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SA JOURNAL OF DIABETES & VASCULAR DISEASE

RESEARCH ARTICLE

VOLUME 14 NUMBER 1 • JULY 2017

33

Association of homocysteinaemia with hyperglycaemia,

dyslipidaemia, hypertension and obesity

DUDU SENGWAYO, MPHO MORABA, SHIRLEY MOTAUNG

Correspondence to: Shirley Motaung

Dudu Sengwayo

Department of Biomedical Sciences, Faculty of Science, Tshwane University of

Technology, Pretoria, South Africa

e-mail:

motaungsckm@tut.ac.za

Mpho Moraba

Department of Medical Science, Health Public and Health Promotion,

School of Health Sciences, Faculty of Health Sciences, University of Limpopo

(Turfloop Campus), Sovenga, South Africa

Previously published in

Cardiovasc J Afr

2013;

24

: 265–269

S Afr J Diabetes Vasc Dis

2017;

14

: 33–37

Abstract

Aim:

Hyperhomocysteinaemia and the metabolic syndrome

are associated with increased cardiovascular risk. We

investigated whether there is a link between the metabolic

syndrome or its components and homocysteine levels in a

population without cardiovascular disease.

Methods:

From the population sample of 382 participants

(286 females and 96 males) we isolated those reflecting

the metabolic syndrome and determined their homo-

cysteine levels. We then evaluated the association of

homocysteine with hyperglycaemia, hypertriglyceridaemia,

hypercholesterolaemia, hypertension and obesity, using a

significance level of

p

= 0.05. Enzymatic methods were used

for all biochemical parameters.

Results:

We found the statistical relationship between

homocysteine and the metabolic syndrome as follows:

hyperglycaemia (

p

= 0.175), hypertriglyceridaemia (

p

=

0.442), hypercholesterolaemia (p = 0.480), obesity (

p

= 0.080);

and hypertension: systolic pressure (

p

= 0.002) and diastolic

pressure (

p

= 0.033).

Conclusion:

We found no statistically significant association

between baseline plasma homocysteine levels and the

metabolic syndrome, except for hypertension.

Keywords:

hyperglycaemia, hypertriglyceridaemia, hypercholes-

terolaemia, hypertension, obesity, homocysteine

Diabetes mellitus is a group of metabolic diseases characterised by

hyperglycaemia, resulting from defects in insulin secretion, insulin

action or both. It is associated with several cardiovascular disorders,

including angiopathy and platelet hyperactivity, which are major

causes of morbidity and mortality in type 2 diabetes mellitus.

1

Atherosclerosis is substantially more prevalent and progresses

rapidly in diabetes mellitus.

2

There are an estimated 23.6 million people in the USA (7.8%

of the population) with diabetes.

1

The vascular complication of

diabetes mellitus, at its earliest stage, is manifested as endothelial

dysfunction,

3

decreasing the bioavailability of nitric oxide, which

protects blood vessels from endogenous injuries.

4

Hyperglycaemia

inhibits fibrinolysis by decreasing the activity of plasminogen

activator and enhances coagulation by activating procoagulants

into thrombosis.

5

Homocysteine is an amino acid derived from methionine.

The latter is an intermediate in the conversion of homocysteine

to cysteine. Homocysteine is metabolised via two pathways:

remethylation, in which homocysteine is converted into methionine,

and transulphuration, in which homocysteine is converted into

cysteine. In the former pathway, homocysteine acquires a methyl

group, either from the conversion of 5-methyltetrahydrofolate

into hydrofolate or from the conversion of betaine into the N’

N-dimethylglycine.

6

Vitamins B

12

and B

6

are important in the

conversion of 5-methyltetrahydrofolate into hydrofolate and

therefore for the remethylation pathway and the metabolism of

homocysteine into methionine.

7

Epidemiological studies suggest hyperhomocysteinaemia to

be an independent risk factor for developing atherothrombotic

vascular disease.

8

Mechanisms by which hyperhomocysteinaemia

causes vascular disease include promotion of atherosclerosis by

damaging the inner lining of arteries and promoting thrombosis

through pathological collagen activation of the intrinsic pathway,

9

impairment of thrombolysis, increased production of hydrogen

peroxide, endothelial dysfunction, and increased oxidation of low-

density lipoproteins.

8

Some of the complications of arterial thrombosis following

hyperhomocysteinaemia include coronary heart disease, myocardial

infarction, stroke, peripheral vascular disease, miscarriage,

pulmonary embolism, retinal embolismand neural tube defect (spina

bifida).

9

The homocysteine level may be increased in hypertensive,

overweight and obese subjects.

10

Homocysteine is thought to help regulate glucose metabolism

and insulin absorption.

11

Homocysteine has been suggested to

contribute to the atherosclerotic process of diabetes mellitus. High

homocysteine levels have been reported in diabetic patients,

2,12

and elevated levels are a strong risk factor in these patients.

1

The

elevation occurs particularly in patients with type 2 diabetes, as

well as in individuals in prediabetic states who exhibit insulin

resistance.

13

The levels of homocysteine in such individuals are also

influenced by their insulin concentrations, and therapy with insulin

and medications such as metformin and glitazones that can either

raise or lower homocysteine levels.

12

The effect of hyperhomocysteinaemia on diabetes and

insulin resistance has been reported with unclear synergism.

12

Homocysteine levels have been reported as either low or elevated

compared to non-diabetic subjects, reflecting the potential role of

homocysteine in the development of macro- and microvascular

disease in diabetic patients.

13,1

Shaikh

et al

. found that 58% of their

diabetic participants had elevated homocysteine levels and males

were predominant in this group.

1

This finding is consistent with that

of Schalinske’s study.

14