for type 2 diabetes is associated with impaired insulin sensitivity, adipocyte hypertrophy and other markers of adipose tissue dysfunction. A dysregulated subcutaneous adipose tissue may be a major susceptibility factor for later development of type 2 diabetes. [ABSTRACT FROM AUTHOR]
- Published
- 2014
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8. Restricted Adipogenesis in Hypertrophic Obesity.
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Gustafson, Birgit, Hammarstedt, Ann, Hedjazifar, Shahram, and Smith, Ulf
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ADIPOSE tissues , *OBESITY , *CELLS , *METABOLIC disorders , *HYPERTROPHY - Abstract
The article discusses the limited expandability of the subcutaneous adipose tissue which may lead to inappropriate cell expansion associated with hypertrophic obesity. The authors explain that hypertrophic obesity is basically an impaired ability to recruit and differentiate available adipose precursor cells in the subcutaneous adipose tissue. They assert that this inability results in lipid overflow and ectopic fat accumulation, coupled with negative metabolic consequences.
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- 2013
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9. Genetic Predisposition for Type 2 Diabetes, but Not for Overweight/Obesity, Is Associated with a Restricted Adipogenesis.
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Arner, Peter, Arner, Erik, Hammarstedt, Ann, and Smith, Ulf
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TYPE 2 diabetes ,OBESITY ,HUMAN genetic variation ,ADIPOSE tissues ,BIOPSY ,INSULIN shock ,METABOLIC syndrome - Abstract
Background: Development of Type 2 diabetes, like obesity, is promoted by a genetic predisposition. Although several genetic variants have been identified they only account for a small proportion of risk. We have asked if genetic risk is associated with abnormalities in storing excess lipids in the abdominal subcutaneous adipose tissue. Methodology/Principal Findings: We recruited 164 lean and 500 overweight/obese individuals with or without a genetic predisposition for Type 2 diabetes or obesity. Adipose cell size was measured in biopsies from the abdominal adipose tissue as well as insulin sensitivity (HOMA index), HDL-cholesterol and Apo AI and Apo B. 166 additional non-obese individuals with a genetic predisposition for Type 2 diabetes underwent a euglycemic hyperinsulinemic clamp to measure insulin sensitivity. Genetic predisposition for Type 2 diabetes, but not for overweight/obesity, was associated with inappropriate expansion of the adipose cells, reduced insulin sensitivity and a more proatherogenic lipid profile in non-obese individuals. However, obesity per se induced a similar expansion of adipose cells and dysmetabolic state irrespective of genetic predisposition. Conclusions/Significance: Genetic predisposition for Type 2 diabetes, but not obesity, is associated with an impaired ability to recruit new adipose cells to store excess lipids in the subcutaneous adipose tissue, thereby promoting ectopic lipid deposition. This becomes particularly evident in non-obese individuals since obesity per se promotes a dysmetabolic state irrespective of genetic predisposition. These results identify a novel susceptibility factor making individuals with a genetic predisposition for Type 2 diabetes particularly sensitive to the environment and caloric excess. [ABSTRACT FROM AUTHOR]
- Published
- 2011
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10. Antagonistic effects of thiazolidinediones and cytokines in lipotoxicity
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Smith, Ulf and Hammarstedt, Ann
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CYTOKINES , *TOXICOLOGY , *LIPID metabolism , *TRIGLYCERIDES , *ADIPOSE tissues , *OBESITY , *FAT cells , *INFLAMMATION , *TUMOR necrosis factors - Abstract
Abstract: Ectopic lipid accumulation is promoted by obesity and an impaired ability to accumulate triglycerides in the subcutaneous depots. The adipose tissue is dysregulated in hypertrophic obesity, i.e., when the adipose cells have become enlarged. In some individuals, however, obesity is a consequence of a recruitment of new adipocytes, i.e., a hyperplastic obesity. This form of obesity is usually not associated with the metabolic complications and is termed “obese but metabolically normal”. We here review recent findings showing that hypertrophic obesity is associated with an impaired differentiation of committed preadipocytes. This may be a primary (genetic?) event, thus leading to hypertrophic fat cells and the associated inflammation. However, it is also possible that the inflammation is a primary event allowing, in particular, TNFα to inhibit preadipocyte differentiation. TNFα, instead, promotes a partial transdifferentiation of the preadipocytes to assume a macrophage-like phenotype. PPARγ activation promotes adipogenesis but can apparently not overcome the impaired preadipocyte differentiation seen in hypertrophic obesity. [Copyright &y& Elsevier]
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- 2010
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11. A novel cellular marker of insulin resistance and early atherosclerosis in humans is related to impaired fat cell differentiation and low adiponectin.
