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. 2020 Apr 22;12(4):e7785. doi: 10.7759/cureus.7785

Correlation of Homocysteine Level and Age in Patients with Ischemic Stroke

Muhammad Omer Sultan 1, Umar Farooque 2,, Rafay Javed 3, Muhammad I Khan 1, Sundas Karimi 4, Rukhsana Abdul Sattar 5, Omer Cheema 6
Editors: Alexander Muacevic, John R Adler
PMCID: PMC7243624  PMID: 32461857

Abstract

Introduction

Hyperhomocysteinemia is associated with atherosclerosis, as it can be seen in inborn errors of methionine metabolism. Likewise, many studies have also reported more modest increases in serum homocysteine levels in other atherosclerotic disorders like cardiovascular disease and all types of stroke with a positive correlation with age. But overall literature is controversial. Therefore, this study is being conducted to further investigate the relationship between homocysteine ​​levels and age in patients, especially those with ischemic stroke.

Material and methods

This cross-sectional study is conducted at a major hospital in Karachi in which all patients with ischemic stroke, diagnosed within 24 hours on CT, and age 40-75 years of both genders were enrolled for six months. Other demographics were also noted like gender, smoking status, and comorbidities (diabetes mellitus [DM], hypertension [HTN]). The homocysteine level was also checked by collecting non-fasting blood. Vitamin B12 level was not checked. The age, weight, height, body mass index (BMI), and homocysteine level’s means and standard deviations and the gender, DM, hypertension, and smoking status frequencies and percentages were calculated. The correlation coefficient of homocysteine level and age was also calculated. Stratification was done to see the effects of gender, BMI, DM, and HTN on homocysteine levels by applying the chi-square test.

Results

The mean age of the patients was 55.60 ± 11.45 years. Gender distribution showed that 111 (62.40%) patients were male, and 67 (37.60%) patients were female. Diabetic, hypertensive, and smoking status of the patients was 58 (32.60%), 96 (53.90%), and 53 (29.80%), respectively. The mean homocysteine level was 14.61, with a standard deviation of 1.47. Pearson’s correlation test showed that there is no statistically significant correlation between homocysteine levels and age. But a significant linear relationship was found of homocysteine levels with DM and HTN. 

Conclusion

Further investigation of the relationship of homocysteine ​​levels with age, diabetes mellitus, and hypertension, and the role of homocysteine as a risk factor for ischemic stroke should be carried out on a larger scale to prove its accuracy. The benefits of screening for homocysteine ​​levels also need to be studied in the elderly, especially those with diabetes mellitus and hypertension, which can lead to timely prevention of strokes and ischemic heart disease with vitamin B supplements, and other appropriate interventions.

Keywords: homocysteine level, correlation, ischemic stroke, age, humans, diabetes mellitus, hypertension

Introduction

Homocysteine is a prothrombotic factor that affects coagulation and fibrinolytic cascades [1]. It also causes endothelial injury through direct toxicity and apoptosis which results in endothelial dysfunction causing impaired endothelium-dependent dilatation of blood vessels combined with a proinflammatory and proatherosclerotic endothelial phenotype [2, 3].

That’s why inborn errors of methionine metabolism, associated with very high levels of homocysteine, cause atherosclerosis [4]. But atherosclerotic diseases like coronary artery disease and stroke, without underlying hereditary disorders, can also have slightly increased serum homocysteine levels. In fact, some meta-analyses have shown independent stratified associations of homocysteine levels with stroke and ischemic heart disease [5, 6].

Stroke is a heterogeneous disease and different stroke subtypes have different pathophysiological mechanisms. Homocysteine ​​has been studied in stroke subtypes in various Asian and European populations, and most studies show that all stroke subtypes have high homocysteine ​​levels compared to controls [7-13]. Homocysteine levels were elevated in stroke patients (14.3±8.8 µmol/L) compared to controls (11.8±5.7 µmol/L). Homocysteine concentrations were separately elevated in both ischemic (14.3±8.9 µmol/ L) and hemorrhagic (14.5±8.7 µmol/L) strokes compared to controls. Furthermore, homocysteine was positively correlated with age in both ischemic and hemorrhagic strokes (r=0.211) and it was also associated with premature ischemic stroke in young patients [14, 15].

