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1.
S. K. Sen P. Pukazhvanthen Rebecca Abraham 《Indian journal of clinical biochemistry : IJCB》2008,23(3):255-257
Elevated plasma Homocysteine level is an independent risk factor for age related (senile) cataract. Certain nutritional deficiencies,
in particular Folate, Vitamin B12, Vitamin B6 relate inversely with Homocysteine level. This study was undertaken to evaluate the plasma level of Vitamin B12, Folate, and Homocysteine of cataract patients and to study the interplay between them. Serum Homocysteine level is significantly
increased in cataract patients when compared with control (p< 0.001). There was a significant decrease in the level of Folate
as compared with control (p<0.001). There was a negative correlation between Homocysteine vs. Vitamin B12 (p<0.01) and Folate (p<0.01) in the Cataract patients. Our findings suggest that increased plasma Homocysteine level is associated
with decreased plasma levels of Folate and VitaminB12 in Cataract patients, which might have a possible role in the root cause of cataract pathogenesis. 相似文献
2.
M. N. Sadananda Adiga Sunil Chandy Girija Ramaswamy L. Appaji B. S. Aruna Kumari Lakshmi Krishnamoorthy 《Indian journal of clinical biochemistry : IJCB》2009,24(3):257-261
Remethylation of homocysteine to methionine is dependent on an adequate supply of one or more of the B vitamins like folate,
vitamin B12 and vitamin B6. Plasma total homocysteine (tHcy) is also influenced by genetic factors such as polymorphisms in the methylenetetrahydrofolate
reductase (MTHFR) gene. MTHFR is a flavo enzyme and a key player in folate metabolism and changes in its activity could modify
the susceptibility to Acute Lymphoblastic Leukemia (ALL). In this case — control study we have examined the effect of riboflavin
status as measured by erythrocyte glutathione reductase activation coefficient (EGRAC) on homocysteine levels along with vitamin
B12 and folate in pediatric ALL. Folate and B12 levels were significantly lower among cases as compared to controls while EGRAC and tHcy did not differ significantly among
the groups. The multivariate regression analysis revealed that in the ALL group EGRAC significantly influences tHcy levels
suggesting that riboflavin availability may be a predictor of tHcy levels in patients with ALL. This finding may have implications
for tHcy lowering therapy. 相似文献
3.
Vitamin B12 being water soluble is excreted in the urine when administered in excess. The probability of finding an abnormally excess
serum concentration would be almost surreal. We report a peculiar clinical situation that may impact the vitamin B12 immunoassay on the Roche Elecsys 2010 due to excess analyte concentration. In separate episodes (Feb and June 2010), the
Biochemistry laboratory of a tertiary-care hospital, Kolkata, India, encountered two critically ill patients with background
chronic kidney disease (CKD), low urine output, and on cyanocoabalamin supplementation, who had serum vitamin B12 concentrations far exceeding expected values; even post dialysis. The B12 assays (pmol/l) were performed using electrochemiluminiscence immunoassay on Roche Elecsys 2010, the assay validity confirmed
by concomitant quality control runs. The immunoassays failed to deliver results, flagged with “signal level below limit”. Biotin therapy was ruled out as a possible interferent. In the first episode, re-assay of a repeat draw yielded same outcome;
outsourcing on Immulite provided concentration of >738 pmol/l. Serial dilution gave result of >29520 pmol/l on Elecsys 2010.
In the second, we gained from past experience. Vitamin B12 concentration >59040 pmol/l was conveyed to the treating nephrologist the very day. The B12 immunoassay on the Elecsys 2010 employs sequential incubation steps for competitive binding that is compromised in the event
of abnormally excess B12 concentration in patient sera akin to the prozone effect. This knowledge may be beneficial while assaying sera of CKD patients
to avoid financial loss due unnecessary repeats and delay in turnaround time. 相似文献
4.
Itemobong S. Ekaidem Monday I. Akpanabiatu Friday E. Uboh Offiong U. Eka 《Indian journal of clinical biochemistry : IJCB》2007,22(2):36-40
Folic acid and vitamin B12 are very important vitamins needed for normal cellular metabolic activities. The effects of folic acid and vitamin B12 on liver integrity of growing Wistar albino rats following therapeutic dose of phenytoin administration were investigated.
