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Hyperglucagonemia in youth is associated with high plasma free fatty acids, visceral adiposity and impaired glucose tolerance

Manell, Hannes (author)
Uppsala universitet,Institutionen för kvinnors och barns hälsa,Institutionen för medicinsk cellbiologi
Kristinsson, Hjalti (author)
Uppsala universitet,Institutionen för medicinsk cellbiologi
Kullberg, Joel, 1979- (author)
Uppsala universitet,Radiologi
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Ubhayasekera, Sarojini Jayantha Kumari (author)
Uppsala universitet,Analytisk kemi
Mörwald, Katharina (author)
Paracelsus Medical University
Staaf, Johan (author)
Uppsala universitet,Institutionen för medicinsk cellbiologi,Institutionen för kvinnors och barns hälsa
Cadamuro, Janne (author)
Paracelsus Medical University
Zsoldos, Fanni (author)
Paracelsus Medical University
Göpel, Sven (author)
AstraZeneca
Sargsyan, Ernest (author)
Uppsala universitet,Institutionen för medicinsk cellbiologi
Ahlström, Håkan, 1953- (author)
Uppsala universitet,Radiologi
Bergquist, Jonas (author)
Uppsala universitet,Analytisk kemi
Weghuber, Daniel (author)
Paracelsus Medical University
Forslund, Anders, 1961- (author)
Uppsala universitet,Pediatrisk inflammationsforskning
Bergsten, Peter (author)
Uppsala universitet,Institutionen för medicinsk cellbiologi,Pediatrisk inflammationsforskning
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 (creator_code:org_t)
2019-07-17
2019
English.
In: Pediatric Diabetes. - : Hindawi Limited. - 1399-543X .- 1399-5448. ; 20:7, s. 880-891
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Objective: To delineate mechanisms for fasting hyperglucagonemia in childhood obesity bystudying the associations between fasting plasma glucagon concentrations and plasmalipid parameters and fat compartments.Methods: Cross-sectional study of children and adolescents with obesity (n=147) and leancontrols (n=43). Differences in free fatty acids (FFA), triglycerides, insulin and fatcompartments (quantified by magnetic resonance imaging) across quartiles of fastingplasma glucagon concentration were analysed. Differences in OGTT glucagonresponse was tested in high vs low FFAs, triglycerides and insulin. Human islets ofLangerhans were cultured at 5.5 mmol/l glucose and in the absence or presence of aFFA mixture with total FFA concentration of 0.5 mmol/l and glucagon secretionquantified.Results: In children with obesity, the quartile with the highest fasting glucagon had higherinsulin (201±174 vs 83±39 pmol/l, p<0.01), FFAs (383±52 vs 338±109 μmol/l,p=0.02), triglycerides (1.5±0.9 vs 1.0±0.7 mmol/l, p<0.01), visceral adipose tissuevolume (1.9±0.8 vs 1.2±0.3 dm3, p<0.001) and a higher prevalence of impairedglucose tolerance (41% vs 8%, p=0.01) than the lowest quartile. During OGTT,children with obesity and high insulin had a worse suppression of glucagon during thefirst 10 minutes after glucose intake. Glucagon secretion was 2.6-fold higher in isletstreated with FFAs than in those not treated with FFAs.4Conclusion: Hyperglucagonemia in childhood obesity is associated with hyperinsulinemia, highplasma FFAs, high plasma triglycerides, visceral adiposity and impaired glucosetolerance. The glucagonotropic effect of FFAs on isolated human islets provides apotential mechanism linking high fasting plasma FFAs and glucagon levels.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Pediatrik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Pediatrics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

Keyword

Childhood obesity
glucagon
free fatty acids
insulin
visceral adiposity
impaired glucose tolerance
type 2 diabetes

Publication and Content Type

ref (subject category)
art (subject category)

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