On robust search, we found that no local data on the correlation of homocysteine level and age in patients with ischemic stroke is available and there is scarce literature available internationally. Also, the data review showed that there is a lot of controversy about the importance of homocysteine ​​as a risk factor for CVD and stroke [16]. Therefore, the present study is designed with the view to generate local data and to estimate the strength of association of homocysteine level and age in patients with ischemic stroke.

Materials and methods

Study design and sampling

The cross-sectional study took place at Jinnah Postgraduate Medical Center, Karachi, from 6/7/2013 to 12/7/2013 (during six months). Non-probability consecutive sampling technique was applied. The sample size was calculated, taking into account that the null hypothesis with 5% type I and 10% type II errors, homocysteine level, and age correlation (r)15 =0.211, the sample size came out to be 178 patients with ischemic stroke. Inclusion criteria are age 40-75 years, either gender, patients with ischemic stroke diagnosed within 24 hours on CT. Exclusion criteria included patients with hemorrhagic stroke, recurrent ischemic strokes, subcortical infarction >15 mm diameter, cortical infarction, carotid, vertebral, or intracranial artery stenosis >50% on CT, and potential cardiac source of embolism.

Data collection

Ischemic stroke patients, diagnosed as specified in the operational definition meeting the inclusion criteria, admitted through the emergency department, were enrolled in the study. Prior to enrolment, the pros and cons of the study were explained, and informed consent was obtained. Non-fasting blood was collected and sent to the institutional laboratory for the homocysteine level analysis. Patients demographics like age, gender, smoking status, and comorbidities (diabetes mellitus, hypertension) were asked by the researcher and entered in the questionnaire. Vitamin B12 level was not checked.

Data analysis

Data was entered and analyzed on SPSS version 17 (SPSS Statistics, Chicago, US). Mean and the standard deviation were calculated for age, weight, height, body mass index (BMI), and homocysteine level. Frequency and percentage for gender, diabetes mellitus (DM), hypertension (HTN) and smoking status, and correlation coefficient of homocysteine level and age were also calculated. Effect modifiers like gender, BMI, DM, and HTN were controlled through stratification, the Chi-square test was applied, and p-value ≤0.05 was considered as significant.

Results

The mean age of the patients was 55.60 years, with a standard deviation of 11.45 years (n=178). The minimum age of the patients was 40 years, while the maximum age of the patients was 75 years. There were 64 (36%) patients with <50 years of age, while 114 (64%) patients with ≥50 years of age, as shown in Figure 1.

Figure 1. Age groups.

Figure 1

The gender distribution showed 111 (62.40%) male and 67 (37.60%) female, as shown in Figure 2.

Figure 2. Gender distribution.

Figure 2

The mean weight was 66.92 kg, with a standard deviation of 5.71 kg (n=178). The minimum weight of the patients was 56 kg, while the maximum weight of the patients was 83 kg. The mean height was 1.58 meters, with a standard deviation of 0.04 meters (n=178). The minimum height of the patients was 1.50 meters, while the maximum height of the patients was 1.74 meters. 

The mean BMI was 25.01 kg/m2, with a standard deviation of 5.05 kg/m2 (n=178). The minimum BMI of the patients was 24 kg/m2, while the maximum BMI of the patients was 33 kg/m2. There were 150 (84.30%) patients with <30 kg/m2 BMI, and 28 (15.70%) patients were present with ≥30 kg/m2 BMI as shown in Figure 3.

Figure 3. BMI.

Figure 3

BMI - body mass index

The DM, HTN, and smoking status were 58 (32.60%), 96 (53.90%), and 53 (29.80%), respectively, as shown in Figure 4-6.

Figure 4. DM.

Figure 4

DM - diabetes mellitus

Figure 6. Smoking status.

Figure 6

Figure 5. HTN.

Figure 5

HTN - hypertension

The mean homocysteine level was 14.61 micromol/l with a standard deviation of 1.47 (n=178; min 12, max 17). Most of the patients were presented with <15 homocysteine level, i.e., 112 (62.90%), as shown in Figure 7.

Figure 7. Homocysteine level.

