Desmosterol in human nonalcoholic steatohepatitis. Issue 3 (29th July 2013)
- Record Type:
- Journal Article
- Title:
- Desmosterol in human nonalcoholic steatohepatitis. Issue 3 (29th July 2013)
- Main Title:
- Desmosterol in human nonalcoholic steatohepatitis
- Authors:
- Simonen, Marko
Männistö, Ville
Leppänen, Joel
Kaminska, Dorota
Kärjä, Vesa
Venesmaa, Sari
Käkelä, Pirjo
Kuusisto, Johanna
Gylling, Helena
Laakso, Markku
Pihlajamäki, Jussi - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Dysregulation of the cholesterol synthesis pathway and accumulation of cholesterol in the liver are linked to the pathogenesis of nonalcoholic steatohepatitis (NASH). Therefore, we investigated the association of serum and liver levels of cholesterol precursors with NASH. Liver histology was assessed in 110 obese patients (Kuopio Obesity Surgery Study [KOBS] study, age 43.7 ± 8.1 years [mean ± standard deviation, SD], body mass index [BMI] 45.0 ± 6.1 kg/m<sup>2</sup>). Serum and liver levels of cholesterol precursors were measured with gas‐liquid chromatography. The association between cholesterol precursors and serum alanine aminotransferase (ALT), as a marker of liver disease, was also investigated in a population cohort of 717 men (Metabolic Syndrome in Men Study [METSIM] study, age 57.6 ± 5.8 years, BMI 27.1 ± 4.0 kg/m<sup>2</sup>). Serum desmosterol levels and the desmosterol‐to‐cholesterol ratio were higher in individuals with NASH, but not in individuals with simple steatosis, compared to obese subjects with normal liver histology (<italic>P</italic> = 0.002 and <italic>P</italic> = 0.003, respectively). Levels of serum and liver desmosterol correlated strongly (<italic>r</italic> = 0.667, <italic>P</italic> = 1 × 10<sup>−9</sup>), suggesting a shared regulation. Both serum and liver desmosterol levels correlated positively with steatosis and inflammation in the liver<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Dysregulation of the cholesterol synthesis pathway and accumulation of cholesterol in the liver are linked to the pathogenesis of nonalcoholic steatohepatitis (NASH). Therefore, we investigated the association of serum and liver levels of cholesterol precursors with NASH. Liver histology was assessed in 110 obese patients (Kuopio Obesity Surgery Study [KOBS] study, age 43.7 ± 8.1 years [mean ± standard deviation, SD], body mass index [BMI] 45.0 ± 6.1 kg/m<sup>2</sup>). Serum and liver levels of cholesterol precursors were measured with gas‐liquid chromatography. The association between cholesterol precursors and serum alanine aminotransferase (ALT), as a marker of liver disease, was also investigated in a population cohort of 717 men (Metabolic Syndrome in Men Study [METSIM] study, age 57.6 ± 5.8 years, BMI 27.1 ± 4.0 kg/m<sup>2</sup>). Serum desmosterol levels and the desmosterol‐to‐cholesterol ratio were higher in individuals with NASH, but not in individuals with simple steatosis, compared to obese subjects with normal liver histology (<italic>P</italic> = 0.002 and <italic>P</italic> = 0.003, respectively). Levels of serum and liver desmosterol correlated strongly (<italic>r</italic> = 0.667, <italic>P</italic> = 1 × 10<sup>−9</sup>), suggesting a shared regulation. Both serum and liver desmosterol levels correlated positively with steatosis and inflammation in the liver (<italic>P</italic> &lt; 0.05). Serum desmosterol had a higher correlation with the accumulation of cholesterol in the liver than serum cholesterol. Serum desmosterol levels (<italic>P</italic> = 2 × 10<sup>−6</sup>) and the serum desmosterol‐to‐cholesterol ratio (<italic>P</italic> = 5 × 10<sup>−5</sup>) were associated with serum ALT in the population study. <italic>Conclusion</italic>: Levels of desmosterol in serum and the liver were associated with NASH. These results suggest that serum desmosterol is a marker of disturbed cholesterol metabolism in the liver. Whether desmosterol has a more specific role in the pathophysiology of NASH compared to other cholesterol precursors needs to be investigated. (H<sc>epatology</sc> 2013;53:976–982)</p> </abstract> … (more)
- Is Part Of:
- Hepatology. Volume 58:Issue 3(2013:Sep.)
- Journal:
- Hepatology
- Issue:
- Volume 58:Issue 3(2013:Sep.)
- Issue Display:
- Volume 58, Issue 3 (2013)
- Year:
- 2013
- Volume:
- 58
- Issue:
- 3
- Issue Sort Value:
- 2013-0058-0003-0000
- Page Start:
- 976
- Page End:
- 982
- Publication Date:
- 2013-07-29
- Subjects:
- Heart -- Diseases -- Nursing -- Periodicals
Lungs -- Diseases -- Nursing -- Periodicals
Intensive care nursing -- Periodicals
Foie -- Maladies -- Périodiques
616.362 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1527-3350 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/hep.26342 ↗
- Languages:
- English
- ISSNs:
- 0270-9139
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4295.836000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4153.xml