Re:The role of folic acid on the hyperhomocysteinemia in the Buerger's disease (Thromboangiitis Obliterans)

[문형철]

BEYOND REASON

엽산이 버거씨병 환자의 고호모시스테인 혈증을 치료하지만 버거씨병으로 인한 절단을 방지하지는 못함(6개월 추적검사)

버거씨병 치료법 찾아야

(thromboangitis obliterans)

The role of folic acid on the hyperhomocysteinemia in the Buerger's disease (Thromboangiitis Obliterans)

Ali Akbar Beigi, Mohammad Ali Hoghoughi, [...], and Hassan Masoudpour

Additional article information

Abstract

Background:

The mechanism underlying Buerger's disease (BD) is still unknown. Recently, thrombophilic conditions predisposing to a hypercoagulable state have been hypothesized as triggers for BD. The aim of the study is to eval‎uate the preval‎ence of the hyperhomocysteinemia and level of the anticardiolipin antibodies, and the role of folic acid on the hyperhomocysteinemia and on the rate of the amputations in the patients with BD.

Materials and Methods:

In an experimental placebo-controlled double-blinded study, between 2004 and 2010, thirty patients with BD were randomly assigned into two groups (14 patients in a drug group and 16 patients in the placebo group). Drug or placebo was administered, and they were followed in 2 and 6 months for homocysteine, Anticardiolipin antibodies and the risk of amputations.

Results:

At the beginning of the study homocysteine level was higher than normal in 19 patients (63%). There was a significant decrease in homocysteine level during 6 months in folic acid group (P < 0.001), but there was no change in the placebo group. None of our patients had elevated Anticardiolipin antibodies, and there was no change in the level of Anticardiolipin antibody during study. High level of homocysteine did not associate with more amputations during 6 months of study (P > 0.05).

Conclusion:

This study shows the hyperhomocysteinemia in BD, and the benefit of folic acid treatment in homocysteine lowering, but folic acid doesn’t inhibit the risk of major and minor amputation during 6 months of follow-up. Longer follow-up may reveal the role of folic acid in these patients

Keywords: Anticardiolipin antibodies, Buerger's disease, folic acid, hyperhomocysteinemia, thromboangiitis obliterans

INTRODUCTION

Thromboangiitis Obliterans or Buerger's disease (BD) is a chronic nonatherosclerotic inflammatory obliterative disease which affects predominantly small and medium arteries and veins in the infra-popliteal and infra-brachial regions. Although BD has a worldwide distribution, nowadays it is more preval‎ent in the middle east and far east than in North America and Western Europe.[1,2,3,4] It is seen more common in the young smoker men and in a low socioeconomic status.[5] BD is established on the basis of the clinical presentation and physical findings, according to the following criteria; history of smoking (current or recent), onset of disease before 50 years old, infra-popliteal obliterative arterial involvement, upper limb involvement or phlebitis migrans, and absence of atherosclerosis risk factors other than smoking.[1,2,3,4,6,7,8] There is no specific diagnostic laboratory indicator, so in those countries where the BD is common, the clinical criteria of Shionoya are accepted.[3] However, in countries with a rare incidence of BD, the diagnosis is based on imaging and by excluding other vasculitis, using expensive laboratory tests.

Etiology and pathogenesis of BD is not completely understood, but environmental predisposing factors such as genetic and nicotine was supposed.[1,2,3] After smoking and tobacco cessation, other medical or surgical therapies have limited results.[2,3]

Another possible pathogenesis observed in the patients with BD is a hemostatic disturbance. Hyperhomocysteinemia is common in BD, and may have an important effect on BD pathogenesis irrelevant to Nicotine.[5] Preliminary data have been shown hyperhomocysteinemia is a risk factor for venous thrombosis[9,10] aggravates the prognosis, and may reveal that the patients undergo amputation earlier.[8]

Unfortunately, preval‎ence of smoking is very high in our country, and the preval‎ence of the BD is high as well; in contrast with other Asian countries which encounter one or two new patients per year.[1,3] The patients with BD take two in every 20 vascular surgery beds at St. Zahra Hospital. About 23% of the ischemic patients <50 years old who referred to our vascular clinic are diagnosed with Burger's disease. Also, we see many complications related to disease as a result of late diagnosis and treatment, but many of our patients could not stop smoking, and have no ideal treatment response.