Figure 7

A statistically insignificant correlation among homocysteine level and age was calculated by applying Pearson’s correlation test, as shown in Table 1.

Table 1. Correlation of homocysteine level with age (n=178).

  Age Homocysteine level
  Age Pearson’s correlation 1 0.21
p-value   0.778
Homocysteine level Pearson’s correlation 0.21 1
p-value 0.778  

Stratification was done to see the effects of gender, BMI, DM, and HTN on homocysteine levels. Chi-square test was applied, and statistically sufficient evidence of significant relationship was observed in DM (p=0.002) and HTN (p=0.008), as shown in Tables 2-5.

Table 2. Comparison of homocysteine level with gender (n=178).

  Gender Homocysteine  level Total p-value
<15 ≥15
Male 66 (59.5) 45 (40.5) 111 (100) 0.263  
Female 46 (68.7) 21 (31.3) 67 (100)
Total 112 (62.9) 66 (37.1) 178 (100)

Table 5. Comparison of homocysteine level with HTN (n=178).

HTN - hypertension

  HTN Homocysteine  level Total p-value
<15 ≥15
Yes 69 (71.9) 27 (28.1) 96(100) 0.008
No 43 (52.4) 39 (47.6) 82 (100)
Total 112 (62.9) 66 (37.1) 178 (100)

Table 3. Comparison of homocysteine level with BMI (n=178).

BMI - body mass index

  BMI Homocysteine  level Total p-value
<15 ≥15
<30 97 (64.7) 53 (35.3) 150 (100)   0.291  
≥30 15 (53.6) 13 (46.4) 28 (100)
Total 112 (62.9) 66 (37.1) 178 (100)

Table 4. Comparison of homocysteine level with DM (n=178).

DM - diabetes mellitus

DM Homocysteine  level Total p-value
<15 ≥15
Yes 46 (79.3) 12 (20.7) 58 (100) 0.002  
No 66 (55.) 54 (45) 120 (100)
Total 112 (62.9) 66 (37.1) 178 (100)

Discussion

This study showed that there is no significant correlation between serum homocysteine levels and the age of patients with ischemic stroke as per Pearson's correlation test, with a mean homocysteine level of 14.61 and a standard deviation of 1.47 but diabetes mellitus and hypertension are significantly associated with increased homocysteine levels. 

Dutch researchers have found that high homocysteine ​​levels are associated with significantly higher risks of stroke and heart attack. Their study included 7,983 elderly patients whose homocysteine ​​levels were measured in July 1993. In December 1994, 120 had a stroke, and 104 had a heart attack. Researchers have found that the risk of stroke and heart attack increases linearly with increasing homocysteine ​​levels, so an increase of 1 mmol/l at homocysteine ​​levels is associated with a 6-7% increase in the risk of stroke or heart attack. Participants in the study with the highest homocysteine ​​levels had twice the risk of stroke compared with participants with the lowest homocysteine ​​levels after adjusting for age, sex, smoking, high blood pressure, cholesterol, and diabetes. The increased risk of stroke is seen in both ischemic and hemorrhagic strokes and is increased in the presence of high blood pressure. It is interesting to note that the annual stroke rate in the group was 1.0% [17].

Previous research also showed that patients with homocysteine ​​levels greater than 14.2 mmol/l had a stroke rate of 82% higher than participants with a level of 9.25 mmol/l or less after ten years of study. Interestingly, the mean annual stroke rate among study participants (mean age of 70 years) was 0.8% [18].

Swiss researchers have observed a strong relationship between coronary artery disease and high homocysteine ​​levels. They found that an increase of only 5 mmol/l was in accordance with an increased risk of coronary artery disease by 60% in men and 80% in women. They also found that homocysteine ​​levels in 631 patients undergoing angiography increased linearly from 9.2 mmol/l in patients without coronary artery disease to 12.4 mmol/l in patients with the three-vessel disease [19].

Taiwanese and Italian researchers have found a strong relationship between high homocysteine ​​levels and the presence of endothelial dysfunction and atherosclerosis. Not surprisingly, they also reported that high protein foods would significantly increase homocysteine ​​levels. Fortunately, they also found that supplementing the five-week vitamin B cocktail significantly reduced the increase in protein-induced hyperhomocysteinemia [20, 21].

