Open Access Highly Accessed Research article

Association of iron overload based quantitative T2* MRI technique and carotid intima-media thickness in patients with beta-thalassemia: A cross-sectional study

Shahram Akhlaghpoor1*, Morteza Hoseini2 and Amirhosein Jafarisepehr2

Author Affiliations

1 Noor Medical Imaging Center, Tehran, Iran

2 Department of Radiology, Tehran University of Medical Sciences, Sina Hospital, Tehran, Iran

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BMC Cardiovascular Disorders 2010, 10:62  doi:10.1186/1471-2261-10-62

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2261/10/62


Received:14 July 2010
Accepted:31 December 2010
Published:31 December 2010

© 2010 Akhlaghpoor et al; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Body iron status has been implicated in atherosclerotic cardiovascular disease. The main hypothesis is that high iron status is associated with increased risk of atherosclerosis. We investigated the potential role of iron as an additional risk factor promoting atherosclerosis among beta-thalassemic patients.

Methods

In this cross-sectional study, the liver iron load was assessed by quantitative T2* MRI technique and intima-media thickness (IMT) of the common carotid artery by high-resolution ultrasound among 119 patients (62 male, 57 female) with beta-thalassemia (major and intermediate) whose age ranged from 10 to 50 years with a mean of 25.6 years. The patients were divided into three groups according to the severity of iron loading, obtained by T2*MRI technique: group I (normal), group II (mild) and group III (moderate and severe) iron load.

For elimination of the effect of age on carotid IMT values, the patients also were divided into four age groups (10-19 y, 20-29 y, 30-39 y and 40-50 y). Mean carotid IMT based on the severity of iron loading were compared at different age groups, using one way ANOVA analysis for assessing the effect of iron loading on carotid IMT. Pearson's coefficient of correlation were used to assess the degree of correlation between studied variables (liver T2*, IMT, age).

Results

There were significant differences in mean carotid IMT based on the severity of iron loading at different age groups, with P = 0.003 at 20-29 y, P = 0.006 at 30-39 y and p = 0.037 at 40-50 y. Age (p = 0.001) and liver T2*(p = 0.003) had significant correlation with mean carotid IMT independently.

At the age group of 10-19 years, there were not significant differences in mean carotid IMT based on the liver iron loading (p = 0.661).

No significant differences also are seen in mean carotid IMT between male and female (p = 0.41).

Conclusions

This study identified a relationship between body iron status and carotid IMT. This relationship support to the hypothesis of a link between body iron load and atherosclerosis.

Background

Thalassemia is considered the most common genetic disorder worldwide[1]. It is result from a defect in the synthesis of one or more of the subunits of hemoglobin.

In b-thalassemia, the b-chains of hemoglobin have a normal structure but are produced in reduced or undetectable amounts, resulting in excess of α-chains, which are unstable and precipitate to form intracellular inclusion bodies. This excessive intracellular deposition of α-chain material is responsible for peripheral hemolysis of the erythrocytes [2-4]. Conventional treatment of the patients with b-thalassemia major is repeated blood transfusions.

Repeated blood transfusions and peripheral hemolysis leads to iron overload initially in reticulo-endothelial system and secondary to all parenchymal organs, mainly heart, pancreas, pituitary gland, and gonads, with cytotoxic effects [5].

Accumulation of iron in excess of physiologic requirements has been implicated in risk of cardiovascular disease, because of the catalytic role of iron in free radical reactions, cause oxidative stresses on vessel wall [6-8].

Increased common carotid IMT is a marker of early atherosclerosis and has been associated with cardiovascular risk and risk of coronary artery disease events [9,10].

First, Sullivan in 1981 formulated the iron-heart hypothesis of atherosclerotic cardiovascular disease. According to this hypothesis, the loss of iron with menstruation explains the lower risk of coronary heart disease(CHD) in premenopausal women compared with men and postmenopausal women [11].

This, accompanied by the observation that hysterectomy without oophorectomy was associated with an increased CHD risk [12,13].

Strong epidemiological evidence is available that iron is an important factor in the process of atherosclerosis. But some studies do not support the role of iron as a potent risk factor in CHD and the role of iron in promotion of atherogenesis remains controversial [13,14].

An explanation for these discrepant results may lie in the limitations of the different markers that were used for iron load assessing, for example, serum iron and transferrin saturation are affected by inflammation and diurnal variation and serum ferritin levels is affected by factors, such as chronic inflammatory and Infectious disease, hematological and other malignancies and liver dysfunction [5,15].

Therefore, it is quite possible that the levels of serum ferritin are influenced by inflammation independently of iron stores [16,17].

This may explain the failure of some previous studies find an association between ferritin and CHD.

The liver iron concentration (LIC) is a reliable indicator of total body iron stores in thalassemic patients [18]. MRI measures the LIC indirectly by detecting the paramagnetic effect produced by iron deposition. Deposition of iron in the liver increases the magnetic field heterogeneities, resulting in a decreased T2* relaxation value of the liver that leads to a decline in liver MRI signal, proportionally to the amount of the LIC [19,20].