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Jansson, Per-Anders, Pellme, Fredrik, Hammarstedt, Ann, Sandqvist, Madelene, Brekke, Hilde, Caidahl, Kenneth, Forsberg, Margareta, Volkman, Reinhard, Carvalho, Eugenia, Funahashi, Tohru, Matsuzawa, Yuji, Wiklund, Olle, Yang, Xiaolin, Taskinen, Marja-Riitta, and Smith, Ulf
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PHENOTYPES ,INSULIN receptors ,FAT cells ,ADIPOSE tissues ,CONNECTIVE tissues - Abstract
Provides information on a study that examined the clinical phenotype of individuals characterized by normal or low insulin receptor substrate-1 protein expression in fat cells as well as the potential molecular mechanisms related to the adipose tissue. Methodology of the study; Results and discussion on the study.
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- 2003
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12. Discovery of a Class of Endogenous Mammalian Lipids with Anti-Diabetic and Anti-inflammatory Effects.
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Yore, Mark M., Syed, Ismail, Moraes-Vieira, Pedro M., Zhang, Tejia, Herman, Mark A., Homan, Edwin A., Patel, Rajesh T., Lee, Jennifer, Chen, Shili, Peroni, Odile D., Dhaneshwar, Abha S., Hammarstedt, Ann, Smith, Ulf, McGraw, Timothy E., Saghatelian, Alan, and Kahn, Barbara B.
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ADIPOSE tissues , *LIPID synthesis , *INSULIN resistance , *HYPOGLYCEMIC agents , *ANTI-inflammatory agents , *GLUCOSE transporters , *LABORATORY mice - Abstract
Summary Increased adipose tissue lipogenesis is associated with enhanced insulin sensitivity. Mice overexpressing the Glut4 glucose transporter in adipocytes have elevated lipogenesis and increased glucose tolerance despite being obese with elevated circulating fatty acids. Lipidomic analysis of adipose tissue revealed the existence of branched f atty a cid esters of h ydroxy f atty a cids (FAHFAs) that were elevated 16- to 18-fold in these mice. FAHFA isomers differ by the branched ester position on the hydroxy fatty acid (e.g., p almitic- a cid-9- h ydroxy- s tearic- a cid, 9-PAHSA). PAHSAs are synthesized in vivo and regulated by fasting and high-fat feeding. PAHSA levels correlate highly with insulin sensitivity and are reduced in adipose tissue and serum of insulin-resistant humans. PAHSA administration in mice lowers ambient glycemia and improves glucose tolerance while stimulating GLP-1 and insulin secretion. PAHSAs also reduce adipose tissue inflammation. In adipocytes, PAHSAs signal through GPR120 to enhance insulin-stimulated glucose uptake. Thus, FAHFAs are endogenous lipids with the potential to treat type 2 diabetes. [ABSTRACT FROM AUTHOR]
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- 2014
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13. Adipokines, systemic inflammation and inflamed adipose tissue in obesity and insulin resistance
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Smith, Ulf, Andersson, Christian X., Gustafson, Birgit, Hammarstedt, Ann, Isakson, Petter, and Wallerstedt, Emelie
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OBESITY , *ADIPOSE tissues , *FAT cells , *INSULIN resistance - Abstract
Abstract: Obesity and its complications are characterized by elevated circulating levels of inflammation markers like CRP, IL-6 and serum amyloid A. Although several cells secrete these markers, the adipose tissue seems to play a pivotal role for the proinflammatory state. Obesity with enlarged adipose cells leads to a marked increase in the expression of pro-inflammatory cytokines in the adipose tissue while expression of the anti-inflammatory adipokine, adiponectin, is reduced. The mechanisms for this are currently unknown but a consequence is the recruitment of inflammatory cells into the adipose tissue which, thus, becomes inflamed. Animal experiments have shown that this is associated with a clear accentuation of degree of insulin resistance. Invasion of inflammatory cells leads to the release of TNFa, which normally is not secreted by the adipose cells. The increased levels of cytokines in the adipose tissue have marked consequences for the normal differentiation of the preadipocytes. These cells become proinflammatory and the normal phenotype, i.e., lipid-accumulating and insulin-sensitive cells, is suppressed. Although inflammation in the adipose tissue also leads to a reduced insulin sensitivity, recent data have shown that induction of insulin resistance by itself in the adipose tissue also is proinflammatory since insulin can exert an anti-inflammatory effect through its cross-talk with the IL-6 signaling cascade. [Copyright &y& Elsevier]
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- 2007
- Full Text
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