Researchers at the Boston University School of Medicine report that people with homocysteine ​​levels above 14 mmol/l are almost twice as likely to develop Alzheimer's disease as people with lower levels. They also found that an increase in homocysteine ​​levels of 5 mmol/l was associated with a 40% increase in Alzheimer's disease risk [22]. This neurodegenerative damage of homocysteine can be due to its direct neurotoxic effect and its role in endothelial injury [23].

Conclusions

The increase of homocysteine ​​level with age, its role ​​as a risk factor for stroke, coronary artery disease, and neurodegenerative diseases such as Alzheimer's, and its association with diabetes mellitus and hypertension still needs more comprehensive analysis. Studies are also needed to determine the benefits of using homocysteine ​​levels as a screening tool in the elderly for strokes, ischemic heart disease, and neurodegenerative diseases, especially in diabetics and hypertensives, so that strategies can be devised to prevent them earlier with food supplements such as folic acid, vitamin B6 and vitamin B12, and other timely interventions.

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The authors have declared that no competing interests exist.

Human Ethics

Consent was obtained by all participants in this study. College of Physicians and Surgeons Pakistan, Research Evaluation Unit issued approval 14393

Animal Ethics

Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue.

References

  • 1.Homocysteine and thrombosis: from basic science to clinical evidence. Undas A, Brozek J, Szczeklik A. Thromb Haemost. 2005;94:907–915. doi: 10.1160/TH05-05-0313. [DOI] [PubMed] [Google Scholar]
  • 2.TDAG51 is induced by homocysteine, promotes detachment-mediated programmed cell death, and contributes to the development of atherosclerosis in hyperhomocysteinemia. Hossain GS, van Thienen JV, Werstuck GH, et al. J Biol Chem. 2003;278:30317–30327. doi: 10.1074/jbc.M212897200. [DOI] [PubMed] [Google Scholar]
  • 3.Role of hyperhomocysteinemia in endothelial dysfunction and atherothrombotic disease. Austin RC, Lentz SR, Werstuck GH. Cell Death Differ. 2004;11:56–64. doi: 10.1038/sj.cdd.4401451. [DOI] [PubMed] [Google Scholar]
  • 4.Vascular pathology of homocysteinemia: implications for the pathogenesis of arteriosclerosis. McCully KS. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2013581/ Am J Pathol. 1969;56:111–128. [PMC free article] [PubMed] [Google Scholar]
  • 5.Homocysteine and risk of ischaemic heart disease and stroke. A meta-analysis. The Homocysteine Studies Collaboration. JAMA. 2002;288:2015–2022. doi: 10.1001/jama.288.16.2015. [DOI] [PubMed] [Google Scholar]
  • 6.Homocysteine and cardiovascular disease: evidence on causality from a meta-analysis. Wald DS, Law M, Morris JK. BMJ. 2002;325:1202. doi: 10.1136/bmj.325.7374.1202. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Elevated plasma homocysteine in acute stroke was not associated with severity and outcome: stronger association with small artery disease. Perini F, Galloni E, Bolgan I, et al. Neurol Sci. 2005;26:310–318. doi: 10.1007/s10072-005-0505-7. [DOI] [PubMed] [Google Scholar]
  • 8.Serum total homocysteine concentrations and risk of stroke and its subtypes in Japanese. Iso H, Moriyama Y, Sato S, et al. Circulation. 2004;109:2766–2772. doi: 10.1161/01.CIR.0000131942.77635.2D. [DOI] [PubMed] [Google Scholar]