It has been hypothesize that hypercoagulability state (like hyperhomocysteinemia, increased anticardiolipin, and genetic factors) has a role in the pathophysiology of BD.[8,9,11,12,13,14] It has been established that Folic acid could improve hyperhomocysteinemia;[15,16] Also Folic acid could improve endothelial function as a result of lowering homocysteine, and might have a beneficial effect on BD. This study was done to eval‎uate the role of homocysteine lowering effect of Folic acid on limb amputation, the major complication of BD.

MATERIALS AND METHODS

This was an experimental placebo controlled double-blinded study. The study group was 30 identified Buerger's patients based on the criteria who were randomly allocated in drug or placebo groups (14 patients in drug group and 16 patients in placebo group) from January 2004 to January 2010. All of them were advised stop smoking and were on standard routine treatment protocol of BD. To confirm‎ the smoking cessation, urine check was done. All participants signed informed consent. The study was approved by Isfahan University of Medical Sciences Ethics Committee, Isfahan, Iran. It was registered in Iranian Registry of Clinical trials (IRCT201108012106N2).

The inclusion criteria contained negative history of hypertension, diabetes mellitus, ischemic heart disease, cerebrovascular disease or collagen vascular disease as well as negative vasculitis workup. The exclusion criteria were surgical sympathectomy or any sort of vascular bypass; using aspirin, calcium channel blocker, B6 or B12; stop smoking during the study and have not compliance of being treated. Also, patients with hypercoagulative state due to inherited thrombophilia (factor V Leiden, A202120G prothrombin variant, acquired activated protein C resistance, protein C and S deficiency, antithrombin deficiency were excluded from the study.

Medication was one oral 5 mg folic acid tablet (Jallinus Pharmacy, Tehran, Iran) and placebo (Amin Pharmacy, Isfahan, Iran) with the same as the color, size, weight, and box.

At the start of the study, we measured demographic data, homocysteine and Anticardiolipin level in the form. Following administration of drug and placebo, they were followed 2 and 6 months later. Lab data, minor or major amputations were recorded during follow-up.

At the end of the study, data were analyzed by SPSS version 17 (SPSS Inc., Chicago, USA) by Chi-square, t-test, covariance analysis, repeated measure ANOVA, Freidman, Wilkaxon and Mann–Whitney tests.

RESULTS

This study contained 30 patients (14 in Folic acid group and 16 in the placebo group) [Table 1]. All of them were male. None of the patients had a history of diabetes mellitus, chronic renal failure, ischemic heart disease, and hypertension. Only two patients had a history of hyperlipidemia. Except years of education, other baseline characteristics didn’t have a difference between two groups (P > 0.05).

Table 1

Demographic parameters in two groups

At the beginning of the study, 19 patients (63%) had homocysteine level higher than normal (normal value was 15 mg/dl). None of our patients had elevated anticardiolipin antibody. By one sample t-test, baseline homocysteine level at baseline was more than normal value in Buerger's patients (P = 0.002). The Baseline level of homocysteine and anticardiolipin antibody was not different between two groups (P > 0.05) [Tables ​[Tables22 and ​and33].

Table 2

The mean of homocysteine level at the baseline, 2nd and 6th month of study

Table 3

The mean of anticardiolipin level at the baseline, 2nd and 6th months

Because the baseline of the homocysteine level was higher in folic acid group (that was not significant), covariance analysis was performed, and it demonstrated that the folic acid was more effective from the 2nd month of study.