This method (T2*MRI) is a quantitative, non-invasive, accurate, widely available and reproducible method for estimating iron over load in different tissues [21,22].

Therefore, in this study we were used from quantitative T2*MRI technique, for estimation of the liver iron stores (as the indicator of body iron load).

The purpose of this study was to evaluate the role of iron as a potent risk factor in early atherosclerosis.

Methods

Subjects

In this cross-sectional study, we enrolled 119 patients (62 male, 57 female) with beta -thalassemia major and intermediate that referred from the hematology clinic for routine assessment of the liver iron load by MRI imaging.

The patient's age ranged from 10 to 50 years with a mean of 25.6 years.

All of the patients had been received chelation therapy with subcutaneous deferoxamine. Smokers and patients with heart failure, previous history of cardiovascular event, systemic hypertension, diabetes mellitus, hyperlipidemia, and thyroid dysfunction were excluded, to eliminate the effect of these factors on carotid IMT.

The patients based on the compliance, to chelation therapy had different liver iron load.

Liver iron load was determined by quantitative T2* MRI technique and the patients based on the severity of iron loading were divided into three groups: group I (normal), group II (mild) and group III (moderate and severe) iron load. Severity of iron loading is defined as follows:

MRI T2* values greater than 6.3 ms was categorized as normal (T2* > 6.3 ms), mild (2.8-6.3 ms), moderate (1.4-2.7 ms) and severe (T2* < 1.4 ms) [23,24].

Mean carotid IMT were assessed in the right and left common carotid arteries by high-resolution ultrasound in the mentioned groups. To elimination of the effect of age in carotid IMT values, the patients also were divided into four age groups. (10-19 y, 20-29 y, 30-39 y and 40-50 y)

Then mean carotid IMT values based on the liver iron loading were compared at different age groups.

The Institutional Ethics Committee approved the study and all subjects gave informed consent.

MRI protocol

MRI scans were performed with a 1.5 T superconducting MR imager (Siemens Symphony Imager, Erlangen, Germany), using the method described by Anderson et al [21].

A standard quadrature RF body coil was used in all measurements for both excitation and signal detection.

All subjects were placed in a supine position and entered the magnet cradle, using the head-first configuration. Respiratory triggering was used to monitor the patients' breathing. Spatial presaturation slabs were used to suppress motion-related artifacts. The MRI T2* of the liver was determined using a single 10 mm slice through the center of the liver scanned at 12 different echo times (TE 1.3-23 ms).

Each image was acquired during a 11-13 s breath-hold using a gradient-echo sequence (repetition time 200 ms, flip angle 20◦, base resolution matrix 128 pixels, field of view 39.7 × 19.7 cm, sampling bandwidth of 125 kHz).

The signal intensity of the liver parenchyma and the background noise were measured in each of the 12 images, using in-house software (CMR tools, Imperial College). Background noise was subtracted from the liver signal intensity, and the net value was plotted against the echo time for each image. A trend line was fitted to the resulting exponential decay curve, with an equation of the form y = KeTE/T2* where K represents a constant, TE represents the echo time and y represents the image signal intensity.

Carotid ultrasound

Longitudinal B-mode scans of the common carotid artery were obtained, using ALOKA ultrasound system (model prosound α5 sx, company Ltd, Japan) with 10-MHZ linear array transducer. The gain was set at 60-70 dB that was usual in clinical practice. The far wall was assessed just 2 cm proximal to the carotid bifurcation, to identify the maximal IMT, by manually.

IMT defined as the distance between the junction of the lumen and intima and that of the media and adventitia [10,25].

Three measurements were made in the right and left common carotid arteries and were averaged to determine the IMT for each side.

Statistical analyses

Summary of data are presented as mean values ± one standard deviation.

The correlations between parameters (liver T2*, IMT, age) were analyzed, using Pearson's coefficient of correlation. To compare quantitative variables with different groups, one way ANOVA analysis were used.

kruskal-wallis analysis also were used, due to relatively low sample size in this study.

All statistical analyses were assessed using SPSS software for windows ver.18 (SPSS Inc., Chicago, IL, USA). A p-value less than 0.05 was considered statistically significant.

Results

Table 1 shows summary of general characteristics of the patients including age, weight, height, age at diagnosis, transfusion start age, transfusion interval, transfusion volume, deferoxamine start age and mean duration of Chelation therapy.

Table 1. General characteristics of the patients

Table 2 shows Pearson's linear correlation coefficients for simple regression analysis of the carotid IMT with the other parameters (age and liver T2*). Age (as a continuous variable) and liver T2* had significant correlation with mean carotid IMT independently.

Table 2. Pearson's correlation coefficients between the IMT and parameters (age, Liver T2*)

Table 3 shows Mean carotid IMT based on the severity of liver iron loading at different age groups. At the age group of 10-19 years, no significant differences were found in mean carotid IMT based on the iron loading.