The activities of serum AST, ALT, ALP were investigated. Serum total protein level and lipid profile were also measured as
indices of biochemical changes. The ingestion of phenytoin alone in rats significantly reduced serum protein while AST, ALT
activities incresed as compared to the control (P<0.05). Supplementation of phenytoin with oral administration of 70microgram/kg
body wt of folic acid resulted in a significant reversal in serum total protein and suppression in serum AST and ALT activities.
Vitamin B12 supplementation did not afford any significant protection against the effect of phenytoin ingestion but rather phenytoin
toxicity was exacerbated in this study. However, the combined effects of vitamin B12 and folic acid ameliorated the effects of phenytoin on serum enzymes of experimental rats. The effect of combination of phenytoin
with folic acid or folic acid and vitamin B12 is an interesting finding. Supplementation of phenytoin with folic acid or combination of these vitamins may be recommended
for the purpose of ameliorating the adverse biochemical changes which are associated with phenytoin therapy. Further work
is ongoing to help elucidate the effects of phenytoin and these vitamins on oxidative stress inducing mechanism. 相似文献
5.
A. S. Yadav V. R. Bhagwat I. M. Rathod 《Indian journal of clinical biochemistry : IJCB》2006,21(1):106-110
The present study was undertaken to explore the relationship of plasma homocysteine with other biochemical parameters in ischemic
heart disease. Plasma levels of total homocysteine was measured by HPLC—fluorescence detection with internal standard in 60
ischemic heart disease patients and were compared with 30 age matched normal healthy controls. The significant increase of
plasma homocysteine was observed in both myocardial infarction and chronic stable ischemic heart disease patients when compared
with the controls. The hyperhomocysteinemia appears be to due to increased body demand of vitamins such as folic acid, vitamin
B12, B6, B2 either alone or in combination to regulate normal homocysteine metabolism. 相似文献
6.
R Abraham M Joseph John R Calton J Dhanoa 《Indian journal of clinical biochemistry : IJCB》2006,21(1):95-100
Homocysteine(Hcy) has been implicated as a novel risk factor of Coronary Artery Disease (CAD) among Asian Indians, but many
studies done in India failed to reveal any direct correlation. It has also been reported that Folic acid and Vitamin B12 levels
inversely affect serum levels of homocysteine. In this study, we looked at the levels of homocysteine among patients with
CAD. The effect of Vitamin B12, Folate and other risk factors on homocysteine levels were also evaluated. Mean homocysteine
levels in cases (22.81±13.9, n=70) were significantly higher (p=<0.001) than the controls (7.77±7.3, n=70). However no statistically
significant correlation could be deduced between homocysteine Vitamin B12, and Folate. Cumulative analysis have indicated
an increase in homocysteine levels among patients with CAD with every additional risk factor. 相似文献
7.
S. Vasisht R. Gulati R. Narang N. Srivastava L. M. Srivastava S. C. Manchanda D. P. Agarwal 《Indian journal of clinical biochemistry : IJCB》2002,17(1):99-107
An elevated level of plasma homocysteine, sulfur containing amino acid generated through demethylation of methionine has been
widely accepted as a risk factor for cardiovascular disease (CVD). The increase can result from genetic and/or nutrient related
disturbances in the remethylation or transsulfuration pathways for homocysteine metabolism. A common mutation (C677T) in the
gene encoding for the enzyme 5, 10-methylenetetrahydrofolate reductase (MTHFR) or deficiency of the B vitamins namely folic
acid, B12, B6 can lead to hyperhomocysteinemia.
In the present study, we have investigated the incidence of the (C677T) MTHFR polymorphism in the North Indian males. 141
angiographically proven coronary artery disease (CAD) patients and 55 age and sex matched healthy volunteers were examined
for the association between MTHFR gene polymorphism and CAD. The MTHFR genotyping was performed using polymerase chain reaction
(PCR) followed by restriction-isotyping with Hinf 1 endonuclease. A trend for higher ‘T’ allele frequency (0.19) was observed
in patients than in controls (0.16). However no significant association was found between C677T mutation and CAD severity.
The lack of statistical significance could be due to the small sample size studied. Hence a larger study including various
ethnic groups is warranted. 相似文献
8.
