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Only a limited number
of drugs are available to influence the levels of high density lipoprotein
cholesterol (HDL-C) in human beings. A low level of high density
lipoprotein cholesterol is now considered to be a risk factor for
coronary heart disease (CHD) . Fifty-one cases of hypercholesterolaemia
with increased ratios of total cholesterol to high density lipoprotein
cholesterol were selected for a clinical trial with an indigenous
remedy, Abana. After 12 weeks of therapy, high density lipoprotein
cholesterol levels showed an increasing trend. The ratio of total
cholesterol/high density lipoprotein cholesterol was modified after
therapy. This indicates that Abana can prevent coronary heart disease
in coronary-prone cases. Hence Abana may be advocated for cardioprotective
therapy.
An
inverse association between the incidence of CHD and HDL-C concentrations
has been observed. In multiple epidemiologic studies, different
ethnic groups have shown decreased HDL and elevated low density
lipoprotein (LDL) levels as a potent risk factor of CHD6-10.
Several factors are now known to alter the levels of HDL-C. Age,
sex, body-mass index, exercise and alcohol intake are associated
with HDL-C levels. Diet and drugs also alter the levels of HDL-C
in clinical as well as in experimental studies.
More
recently Gemfibrozil was found useful in increasing HDL-C. Continuous
use of this drug also reduces TC, LDL-C and triglycerides (TG)4.
In the Lipid Research Clinics Program Prevalence Study3
(LRPPS), a positive correlation was noted between dietary cholesterol
intake and serum cholesterol levels in schoolboys. Evidence from
animal studies has suggested that dietary protein influences plasma
protein levels. But in human beings, the findings are not consistent5.
In
the Ayurvedic system of medicine several drugs have been mentioned
as cardioprotective. Scientific evaluation of such drugs is, however,
limited. In recent years global attention has been directed towards
the clinical evaluation of indigenous drugs in the prevention and
management of CHD. Abana is a herbomineral compound generally advocated
for angina pectoris and coronary heart disease (CHD). It improves
the contractility of the heart and regulates lipoprotein metabolism
in CHD cases. Abana also exerts a significant influence on lipoprotein
levels1.
Abana
is a combination of Terminalia arjuna (Arjuna), Withania
somnifera (Ashwagandha), Phyllanthus emblica (Amla),
Glycyrrhiza glabra (Yashtimadhu), Boerhaavia diffusa
(Punarnava), Centella asiatica (Brahmi), Convolvulus pluricaulis
(Shankhapushpi), Nardostachys jatamansi (Jatamansi), Pearl
pishti (Moti), etc., in varying doses.
Fifty-one
diagnosed cases of hypercholesterolaemia were selected for this
clinical trial with Abana. Most of the cases had evidence of angina
pectoris, hypertension and obesity. Cases having evidence of diabetes
mellitus were excluded from this series. A comprehensive clinical
examination was carried out. Apart from routine investigations,
glucose tolerance and obesity index were also measured. For comparable
results, apparently normal individuals with no evidence of lipid
disorders were selected to serve as controls.
The
overnight fasting blood sample was taken and the serum TC12
and HDL-C8 were measured. After careful clinical and
laboratory examination, Abana was introduced at a dosage of 2 tablets
t.i.d. continuously for twelve weeks. The normal as well as hypercholesterolaemic
cases were advised a prescribed regimen of diet and exercise during
the entire course of study. At the end of twelve weeks all the investigations
were repeated. Those cases who could not follow the prescribed regimen
diet and therapy were excluded from the series. The initial findings
were compared with those after 12 weeks of follow-up.
A significant
elevated level of TC was noticed in the present series, the ratio
of TC/HDL-C being found increased (>3.5) (Table 1). After 3 months
of therapy a reverse trend was observed. TC showed a decreasing
trend and the ratio also decreased to a significant extent. In the
normal control series no significant changes in either the TC and
HDL-C levels were observed (Table 2). Thus it is evident that Abana
has a capacity to modify the increased TC/HDL-C ratio.