  • 9.Association between high homocyst (e) ine and ischemic stroke due to large- and small-artery disease but not other etiologic subtypes of ischemic stroke. Eikelboom JW, Hankey GJ, Anand SS, Lofthouse E, Staples N, Baker RI. Stroke. 2000;31:1069–1075. doi: 10.1161/01.str.31.5.1069. [DOI] [PubMed] [Google Scholar]
  • 10.Hyperhomocyst(e)inemia and risk of ischemic stroke among young Asian adults. Tan NC, Venketasubramanian N, Saw SM, Tjia HT. Stroke. 2002;33:1956–1962. doi: 10.1161/01.str.0000021899.08659.c8. [DOI] [PubMed] [Google Scholar]
  • 11.Plasma homocyst (e) ine concentrations and the risk of subtypes of cerebral infarction. The Hisayama study. Shimizu H, Kiyohara Y, Kato I, et al. Cerebrovasc Dis. 2002;13:9–15. doi: 10.1159/000047739. [DOI] [PubMed] [Google Scholar]
  • 12.Mild hyperhomocysteinemia is a risk-factor in all etiological subtypes of stroke. Parnetti L, Caso V, Santucci A, et al. Neurol Sci. 2004;25:13–17. doi: 10.1007/s10072-004-0219-5. [DOI] [PubMed] [Google Scholar]
  • 13.Elevated plasma homocysteine was associated with hemorrhagic and ischemic stroke, but methylenetetrahydrofolate reductase gene C677T polymorphism was a risk factor for thrombotic stroke: a Multicenter Case-Control Study in China. Li Z, Sun L, Zhang H, et al. Stroke. 2003;34:2085–2090. doi: 10.1161/01.STR.0000086753.00555.0D. [DOI] [PubMed] [Google Scholar]
  • 14.Homocysteine and its relationship to stroke subtypes in a UK black population: the South London ethnicity and stroke study. Khan U, Crossley C, Kalra L, et al. Stroke. 2008;39:2943–2949. doi: 10.1161/STROKEAHA.107.513416. [DOI] [PubMed] [Google Scholar]
  • 15.Relevance of plasma levels of free homocysteine and methionine as risk predictors for ischemic stroke in the young. Rudreshkumar KJ, Majumdar V, Nagaraja D, Christopher R. Clin Nutr. 2018;37:1715–1721. doi: 10.1016/j.clnu.2017.07.005. [DOI] [PubMed] [Google Scholar]
  • 16.The current status of homocysteine as a risk factor for cardiovascular disease: a mini review. Chrysant SG, Chrysant GS. Expert Rev Cardiovasc Ther. 2018;16:559–565. doi: 10.1080/14779072.2018.1497974. [DOI] [PubMed] [Google Scholar]
  • 17.Homocysteine and short-term risk of myocardial infarction and stroke in the elderly: the Rotterdam Study. Bots ML, Launer LJ, Lindemans J, et al. Arch Intern Med. 1999;159:38–44. doi: 10.1001/archinte.159.1.38. [DOI] [PubMed] [Google Scholar]
  • 18.Nonfasting plasma total homocysteine levels and stroke incidence in elderly persons. Bostom AG, Rosenberg IH, Silbershatz H, et al. Ann Intern Med. 1999;131:352–355. doi: 10.7326/0003-4819-131-5-199909070-00006. [DOI] [PubMed] [Google Scholar]
  • 19.Association of plasma homocysteine with the number of major coronary arteries severely narrowed. Schnyder G, Pin R, Roffi M, Flammer Y, Hess OM. Am J Cardiol. 2001;88:1027–1030. doi: 10.1016/s0002-9149(01)01983-x. [DOI] [PubMed] [Google Scholar]
  • 20.Effects of short-term vitamin (folic acid, vitamins B6 and B12) administration on endothelial dysfunction induced by post-methionine load hyperhomocysteinemia. Chao CL, Chien KL, Lee YT. Am J Cardiol. 1999;84:1359–1361. doi: 10.1016/s0002-9149(99)00575-5. [DOI] [PubMed] [Google Scholar]
  • 21.The AFIB report. http://afibbers.org/S/afib68sp.pdf 2007
  • 22.Plasma homocysteine as a risk factor for dementia and Alzheimer’s disease. Seshadri S, Beiser A, Selhub J, et al. N Engl J Med. 2002;346:476–483. doi: 10.1056/NEJMoa011613. [DOI] [PubMed] [Google Scholar]
  • 23.The controversial role of homocysteine in neurology: from labs to clinical practice. Moretti R, Caruso P. Int J Mol Sci. 2019;20:231. doi: 10.3390/ijms20010231. [DOI] [PMC free article] [PubMed] [Google Scholar]

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