Seema Bhargava R. Parakh L. M. Srivastava 《Indian journal of clinical biochemistry : IJCB》2004,19(1):76-78
Homocysteine (Hcy) is a non-protein forming amino-acid, whose metabolism is at the intersection of two metabolic pathways:
remethylation and transsulfuration which are dependent on the vitamins folic acid, B12 and B6, and the enzymes methylenetetrahydrofolate reductase and cystathionine-β-synthetase. A deficiency of any of these vitamins
or enzymes results in hyperhomocysteinemia. This causes oxidative and other damage to blood vessels, thus affecting various
organ systems of the body. As part of our ongoing research on cardiovascular risk factors, we have studied the Hcy levels
in the plasma of normal controls and those suffering from vascular diseases. It was observed that Hcy is significantly higher
in patients of vascular diseases (21.59±1.28 μmol/L, mean±SEM), as compared to normal controls (11.33±0.18 μmol/L). This significance,
was more pronounced in cases of venous thrombosis (26.77±2.43 μmol/L) as opposed to cases of arterial block (17.27±0.84 μmol/L).
This signifies that Hcy estimation would be beneficial in obtaining a differential diagnosis in addition to being a modifiable
vascular risk factor. 相似文献
9.
G. Sharmila Banu Ganeshan Kumar A. G. Murugesan 《Indian journal of clinical biochemistry : IJCB》2009,24(3):250-256
Aflatoxins are potent hepatotoxic and hepatocarcinogenic agents. Reactive oxygen species and consequent peroxidative damage
caused by aflatoxin are considered to be the main mechanisms leading to hepatotoxicity. The present investigation aims at
assessing the hepatoprotective effect of ethanolic leaves extract of Trianthema portulacastrum on aflatoxin B1 (AFB1)-induced hepatotoxicity in a rat model. The hepatoprotection of T. portulacastrum is compared with silymarin, a well known
standard hepatoprotectant. Lactate dehydrogenase, alkaline phosphatase, alanine and aspartate aminotransferases were found
to be significantly increased in the serum and decreased in the liver of AFB1 administered (1 mg/kg bw, orally) rats, suggesting hepatic damage. Marked increase in the lipid peroxide levels and a concomitant
decrease in the enzymic (superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase, glucose-6-phosphate
dehydrogenase and glutathione-S-transferase) and nonenzymic (reduced glutathione, vitamin C and vitamin E) antioxidants in
the hepatic tissue were observed in AFB1 administered rats. Pretreatment with T. portulacastrum (100 mg/kg/p.o) and silymarin
(100 mg/kg /p.o) for 7 days reverted the condition to near normal. The results of this study indicate that the ethanolic leaves
extract of T. portulacastrum is a potent hepatoprotectant as silymarin. 相似文献
10.
Chemoprevention represents a new intervention strategy to control some type of carcinogenesis especially in subjects at high
risk for cancer development. Experimental and epidemiological data indicate that a variety of nutritional factors including
vitamin C and E are effective to lower the risk of some types of cancer. However large prospective studies have failed to
find such significant association. A comparative and combined in vitro antimutagenic potential of two antioxidant vitamins
ascorbic acid (vitamin C) and α-tocopherol (vitamin E) were evaluated using Ame’s Salmonella typhimurium test assay. Directly
acting mutagens such as sodium azide (NaN3) and 4-Nitro-o-phenylenediamine (NPDA), and N-methyl-N′-nitro-N-nitrosoguanidine (MNNG) were used to induce mutation in salmonella strains
TA 98 and TA 100. Vitamin C significantly (P < 0.01) and dose dependently inhibited the mutagenicity induced by all the three mutagens. The percent inhibitions of vitamin
C at 15 mg/plate were 33.8% (NaN3), 52.5 % (MNNG) and 55.4 % (NPDA). Vitamin E (15 mg/plate) was effective to inhibit mutagenicity induced by NaN3 and MNNG
but did not inhibit mutation induced by NPDA. Combination of vitamins (vitamin C plus vitamin E) produced only an additive
antimutagenic activity when compared to their activity at 5 mg/plate. The results of the study concluded that vitamin C is
a better antimutagenic agent than vitamin E and combination of vitamins did not produce any synergistic activity. 相似文献
11.
C. R. Wilma Delphine Silvia D. M. Vasudevan K. Sudhakar Prabhu 《Indian journal of clinical biochemistry : IJCB》2002,17(2):104-107
Serum β2-microglubin (β2-m) levels were measured in oral carcinoma patients and compared with normal healthy controls. It was observed that there
was a significant rise in serum β2-microglobulin in oral carcinoma patients. Progressively higher values were obtained as the cancer advanced clinically. Therefore
the estimation of serum β2-microglobulin may be useful as one of a battery of tests in the assessment of oral carcinoma patients. 相似文献
12.