We divided the patients into two normal and high level of homocysteine groups; and compared the major and minor limb amputations in each placebo and folic acid groups at the beginning, 2nd and 6th month. High level of homocysteine did not increase amputations during 6 months of study (P > 0.05) [Table 4]. Anticardiolipin antibody did not change in level during 6 months of study in none of the folic acid and placebo groups (P > 0.05).

Table 4

The number of major and minor amputation in both groups

DISCUSSION

This study revealed 63% preval‎ence of hyperhomocysteinemia in our Buerger's patients that was higher than previous reports, which was 23% in Stammlers study[3] and 60% in Deiham study.[8]

This study have been shown the benefit of folic acid on homocysteine lowering in Buerger's disease but not on Anticardiolipin level. The studies show 10 mg folic acid for 4 weeks in patients with hyperhomocysteinemia (more than 75 percentile) and without cardiovascular risk factors could improve arterial endothelial function and decrease homocysteine.[9] There was no change for independent endothelial vasodilatation. No side effect had been reported.[1,9]

Two studies had been shown that endothelial function didn’t improve with homocysteine lowering;[3,14] but another one revealed the lower homocysteine is a protective vascular factor irrelevant to folate.[8,10,15] Impaired endothelial function is assumed as a predisposing factor in BD[1,2] and we hypothesized that the folic acid may improve vasculature endothelium and could decrease amputation. In present study, high level of homocysteine did not associate with more amputations after 6 months of study in either placebo or folic acid group; and we could not follow our supposition. This pilot result can be attributed to short follow-up or small sample size.

As in our results, previous studied revealed folic acid, Vitamin B6 and B12 could not inhibit major cardiovascular complications and recurrent venous thrombosis.[1,8,11,12,15,17]

CONCLUSION

This study shows hyperhomocysteinemia in BD, and the benefit of folic acid in homocysteine lowering; folic acid could not inhibit major and minor amputation during 6 months of follow-up. Longer follow-up may reveal the benefit of folic acid in these patients.

This study emphasized the role of homocysteine in the pathogenesis of BD, especially in smoker patients. More detailed immunological and endothelial surveys can clarify this hypothesis.

AUTHOR'S CONTRIBUTION

All authors have contributed in designing and conducting the study. All authors have assisted in preparation of the first draft of the manuscript or revising it critically for important intellectual content. All authors have read and approved the content of the manuscript and confirmed the accuracy or integrity of any part of the work.

ACKNOWLEDGMENT

We thank Dr. Maryam Ghassami for her collaboration in preparing the proposal of the study.

Footnotes

Source of Support: Nil

Conflict of Interest: None declared.

Article information

J Res Med Sci. 2014 Nov; 19(11): 1034–1037. 

PMCID: PMC4310074

PMID: 25657746

Ali Akbar Beigi, Mohammad Ali Hoghoughi,1 Afrooz Eshaghian,2 Akbar Hassan Zade,3and  Hassan Masoudpour4

Department of Vascular Surgery, Saint Al-Zahra Hospital, Isfahan University of Medical Sciences, Isfahan, Iran

1Department of Surgery, Saint Al-Zahra Hospital, Isfahan University of Medical Sciences, Isfahan, Iran

2Department of Head and Neck Surgery, Saint Al-Zahra Hospital, Isfahan University of Medical Sciences, Isfahan, Iran

3Department of Epidemiology and Biostatistics, Isfahan University of Medical Sciences, Isfahan, Iran

4Molecular Structure and Function, Research Institute, The Hospital for Sick Children, University of Toronto, Ontario, Canada

Address for correspondence: Dr. Mohammad Ali Hoghoughi, Department of Surgery, Saint Al-Zahra Hospital, Isfahan University of Medical Sciences, Isfahan, Iran. E-mail: moc.oohay@amihguohgoh

Received 2014 Mar 7; Revised 2014 Sep 13; Accepted 2014 Nov 17.

Copyright : © Journal of Research in Medical Sciences

This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Articles from Journal of Research in Medical Sciences : The Official Journal of Isfahan University of Medical Sciences are provided here courtesy of Wolters Kluwer -- Medknow Publications

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