PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
July 1, 2002The Journal of Clinical Endocrinology & Metabolism1,078 citations

Fat Accumulation in the Liver Is Associated with Defects in Insulin Suppression of Glucose Production and Serum Free Fatty Acids Independent of Obesity in Normal Men

View Full Paper
ASAnneli Seppälä‐LindroosSVSatu VehkavaaraAHAnna‐Maija Häkkinen

Key Points

  • To determine whether variations in liver fat content alter hepatic insulin sensitivity and lipid regulation independently of overall and abdominal obesity in healthy men.
  • Recruited N=30 healthy nondiabetic men stratified into low (1.7 ± 0.2%) and high (10.5 ± 2.0%) liver fat content (LFAT) groups based on proton spectroscopy measurements.
  • Quantified intraabdominal, subcutaneous, and total body fat using magnetic resonance imaging (MRI).
  • Evaluated insulin-mediated suppression of endogenous glucose production rate (Ra) and serum free fatty acids (FFA) via a euglycemic-hyperinsulinemic clamp combined with [3-3H]glucose infusion.
  • Insulin-induced suppression of endogenous glucose production was significantly impaired in the high versus low LFAT group (-55 ± 7% vs. -85 ± 12% below basal; P < 0.05), as was suppression of serum free fatty acids (299 ± 33 vs. 212 ± 13 µmol/L; P < 0.02), despite identical BMI and abdominal fat volumes.
  • High LFAT subjects displayed markers of metabolic dysfunction, including fasting hyperinsulinemia (7.3 ± 0.6 vs. 5.3 ± 0.6 mU/L; P < 0.02), hypertriglyceridemia (1.4 ± 0.2 vs. 0.9 ± 0.1 mmol/L; P < 0.02), lower HDL cholesterol (1.4 ± 0.1 vs. 1.6 ± 0.1 mmol/L; P < 0.05), and higher 24-hour systolic blood pressure (130 ± 3 vs. 122 ± 3 mm Hg; P < 0.05).

Abstract

We determined whether interindividual variation in hepatic insulin sensitivity could be attributed to variation in liver fat content (LFAT) independent of obesity. We recruited 30 healthy nondiabetic men whose LFAT (determined by proton spectroscopy); intraabdominal, sc, and total (determined by magnetic resonance imaging) fat; and insulin sensitivity of endogenous glucose rate of production (R(a)) and suppression of serum FFA euglycemic insulin clamp combined with [3-(3)Hglucose (0-300 min); insulin infusion rate, 0.3 mU/kg.min, 120-300 min] were measured. The men were divided into groups of low (mean +/- SD, 1.7 +/- 0.2%) and high (10.5 +/- 2.0%) LFAT based on their median fat content. The low and high LFAT groups were comparable with respect to age (44 +/- 2 vs. 42 +/- 2 yr), body mass index (25 +/- 1 vs. 26 +/- 1 kg/m(2) ), waist to hip ratio (0.953 +/- 0.013 vs. 0.953 +/- 0.013), maximal oxygen uptake (35.6 +/- 1.5 vs. 33.5 +/- 1.5 ml/kg.min), and intraabdominal, sc, and total fat. The high compared with the low LFAT group had several features of insulin resistance, including fasting hyperinsulinemia (7.3 +/- 0.6 vs. 5.3 +/- 0.6 mU/liter; P < 0.02, high vs. low LFAT) hypertriglyceridemia (1.4 +/- 0.2 vs. 0.9 +/- 0.1 mmol/liter; P < 0.02), a low high density lipoprotein (HDL) cholesterol concentration (1.4 +/- 0.1 vs. 1.6 +/- 0.1 mmol/liter; P < 0.05), and a higher ambulatory 24-h systolic blood pressure (130 +/- 3 vs. 122 +/- 3 mm Hg; P < 0.05). Basal glucose R(a) and serum FFA were comparable between the groups, whereas insulin suppression of glucose R(a) 51 +/- 8 vs. 20 +/- 12 mg/m(2).min during 240-300 min (P < 0.05) or -55 +/- 7 vs. -85 +/- 12% below basal (P < 0.05, high vs. low LFAT) and of serum FFA (299 +/- 33 vs. 212 +/- 13 micromol/liter; 240-300 min; P < 0.02) were impaired in the high compared with the low LFAT group. Insulin stimulation of glucose Rd were comparable in the men with high LFAT (141 +/- 12 mg/m(2).min) and those with low LFAT (156 +/- 14 mg/m(2).min; P = NS). Fat accumulation in the liver is, independent of body mass index and intraabdominal and overall obesity, characterized by several features of insulin resistance in normal weight and moderately overweight subjects.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Seppälä‐Lindroos et al. (2002) studied this question.

synapsesocial.com/papers/6a180c227c70e6dd4312a217https://doi.org/10.1210/jcem.87.7.8638
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Glucose clamp technique: a method for quantifying insulin secretion and resistance.1979 · 7,479 citations
  2. 2Visceral fat and insulin resistance — causative or correlative?2000 · 448 citations
  3. 3Loss of Insulin Signaling in Hepatocytes Leads to Severe Insulin Resistance and Progressive Hepatic Dysfunction2000 · 224 citations
  4. 4Troglitazone action is independent of adipose tissue.1997 · 339 citations
  5. 5Nonalcoholic steatohepatitis: An expanded clinical entity1993 · 90 citations