A. P. S. Narang S. Batra S. Sabharwal S. C. Ahuja 《Indian journal of clinical biochemistry : IJCB》2004,19(2):111-113
In the present study primary involution osteoporosis and vitamin D levels were studied in 60 subjects including thirty controls.
The biochemical analysis of serum calcium, phosphorus, ALP, albumin and vitamin D3 (1,25-(OH)2 D3) levels were significantly decreased in osteoporotic patients when compared to non-osteoporotic control group. There was
a significant correlation of magnitude of sun exposure with 1,25-(OH)2 D3 levels. Similarly, vitamin D intake in the diet has a significant correlation with 1,25-(OH)2 D3 concentration. However, no correlation could be obtained between vitamin D3 levels with increasing age. Among the biochemical markers serum calcium, phosphorus, ALP and albumin could not be correlated
with 1,25-(OH)2 D3 levels. 相似文献
13.
V. K. Gupta V. Mallika Yashika Gupta D. K. Srivastava 《Indian journal of clinical biochemistry : IJCB》1992,7(1):3-10
Oxygen derived free radicals have been implicated in a number of clinical disorders including atherosclerosis (1), ischemic
heart disease (IHD) (2), post ischemic reperfusion injury (3) and respiratory distress syndrome (4). These radical are generated
by sequential reduction of molecular oxygen; the primary product being superoxide anion (O2
.−) which is subsequently reduced to hydrogen peroxide (H2O2), hydroxy1 radical (OH.) and singlet oxygen (1O2). However the evidence for ODFR induced cell damage in various clinical disorders is still debated and rests largely on free
radical scavenging studies, through electron paramagnetic resonance spectroscopic (EPRS) studies have provided direct evidence
for ODFR generation following coronary artery ligation (5).
By definition, a free radical is an atom, ion or molecule with one or more unpaired electrons (the presence of unpaired electron
in a free radical being represented by a superscribed bold dot-R.) and may be formed as a result of homolytic fission of a covalent bond or by electron transfer reactions, and may have cationic
(NH3
+), anionic (O2
.−) or neutral (NO) characteristics. The most important in vivo source for these radical species have been found to be univalent
biochemical redox reactions involving oxygen. (a) A:B→A.+B. (b) A:+B→A.+B. 相似文献
14.
Cataract is one of the leading causes of visual disability often leading to blindness in the elderly population. One of the
causes is oxidation of proteins present in lens, by hydrogen peroxide (H2O2). In the present study 100 goat lenses were analyzed to determine the protective efficacy of ketoacids, against the oxidative
insult by H2O2. The ketoacids used were (pyruvate, alpha ketoglutarate and oxaloacetate), that are constantly produced endogenously. The
lenses were incubated as control and experimental groups in TC-199 media for 72 hrs. H2O2 concentration of 10mM was used to induce cataract. The biochemical parameters measured were levels of malondialdehyde (MDA),
a lipid peroxidation product and activity of glutathione peroxidase (G-Px), an enzymatic antioxidant. The results showed a
significant increase in the levels of MDA and significant decrease in the activity of G-Px in the cataractous lenses as compared
to control. After addition of ketoacids (pyruvate (10mM), alpha ketoglutarate (20mM) and oxaloacetate (20mM)) separately,
the levels of MDA decreased significantly and the activity of G-Px increased significantly. The results suggest that the ketoacids
can be very promising antioxidants for the treatment of cataract. They may also be useful in treating other disabilities related
to acute and chronic oxidative stress. 相似文献
15.
Samanta L Panigrahi J Bhanja S Chainy GB 《Indian journal of clinical biochemistry : IJCB》2010,25(4):393-397
The present study was designed to compare the potential of turmeric and its active principle curcumin on T3-induced oxidative stress and hyperplasia. Adult male Wistar strain rats were rendered hyperthyroid by T3 treatment (10 μg · 100 g−1 · day−1 intraperitoneal for 15 days in 0.1 mM NaOH) to induce renal hyperplasia. Another two groups were treated similarly with T3 along with either turmeric or curcumin (30 mg kg−1 body weight day−1 orally for 15 days). The results indicate that T3 induces both hypertrophy and hyperplasia in rat kidney as evidenced by increase in cell number per unit area, increased protein
content, tubular dilation and interstitial edema. These changes were accompanied by increased mitochondrial lipid peroxidation
and superoxide dismutase activity without any change in catalase activity and glutathione content suggesting an oxidative
predominance. Both turmeric and curcumin were able to restore the level of mitochondrial lipid peroxidation and superoxide
dismutase activity in the present dose schedule. T3-induced histo-pathological changes were restored with turmeric treatment whereas curcumin administration caused hypoplasia.
