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Association between human herpes 8 infection and ketotic type 2 diabetes.


An atypical form of type 2 diabetes type 2 diabetes
n.
See diabetes mellitus.
 that presents with ketosis ketosis /ke·to·sis/ (ke-to´sis) accumulation of excessive amounts of ketone bodies in body tissues and fluids, occurring when fatty acids are incompletely metabolized.ketot´ic

ke·to·sis
n. pl.
 in sub-Saharan blacks has been found to be associated with human herpesvirus 8 (HHV-8), according to a recent paper published in the Journal of the American Medical Association JAMA: The Journal of the American Medical Association is an international peer-reviewed general medical journal, published 48 times per year by the American Medical Association. JAMA is the most widely circulated medical journal in the world. .

Eugene Sobngwi and colleagues carried out a cross-sectional study in which antibodies were searched against latent and lytic lytic /lyt·ic/ (lit´ik)
1. pertaining to lysis or to a lysin.

2. producing lysis.


lyt·ic
adj.
1. Of, relating to, or causing lysis.

2.
 HHV-8 antigens using immunofluorescence. The presence of HHV-8 in genomic DNA was investigated in 22 of the participants at clinical onset of diabetes. They also tested whether HHV-8 was able to infect human pancreatic [beta] cells in culture in vitro. The study was conducted at Saint Louis University Hospital Saint Louis University Hospital is a hospital in St. Louis, Missouri named after Saint Louis, a former French king. Saint Louis University Hospital, also widely known as SLU Hospital, has been owned by the Tenet corporation since the university sold it in 1998. , Paris, France, from January 2004 to July 2005. All participants were black and of African origin: 187 were consecutive diabetic patients of whom 81 had ketosis-prone diabetes mellitus type 2 (DM-2) and 106 had non-ketotic DM-2, and 90 individuals were non-diabetic control participants who were matched for age and sex.

HHV-8 antibodies were found in 71 patients (87.7%) with ketosis-prone DM-2 versus 16 patients (15.1%) with nonketotic DM-2 (odds ratio (OR) 39.9; 95% confidence interval (CI) 17.1-93.4; p<0.001) and 36 of the control participants (40.0%) (OR 10.7; 95% CI 4.9-23.4; p<0.001). HHV-8 in genomic DNA was present in 6 of 13 patients with ketosisprone DM-2 tested at acute onset and in 0 of 9 patients with non-ketotic DM-2. HHV-8 proteins were present in human islet cells that were cultured for 4 days in the presence of HHV-8.

They concluded that the presence of HHV-8 antibodies was associated with ketosisprone DM-2 in patients of sub-Saharan African origin. Longitudinal studies are required to understand the clinical significance of these findings.

Sobngwi E, et al. JAMA JAMA
abbr.
Journal of the American Medical Association
 2008; 299: 2770-2776.
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Title Annotation:Abstracts
Author:Farham, Bridget
Publication:CME: Your SA Journal of CPD
Article Type:Brief article
Geographic Code:6SOUT
Date:Nov 1, 2008
Words:295
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