Table 3. Mean carotid IMT based on the severity of iron loading at different age groups.

At the other age groups, mean carotid IMT in group III (moderate and severe) was higher than group II (mild) and in group II (mild) was higher than group I(normal). Differences in mean carotid IMT were significant at these age groups based on the iron loading.

With kruskal-wallis analysis, the result was the same and differences in mean carotid IMT were significant in all age groups with exception of 10-19 year; with p = 0.5 at 10-19 y, p = 0.004 at 20-29 y, p = 0.006 at 30-39 y and p = 0.021 at 40-50 y.

Figure 1 shows Line chart of the differences in mean carotid IMT based on the severity of iron loading at different age groups. These differences are lower in the younger patients and increase with relatively exponential curve in the older patients.

thumbnailFigure 1. Line chart of the mean carotid IMT based on the severity of iron load.

No significant differences are seen in mean carotid IMT between male and female. (p = 0.41)

Discussion

Carotid IMT is considered an early marker of atherosclerotic process and is currently used to assess the presence and the progression of atherosclerosis [9,10]. This study finds an association between iron overload and early atherosclerosis as reflected by increased carotid IMT in the thalassemic patients. Our data support the hypothesis that iron is a risk factor of CHD. Epidemiological studies examining the role of iron in cardiovascular disease have yielded conflicting results [9,26]. These conflicting results may due to the use of different indicators of iron stores and their modulation by various factors[9].

Some investigators have hypothesized that iron may be primarily involved in the early events of atherosclerosis, and focusing on cardiovascular morbidity and mortality (reflecting later stage of the disease) may not give insight in to the potential mechanistic role of iron [12,27].

Mentioned reasons explain the failure of some previous studies to finding an association between body iron load and CHD.

At the age group of 10-19 years, no significant differences are seen in mean carotid IMT based on the severity of iron loading. This finding could be resulting from this fact that, atherogenesis is a prolonged process[28] and should not expect to present at early young patients.

In healthy person's, carotid IMT is significantly higher in male in comparison to female [29]. At present study there were not significant differences in mean carotid IMT between male and female, which is in agreement with iron hypothesis. Because in thalassemic patients, body iron load is in the same ranges in male and female. On opposite, in healthy person's body iron load is significantly higher in male in comparison to female.

The mechanism by which iron may stimulate atherogenesis is unclear.

It is suggested that the catalytic role of iron in free radical reactions cause oxidation of LDL and may be an important factor in the formation of atherosclerotic lesions. Studies have shown that iron can stimulate lipid peroxidation in vitro and in vivo [13].

Iron-catalyzed free radical reactions cause oxidation of LDL, which occurs in endothelial cells, smooth muscle cells, lymphocytes, or macrophages.

Normal LDL can cross the arterial wall without causing damage to the vessel wall. Unlike normal LDL, oxidized LDL is recognized by macrophages, followed by accumulation of lipids in these cells and the formation of foam cells, the characteristic cells of the fatty-streak lesions of early Atherosclerosis. Oxidized LDL also has chemotactic activity that provides recruitment of circulating monocytes to the vessel wall and prevents the exiting of macrophages from the intima of the arterial wall.

Thereby, oxidized LDL has cytotoxic capacity that induces changes in endothelial cells with loss of endothelial integrity, which could facilitate further accumulation of both circulating monocytes and LDL and thus promote the progression of the atherosclerotic lesion [13,30-33].

Thalassemic patients have mostly blood lipid levels within the normal range and Prevalence of lipid and lipoprotein abnormalities is much lower as compared to the general population of the same age[34], but carotid IMT is significantly higher in thalassemic patients in comparison with the healthy persons[35]. This subject shows the important role of the body iron store in atherosclerosis process.

The clinical importance of this study is prevention from the progression of atherosclerosis in early stages by decrease in body iron load.

Decrease in body iron load can achieve by good compliance of chelation therapy in the thalassemic patients and by blood donation in healthy persons.

A potential limitation of this study is the cross-sectional and observational nature of our study. This type of study cannot identify a cause-and-effect relationship, but associations can be examine. another limitation is the relative low sample size, especially at the high age groups.

Findings from the current study may be applied to thalassemic patients, but cannot be extrapolated directly to the general population.

Conclusions

In summary, we observed an independent relationship between body iron load and carotid atherosclerosis. Our findings are in agreement with previous results and Support to the hypothesis that iron is linked to cardiovascular disease.

Abbreviations

IMT: intima-media thickness; CHD: coronary heart disease; LIC: liver iron concentration; LDL: Low density lipoprotein; T2* MRI: T2-star Magnetic resonance imaging

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

MH carried out the measurement and acquisition of the MRI and IMT data. AJS conceived of the study, and participated in the design of the study and performed the statistical analysis. SA participated in the design of study and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.

Acknowledgements

The authors would like to thank the patients for their co-operation and participation in the study, and the radiographers at the MR imaging center, for measurement of the magnetic resonance signal intensities; and data acquisition.

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