This may be due to lower concentration of curcumin in the whole turmeric. Thus it is hypothesized that regulation of cell
cycle in rat kidney by T3 is via reactive oxygen species and curcumin reveres the changes by scavenging them. Although the response trends are comparable
for both turmeric and curcumin, the magnitude of alteration is more in the later. Turmeric in the current dose schedule is
a safer bet than curcumin in normalizing the T3-induced hyperplasia may be due to the lower concentration of the active principle in the whole spice. 相似文献
16.
R. Dhananjayan T. Malati Y. Rupasree Vijay Kumar Kutala 《Indian journal of clinical biochemistry : IJCB》2015,30(3):263-270
The present work was aimed to study the association of one carbon genetic variants, hyperhomocysteinemia and oxidative stress markers, i.e., serum nitrite, plasma malondialdehyde (MDA) and glutathione (GSH) on intimal medial thickening (IMT) in patients with type 2 diabetes mellitus (T2D). A total number of 76 subjects from ACS Medical College and Hospital, Chennai, India were included in the study, i.e., Group I (n = 42) of T2D and Group II (n = 34) of age- and sex matched healthy controls. The glycated haemoglobin was measured by ion-exchange resin method; plasma homocysteine by Enzyme Linked Immunosorbant Assay method; serum nitrite (nitric oxide, NO), plasma MDA and GSH by spectrophotometric methods; the IMT by high frequency ultrasound. The polymorphisms of one carbon genetic variants were genotyped using polymerase chain reaction-restriction fragment length polymorphism and amplified fragment length polymorphism methods. Results indicate that methyltetrahydrofolate homocysteine methyl transferase (MTR) A2756G allele was found to be protective in T2D and the other variants were not significantly associated with T2D. Glutamate carboxypeptidase II (GCP II) C1561T (r = 0.34; p = 0.05) and methylene tetrahydrofolate reductase (MTHFR) C677T (r = 0.35; 0.04) showed positive correlation with plasma homocysteine in T2D cases. In this study, MTR A2756G allele was found to be protective in T2D; GCP II C1561T and MTHFR C677T showed positive association with plasma homocysteine in T2D cases. Among all the genetic variants, MTR A2756G was found influence IMT. RFC 1 G80A and TYMS 5′-UTR 2R3R showed synergistically interact with MTR A2756G in influencing increase in IMT. 相似文献
17.
Rajes Qvist Ikram Shah Ismail Karuthan Chinna Sekaran Muniandy 《Indian journal of clinical biochemistry : IJCB》2008,23(3):246-249
Although HbA1C is widely accepted as a useful index of mean blood glucose in type 2 diabetic patients its usefulness as screening test for
diabetes has been controversial. The present study was undertaken to determine whether the level of HbA1C predicted diabetes in a prediabetic group of subjects. Plasma lipids, oral glucose tolerance, HbA1C was determined in 90 normal control subjects, 57 offspring of one type 2 diabetes mellitus parent and 11 diagnosed type 2
diabetes mellitus individuals. The mean age of participants was 44.5 yrs (not significantly different amongst the three groups)
and the mean body mass index was 26.8 (not significantly different amongst the three groups). Two hours after a 75 g glucose
challenge, the offspring had a significantly higher plasma glucose level (mean = 7.1 mmol/L, p value = 0.002) than the normals. Similarly the HbA1C values were higher in the offspring than in the normals (mean = 5.78%, p value = 0.016). Besides the significantly higher values for oral glucose tolerance test and HbA1C, the diabetics also were significantly higher for triglycerides (mean = 2.25mmol/L), total cholesterol (mean = 6.24mmol/L)
and systolic blood pressure (mean = 138.45mm Hg) than the offspring (P value = 0.031, 0.006, 0.010) and the normals (P value = 0.026, 0.018, 0.002) respectively. The mean values of diastolic blood pressure, LDL cholesterol and HDL cholesterol
were not significantly different amongst the three groups. 相似文献
18.
