Circulating Antibodies to Cardiac Protein—Acetaldehyde Adducts in Alcoholic Heart Muscle Disease

1995 ◽  
Vol 88 (3) ◽  
pp. 263-268 ◽  
Author(s):  
A. A. Harcombe ◽  
L. Ramsay ◽  
J. G. Kenna ◽  
J. Koskinas ◽  
H. J. F. Why ◽  
...  

1. Serum samples from patients with alcoholic heart muscle disease and from control subjects with and without heart disease who did not drink to excess were screened by Western immunoblotting for antibodies to acetaldehyde-modified cardiac cytosolic proteins. 2. Two of the 64 control samples (from subjects with and without heart disease who were not drinking and from subjects with alcoholic liver disease) had detectable (IgG) antibody to acetaldehyde-modified cardiac proteins. 3. By contrast, 7 of 21 (33%) patients with alcoholic heart muscle disease had antibodies against cyanoborohydride-stabilized, acetaldehyde-modified human cardiac cytosolic protein antigens (P < 0.001). 4. Antibodies were of IgG class in six patients and IgA class in five. The molecular sizes of the protein antigens observed ranged from 58 to 120 kDa. 5. These results suggest that a proportion of patients with alcoholic heart muscle disease develop immunogenic cardiac protein—acetaldehyde adducts. The presence of antibodies to these adducts may be a marker for the diagnosis of this heart disease, or possibly for its pathogenesis.

1991 ◽  
Vol 81 (s25) ◽  
pp. 16P-16P
Author(s):  
A J Jacob ◽  
K M McLaren ◽  
N A Boon

1993 ◽  
Vol 85 (s29) ◽  
pp. 36P-36P
Author(s):  
A Harcombe ◽  
J Koskinas ◽  
G Kenna ◽  
Hjf Why ◽  
PJ Richardson ◽  
...  

1995 ◽  
Vol 25 (2) ◽  
pp. 386A
Author(s):  
Masakazu Teragaki ◽  
Masahiko Takagi ◽  
Tomoko Tani ◽  
Minoru Yoshiyama ◽  
Iku Toda ◽  
...  

Author(s):  
William J. McKenna ◽  
Perry Elliott

The term cardiomyopathy is used to describe heart muscle disease unexplained by abnormal loading conditions (hypertension, valve disease, etc.), congenital cardiac abnormalities, and ischaemic heart disease. The current classification is based on the predominant phenotype, i.e. hypertrophic, dilated, arrhythmogenic right ventricular, restrictive and unclassifiable (including left ventricular noncompaction), and—where possible—incorporating inheritance and genotype. Cardiomyopathies associated with systemic diseases are described in ...


2021 ◽  
Vol 15 (12) ◽  
pp. e0010017
Author(s):  
Lisa Hefele ◽  
Antony P. Black ◽  
Trinh Van Tan ◽  
Nguyen Tri Minh ◽  
Nguyen Duc Hoang ◽  
...  

The epidemiology of typhoid fever in Lao People`s Democratic Republic is poorly defined. Estimating the burden of typhoid fever in endemic countries is complex due to the cost and limitations of population-based surveillance; serological approaches may be a more cost-effective alternative. ELISAs were performed on 937 serum samples (317 children and 620 adults) from across Lao PDR to measure IgG antibody titers against Vi polysaccharide and the experimental protein antigens, CdtB and HlyE. We measured the significance of the differences between antibody titers in adults and children and fitted models to assess the relationship between age and antibody titers. The median IgG titres of both anti-HylE and CdtB were significantly higher in children compared to adults (anti-HylE; 351.7 ELISA Units (EU) vs 198.1 EU, respectively; p<0.0001 and anti-CdtB; 52.6 vs 12.9 EU; p<0.0001). Conversely, the median anti-Vi IgG titer was significantly higher in adults than children (11.3 vs 3.0 U/ml; p<0.0001). A non-linear trend line fitted to the anti-CdtB and anti-HlyE IgG data identified a peak in antibody concentration in children <5 years of age. We identified elevated titers of anti-HlyE and anti-CdtB IgG in the serum of children residing in Lao PDR in comparison to adults. These antigens are associated with seroconversion after typhoid fever and may be a superior measure of disease burden than anti-Vi IgG. This approach is scalable and may be developed to assess the burden of typhoid fever in countries where the disease may be endemic, and evidence is required for the introduction of typhoid vaccines.


1991 ◽  
Vol 68 (8) ◽  
pp. 805-807 ◽  
Author(s):  
Ashok J. Jacob ◽  
Kathryn M. McLaren ◽  
Nicholas A. Boon

2001 ◽  
Vol 25 (10) ◽  
pp. 1409-1413 ◽  
Author(s):  
Olli A. Kajander ◽  
Markku Kupari ◽  
Markus Perola ◽  
Jarkko Pajarinen ◽  
Vesa Savolainen ◽  
...  

2001 ◽  
Vol 25 (3) ◽  
pp. 457-463 ◽  
Author(s):  
Shann D. Kim ◽  
Jennifer Beck ◽  
Teresa Bieniarz ◽  
Autumn Schumacher ◽  
Mariann R. Piano

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