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Table 1: Effect
of Abana therapy on total cholesterol and HDL cholesterol
(mean ± S.D.)
|
|
Group
|
Total
cholesterol
(mg/dl)
n = 51
|
HDL
cholesterol
(mg/dl)
n=51
|
TC/HDL-C
(risk factor)
|
| Initial |
280.09
± 46.68
|
49.05
± 11.72
|
6.19
± 2.30
|
| After
12 weeks of therapy |
204.08
± 40.66
|
54.07
± 11.89
|
4.03
± 1.43
|
Comparison:
Initials vs. after 12 weeks of therapy |
p<0.001
|
p<0.05
|
p<0.001
|
|
Table 2: Pattern
of total cholesterol and HDL cholesterol in the control group
|
|
Group
|
Total
cholesterol
(mg/dl)
n = 10
|
HDL
cholesterol
(mg/dl)
n=10
|
TC/HDL-C
(risk factor)
|
| Initial |
255.100
± 16.842
|
51.60
± 6.433
|
4.962
± 0.779
|
| After
12 weeks of therapy |
268.800
± 20.302
|
49.80
± 5.266
|
5.397
± 0.722
|
Comparison:
Initials vs. after 12 weeks of therapy |
p<0.05
N.S.
|
p<0.05
N.S.
|
p<0.05
N.S.
|
| N.S.
= Not significant |
As
indicated earlier, HLD-C is one of the most important risk factors
for the development of CHD. High HDL-C prevents atherosclerosis
and reduces the risk of CHD. Alcohol and moderate exercise are responsible
for increasing the level of HDL-C7,9. The hypolipidaemic
drugs generally do not elevate HDL-C. That drug which can increase
the level of HDL-C may be considered as a cardioprotective. Abana
contains: T. arjuna which is a known cardioprotective component.
The hypocholesterolaemic property of T. arjuna has also been
reported by some investigators11. But it is not known
for certain, which component of Abana enhances the HDL level. It
is possible that the combined effect of several ingredients may
be responsible for the significant increase. Earlier it has been
reported that Abana reduces the cholesterol and triglyceride levels
in CHD patients2. The increasing trend of HDL-C levels
has provided us with a ground for more precise investigation to
evaluate the effect of Abana on the TC/HDL-C ratio. From Table 1
it is evident that the TC/HDL-C ratio dropped significantly after
12 weeks of Abana therapy. It indicates that this drug has a cardioprotective
property. The continuous oral administration of Abana may prevent
the development of CHD.
The
present study is preliminary in nature and requires a bigger sample
size to prove the beneficial effect of Abana.
-
Agarwal, U., Dubey, M.L. and Dubey, G.P. Coronary
risk factors and their management by an indigenous drug Abana.
Probe 2 (1988), 120.
-
Dubey, G.P., Agarwal, A., Srivastava, V.K.
and Udupa, K.N. Management of risk factors of CHD with an indigenous
compound Abana (A controlled study). Probe 1 (1985),
46.
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Ernst, N., Fisher, N., Smith, W., et al.
The association of high density lipoprotein cholesterol with
dietary intake and alcohol consumption. The Lipid Research Clinics
Program Prevalence Study. Circulation 62 Suppl. 41 (1980),
41.
-
Frick, M.H., Elo, O., Happa, J., Heinomen,
O.P., et al. Helsinki Heart Study: Primary prevention
trial with Gemfibrozil in middle aged men with dyslipidaemia.
N. Engl. J. Med. 317 (1987), 1237.
-
Glueck, C.J., Waldman, G., McClish, D.K., et
al. Relationship of nutrient intake to lipids and lipoproteins
in 1234 white children. Arteriosclerosis 2 (1982), 523.
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Goldbourt, U., Holtzman, E. and Neufeld, H.N.
total and high density lipoprotein cholesterol in the serum
and risk of mortality: evidence of a threshold effect. Br.
Med. J. 290 (1985), 1239.
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Gordon, T., Ernst, N., Fisher, M. and Rifkind,
B.M. Alcohol and high density lipoprotein cholesterol. Circulation
64 Suppl. 3 (1981), 63.
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Lopez-Virella, M.F., Stone, P., Ellis, S. and
Colwell, J.A. Clin. Chem. 23 (1977), 882.
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Masarie, J.R.L., Puddey, I.B., Rouse, I.L.,
Lynch, W.J., Candengen, R. and Bellin, J.L. Effect of alcohol
consumption on serum lipoprotein lipid and apolipoprotein concentrations.
Atherosclerosis 60 (1986), 79.
-
Pocock, S.J., Shaper, A.G., Phillips, A.N.,
Walker, M. and Whitehead, T.P. High density lipoprotein cholesterol
is not a major risk factor for ischaemic heart disease in British
men. Br. Med. J. 292 (1986), 515.
-
Udupa, K.N. Scope of use of Terminalia arjuna
in ischaemic heart disease. Ann. Natl. Acad. Ind. Med.
I (1986). BHU.
-
Zurkowski, P.A. rapid method for cholesterol
determination with a single reagent. Clin. Chem. 10 (1964),
451.
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