Hanaa H. Elsaid Khaled A. El-Hefnawy Saffaa M. Elalawi 《Indian journal of clinical biochemistry : IJCB》2021,36(2):213
Homocysteine concentration affected by the activities of the enzymes methylene tetra-hyrdofolate reductase (MTHFR). Polymorphisms in MTHFR gene associated with an impairment of MTHFR activity. Hyperhomocysteinemia is a result of single nucleotide polymorphisms (SNPs) in MTHFR 677 C>T that can cause homocysteine levels in the blood to increase. The purpose of this study is to investigate the relationships between MTHFR C677T (rs1801133) gene polymorphism, changes in homocysteine concentrations and progress of renal impairment in young adult hypertensive patients. Two hundred young hypertensive patients (age 21–24 years) were involved in this study; they were classified into patients with and without renal impairment in addition to 200 age and sex matched healthy controls. All participants were submitted to laboratory investigations as assay of MTHFR gene polymorphism C677T (rs1801133) by PCR/RFLP, determination of lipid profile, homocysteine and folic acid concentrations in addition to urinary albumin creatinine ratio (UACR). The levels of both homocysteine and UACR in the TT genotype patients were higher than those in the CC genotype group. Individuals who carry the T allele were more risky to hypertension and progress to early renal impairment in young age compared with those carrying the C allele [OR 2.02 (1.33–3.08), P < 0.001]. Genetic variants of C677T MTHFR gene and hyperhomocysteinemia may be responsible for rapid progress of renal impairment in Egyptian young age hypertensive patients. TT genotype or T allele may be considered as a predisposing factor for both elevated Hcy levels and the development of renal impairment. This study believed that lowering of homocysteine level can reduce renal impairment of hypertensive patients. 相似文献
19.
There is ample evidence that vitamin status of an individual can have a profound influence on the resistance of Cancer. Pyridoxine
is one of the water soluble vitamins playing an important role in various metabolic reactions. Aspartate aminotransferase
and Alanine aminotransferase are pyridoxal phosphate requiring enzymes and their activities in erythrocytes have been used
to assess the state of vitamin B6 nutrition in man.
We report here the erythrocyte transaminase levels in controls and patients with early and advanced cancer of breast. Thein vitro study of vitamin B6 shows a marked difference in the per cent stimulation in patients as compared to the controls on addition of pyridoxal phosphate.
The difference indicates a subclinical deficiency of vitamin B6. The possibility exists that the rapid progression of the disease could be due to lack of host resistance caused by the deficiency
of vitamin B6. The possibility of an effective treatment response after enhancing the vitamin B6 status is being looked into. 相似文献
20.
V. Govindaraju Neelam C. N. Manjunath H. Venkataramiah T. R. Raghu 《Indian journal of clinical biochemistry : IJCB》2003,18(1):8-14
Conclusion There is considerable epidemiological evidence, which confirms the importance of plasma homocysteine as a powerful predictor
of future risk of coronary heart disease and other complications of atherosclerosis. Treatment of hyperhomocysteinemia varies
with the underlying cause. However, an inexpensive vitamin supplementation with folic acid, vitamin B12 and vitamin B 6 is
generally effective in reducing homocysteine concentrations. Several randomised, controlled trials evaluating the effects
of folic acid based supplements on homocysteine concentrations have been conducted over the last decade. In most patients,
folic acid alone, and in combination of vitamin B12 and B6, has been shown to reduce homocysteine concentrations within four
to six weeks after the initiation of therapy (34).
However, no study has yet demonstrated that lowering of homocysteine by vitamin supplementation decreases the cardiovascular
morbidity or mortality. Avoidance of excessive meat intake and increased consumption of fresh vegetables and fruits is a dietary
measure, which has many health benefits, including a potential to reduce elevated homocysteine levels. The other reasonable
approach is to determine levels of fasting homocysteine in high risk patients and it may be advisable to increase their intake
of vitamin fortified foods and/or to suggest the daily use of supplemental vitamins. Several large scale randomised trials
like Heart Outcomes Prevention Evaluation (HOPE-2) Study, Mcmaster University, Canada, Study of the Effectiveness of Additional
Reductions in Cholesterol and Homocysteine (SERCH), Clinical Trial Service Unit, Oxford, U.K, Cambridge Heart Antioxidant
Study (CHAOS-2) University of Cambridge, U.K, Bergen Vitamin Study, University of Bergen Norway, Women's Antioxidant and Cardiovascular
Disease Study (WACS) Harvard Medical School, U.S.A, Prevention with a combined inhibitor and folate in Coronary Heart Disease
(PACIFIC) study, University of Sydney, Australia, and many others are ongoing to assess the effect of homocysteine—lowering
by vitamin supplementation on risk of vascular disease. 相似文献