Abnormal regulation of intermediary metabolism after oral glucose ingestion in myotonic dystrophy
- PMID: 2202885
- DOI: 10.1016/0026-0495(90)90304-u
Abnormal regulation of intermediary metabolism after oral glucose ingestion in myotonic dystrophy
Abstract
The responses of plasma insulin and blood intermediary metabolites to oral glucose (75 g) were determined in 10 subjects with myotonic dystrophy. Results were compared with responses in 10 normal control subjects matched for age, sex, and body mass index. Fasting hyperinsulinemia was observed in the myotonic subjects (7.5 +/- 1.6 v 2.4 +/- 0.4 mU/L; P less than .005) and plasma insulin concentration remained significantly higher following oral glucose (F = 38.09; P less than .001). Total cumulative insulin release was markedly higher in the myotonic subjects (4,984.3 v 1,286.6 mU/L; P less than .0001). Basal blood glucose concentration was normal (4.8 +/- 0.2 v 4.7 +/- 0.1 mmol/L), although overall blood glucose was elevated in the myotonic subjects following oral glucose ingestion (F = 5.37; P less than .05). Glucose tolerance was normal in all subjects. Fasting blood lactate was higher in the myotonic subjects (1.31 +/- 0.13 v 0.94 +/- 0.08 mmol/L; P less than .05) and remained significantly elevated following the ingestion of glucose (F = 7.22; P less than .02). Blood pyruvate response was also higher in the myotonic subjects (F = 5.88; P less than .05). Basal blood glycerol was elevated in the myotonic subjects (0.12 +/- 0.02 v 0.05 +/- 0.01 mmol/L; P less than .005) and remained elevated following oral glucose (F = 11.31; P less than .005). No significant overall differences were observed in ketone bodies, alanine, or fatty acids between the groups.(ABSTRACT TRUNCATED AT 250 WORDS)
Similar articles
-
Insulin resistance in multiple aspects of intermediary metabolism in myotonic dystrophy.Metabolism. 1991 Aug;40(8):866-72. doi: 10.1016/0026-0495(91)90017-q. Metabolism. 1991. PMID: 1861635
-
Impaired glucose tolerance is characterized by multiple abnormalities in the regulation of intermediary metabolism.Diabet Med. 1991 Nov;8(9):848-54. doi: 10.1111/j.1464-5491.1991.tb02123.x. Diabet Med. 1991. PMID: 1837511
-
Effect of obesity on circulating intermediary metabolite concentrations in the absence of impaired glucose tolerance.Int J Obes. 1991 Oct;15(10):635-45. Int J Obes. 1991. PMID: 1752724
-
Metabolic abnormalities in obese patients with impaired glucose tolerance.Diabet Med. 1990 Jan;7(1):45-9. doi: 10.1111/j.1464-5491.1990.tb01306.x. Diabet Med. 1990. PMID: 2137062
-
Abnormal regulation of carbohydrate metabolism in motor neurone disease.Diabetes Res. 1991 Feb;16(2):93-9. Diabetes Res. 1991. PMID: 1817811
Cited by
-
RNA metabolism in myotonic dystrophy: patient muscle shows decreased insulin receptor RNA and protein consistent with abnormal insulin resistance.J Clin Invest. 1997 Apr 1;99(7):1691-8. doi: 10.1172/JCI119332. J Clin Invest. 1997. PMID: 9120013 Free PMC article.
-
31P-MRS of skeletal muscle is not a sensitive diagnostic test for mitochondrial myopathy.J Neurol. 2007 Jan;254(1):29-37. doi: 10.1007/s00415-006-0229-5. Epub 2007 Feb 4. J Neurol. 2007. PMID: 17278044
-
Hyperproinsulinaemia in patients with myotonic dystrophy.Diabetologia. 1992 Dec;35(12):1170-2. doi: 10.1007/BF00401372. Diabetologia. 1992. PMID: 1478370
-
Muscleblind-like 3 deficit results in a spectrum of age-associated pathologies observed in myotonic dystrophy.Sci Rep. 2016 Aug 3;6:30999. doi: 10.1038/srep30999. Sci Rep. 2016. PMID: 27484195 Free PMC article.
-
Insulin Signaling as a Key Moderator in Myotonic Dystrophy Type 1.Front Neurol. 2019 Nov 26;10:1229. doi: 10.3389/fneur.2019.01229. eCollection 2019. Front Neurol. 2019. PMID: 31849810 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials