Original Research Article

Endothelial function, antioxidant status and vascular compliance in

newly diagnosed HFE C282Y homozygotes
William J. Cash
a,
*, Stephen ONeill
b
, Mark E. ODonnell
b
, David R. McCance
c
,
Ian S. Young
d,e
, Jane McEneny
e
, Neil I. McDougall
a
, Michael E. Callender
a
a
Department of Hepatology (Liver Unit), Royal Victoria Hospital, Belfast, UK
b
Department of Vascular and Endovascular Surgery, Royal Victoria Hospital, Belfast, UK
c
Department of Endocrinology and Diabetes, Royal Victoria Hospital, Belfast, UK
d
Department of Clinical Biochemistry, Royal Victoria Hospital, Belfast, UK
e
Department of Medicine, Queens University Belfast, Belfast, UK
1. Introduction
Iron overload in HFE haemochromatosis causes deranged liver
enzymes. Venesection is the optimal treatment for HFE haemo-
chromatosis where improvement of liver enzymes and reversal of
hepatic brosis have been reported [1,2]. Elevated iron levels in
HFE haemochromatosis patients are known to be associated with
increased oxidative stress. Kom et al. [3] demonstrated increased
urinary isoprostanes and reduced vitamin A levels in iron
overloaded HFE haemochromatosis patients. Following venesec-
tion and normalisation of iron levels, they reported a signicant
reduction in urinary isoprostanes (245 pg/mg creatinine vs.
146 pg/mg creatinine, p < 0.001) and a signicant increase in
vitamin A (0.34 mg/ml vs. 1.36 mg/ml, p = 0.035) suggesting a
reduction in oxidative stress [3].
Norris et al. [4] provided evidence of endothelial dysfunction in
HFE haemochromatosis. Their comparison of adhesion molecule
expression between 139 subjects with HFE C282Y haemochroma-
tosis and 27 healthy controls identied signicantly higher sICAM
(p = 0.0059) and E-selectin (p = 0.0006) as well as signicantly
lower L-selectin (p = 0.0002) levels in HFE haemochromatosis.
Other researchers have also associated elevated iron and reduc-
tions in ascorbate in HFE haemochromatosis patients with an
improvement in ascorbate noted following venesection [5,6].
This decrease in isoprostane production combined with an
improved anti-oxidant status following venesection suggests an
overall reduction in lipid peroxidation and antioxidant consump-
tion following vensection. This pilot study was aimed to establish
Advances in Medical Sciences 59 (2014) 2833
A R T I C L E I N F O
Article history:
Received 16 January 2013
Accepted 1 July 2013
Available online 15 March 2014
Keywords:
Antioxidant
Compliance
Haemochromatosis
Vascular
A B S T R A C T
Purpose: This pilot study was aimed to establish techniques for assessing and observing trends in
endothelial function, antioxidant status and vascular compliance in newly diagnosed HFE haemochro-
matosis during the rst year of venesection.
Patients/methods: Untreated newly diagnosed HFE haemochromatosis patients were tested for baseline
liver function, iron indices, lipid prole, markers of endothelial function, anti-oxidant status and vascular
compliance. Following baseline assessment, subjects attended at 6-weeks and at 3, 6, 9 and 12-months
for follow-up studies.
Results: Ten patients were recruited (M= 8, F = 2, mean age = 51 years). Venesection signicantly
increased high density lipoproteins at 12-months (1.25 mmol/L vs. 1.37 mmol/L, p = 0.01). However,
venesection did not signicantly affect lipid hydroperoxides, intracellular and vascular cell adhesion
molecules or high sensitivity C-reactive protein (0.57 mmol/L vs. 0.51 mmol/L, p = 0.45, 427.4 ng/ml vs.
307.22 ng/ml, p = 0.54, 517.70 ng/ml vs. 377.50 ng/ml, p = 0.51 and 290.75 mg/dL vs. 224.26 mg/dL,
p = 0.25). There was also no signicant effect of venesection on anti-oxidant status or pulse wave velocity
(9.65 m/s vs. 8.74 m/s, p = 0.34).
Conclusions: Venesection signicantly reduced high density lipoproteins but was not associated with
signicant changes in endothelial function, anti-oxidant status or vascular compliance. Larger studies
using this established methodology are required to clarify this relationship further.
2014 Medical University of Bialystok. Published by Elsevier Urban & Partner Sp. z o.o. All rights
reserved.
* Corresponding author at: Department of Hepatology (Liver Unit), Royal Victoria
Hospital, 1st Floor, East Wing, Grosvenor Road, Belfast, UK. Tel.: +44 28 9063 3529;
fax: +44 28 9063 4022.
E-mail address: [email protected] (William J. Cash).
Contents lists available at ScienceDirect
Advances in Medical Sciences
j ou r n al hom epage: www. el s evi er . co m/ l ocat e/ advms
1896-1126/$ see front matter 2014 Medical University of Bialystok. Published by Elsevier Urban & Partner Sp. z o.o. All rights reserved.
http://dx.doi.org/10.1016/j.advms.2013.07.001
techniques for assessing and observing trends in serological
endothelial function, antioxidant status and vascular compliance
in newly diagnosed HFE haemochromatosis subjects during the
rst year of venesection.
2. Patients and methods
2.1. Patient recruitment
Newly diagnosed HFE haemochromatosis patients, between the
ages of 20 and 75, who had not previously undergone venesection,
were recruited. HFE haemochromatosis was dened by the
phenotypic pattern of raised ferritin (at time of recruitment or
at some time in the past) in combination with homozygosis for HFE
C282Y. Patients with known hypertension (blood pressure >160/
90 mm Hg), diabetes mellitus, a history of cardiovascular disease
and those taking lipid lowering agents or hormonal preparations
were excluded. Written informed consent was obtained.
2.2. Clinical intervention venesection
Following initial assessment, patients were enrolled in a standard
venesection programme where fortnightly phlebotomy of one unit
of whole blood (approx. 400 ml) was performed. At the time of this
study the target ferritin and iron saturations of the initial phase of
the venesection programme were 100 mg/L and 50% respectively.
Fortnightly venesection continued until these targets were achieved
then the venesection interval increased to three monthly.
2.3. Patient assessment
2.3.1. Baseline clinical parameters
Following completion of initial baseline examinations and
investigations at recruitment, patients subsequently attended at 6-
weeks and at 3, 6, 9 and 12-months for follow-up. Blood pressure
(mm Hg) and body mass index [BMI = weight (kg) divided by
height (metres) squared] were recorded after an overnight fast
followed by serological assessment of endothelial dysfunction and
anti-oxidant status.
2.4. Biochemical assessment
2.4.1. Blood sampling
Fasting peripheral venous blood samples for plasma glucose,
serum lipid proles, liver function tests and iron studies were
performed routinely at each assessment time-point. For serological
assessment of endothelial dysfunction and anti-oxidant status,
plasma samples for ascorbate were centrifuged immediately while
serum collected for all other assays was clotted for 15 min and then
centrifuged. All samples were transferred to 2 ml tubes (Sarstedt,
Ireland) and stored at 80 8C. All commercial assay analyses were
performed according to the manufacturers guidelines. Intra- and
inter-assay coefcients of variation were within satisfactory limits
according to the manufacturers guidelines.
2.4.2. Plasma lipid hydroperoxides
These were measured spectrophotometrically using the Ferrous
Oxidation-Xylenol Orange-version 1-assay (FOX 1) which was used
to determine hydroperoxides (HPO) in the aqueous phase of serum.
Hydroperoxides oxidise ferrous ions to ferric ions in dilute acids and
the resultant ferric ions were then determined using ferric sensitive
dyes as an indirect measure of hydroperoxide concentration.
2.4.3. Intracellular and vascular cell adhesion molecules
Plasma soluble intercellular adhesion molecule-1 (sICAM-l) and
soluble vascular cell adhesion molecule-1 (sVCAM-l) were
measured using commercially available ELISA kits from Eli-pair
(Diaclone, Besancon, France).
2.4.4. Ascorbate
Concentrations were determined by the enzymatic oxidation of
ascorbic acid and subsequent quinoxaline formation to generate a
uorescent derivative measured on the Cobas Fara centrifugal
analyser as described by Vuilleumier et al. [7].
2.4.5. Lipid soluble antioxidants
These levels were measured using a high performance liquid
chromatography technique (HPLC) using diode array detection to
assess retinol, g-tocopherol, a-tocopherol, lutein, zeaxanthin, b-
cryptoxanthin, a-carotene, b-carotene and lycopene according to
the method of Craft and Soares [8]. The detection limits for retinol
and the tocopherols were 0.05 nmol/l while 0.005 nmol/l was used
for carotenoids.
2.4.6. High-sensitive C-reactive protein
This was measured with a latex-enhanced immunoturbidi-
metric assay (Randox Pharmaceuticals, Curmlin) using an ILab 600
biochemical analyzer and ILab 600 computer software (Instru-
mentation Laboratories, Warrington).
2.5. Estimation of vascular compliance
The methodologies of pulse wave analysis (PWA) and pulse
wave velocity (PWV) gated to the cardiac cycle have previously
been described [911]. After rest in the supine position in a
temperature controlled room for a minimum of 15 min, radial
pulse wave analysis was recorded with a Millar tonometer and the
Sphygmocor system model SCORPx, incorporating the pulse wave
velocity system Model SCOR-Vx (SPC-301; Millar instruments and
Atcor medical, Sydney, Australia). For PWA, triplicate measure-
ments were made in the supine position from the radial artery of
the dominant arm and the average calculated. The Sphygmocor
analysis software automatically processed the radial artery
waveform data and using a generalised transfer function generated
measures of vascular compliance including augmentation index
calibrated to 75 beats per minute (AgIx75), time to reectance (TR),
Buckbergs subendocardial viability ratio (SEVR) and ejection
duration percentage (ED%). Calculation of PWV was similar to PWA
with the analysis gated to the cardiac cycle with separate readings
from the dominant radial artery (distal site) and ipsilateral carotid
artery (proximal site). Carotid-radial PWV was measured rather
than carotid-femoral due to ease of reproducibility and accept-
ability to patients.
2.6. Statistical analysis
Analyses were performed using the Statistical Programme for
Social Sciences (SPSS 15.0 for windows; SPSS Inc., Chicago, IL, USA).
Due to the small number of subjects, non-parametric analysis was
undertaken with Friedman repeated measure analysis. Where the
Friedman test demonstrated signicance (p < 0.05) or where
trends were observed, further analysis with Wilcoxon signed-rank
test was performed to establish when the difference occurred
during the study period.
3. Results
3.1. Patient demographics
Ten patients with HFE haemochromatosis were recruited
(male = 8, female = 2, mean age = 51 13 years, mean systolic
blood pressure (SBP) = 145 20, mean diastolic blood pressure
W.J. Cash et al. / Advances in Medical Sciences 59 (2014) 2833 29
(DBP) = 87 10 and mean BMI = 29 6) None of the patients were
smokers.
3.2. Clinical evaluation
A signicant reduction in mean SBP was identied at nine
months following venesection (Baseline: 145 20 mm Hg vs. 9
months: 131 22 mm Hg, p = 0.02), However, SBP at study comple-
tion remained unchanged from baseline. Mean DBP were unaffected
by venesection (Table 1). No signicant change in BMI was noted
(Baseline: 29 6 vs. 12 months: 30 5, p = 0.80).
3.3. Haematological and biochemical assessment
Fasting glucose levels were not affected by venesection (Baseline:
5.7 1.4 mmol/L vs. 12 months: 5.5 1.1 mmol/L, p = 0.89). Although
venesection had a positive impact on high density lipoprotein (HDL)
(Baseline: 1.3 0.3 mmol/L vs. 12 months: 1.4 0.3 mmol/L, p = 0.01),
there was no signicant effect on total cholesterol, low density
lipoprotein (LDL) or triglyceride levels (Table 1).
Vensection had a positive effect on liver biochemistry with
signicant reductions in alanine transaminase (ALT) identied as
early as six weeks (Baseline: 64 46 U/L vs. 6 weeks: 50 34 U/L,
p = 0.01) and continued improvements at twelve months in ALT
(Baseline: 64 46 U/L vs. 12 months: 30 15 U/L, p = 0.001) and
aspartate transaminase (AST) (Baseline: 47 24 U/L vs. 12 months:
30 11 U/L, p = 0.05) (Table 1).
Ferritin (Baseline: 1161 657 ng/ml vs. 12 months:
159 328 ng/ml, p < 0.001) and transferrin saturation (Baseline:
85 20% vs. 43 25%, p = 0.005) were signicantly reduced after
twelve months of venesection compared to baseline. While total iron
binding capacity (TIBC) (Baseline: 43 5 mg/L vs. 12 months:
54 8 mg/L, p = 0.002) signicantly increased compared to baseline.
Whilst there was a reduction in serum iron levels, it was not
statistically signicant (Baseline: 37 11 mmol/L vs. 12 months:
22 11 mmol/L, p = 0.14) (Table 1).
3.4. Endothelial function
3.4.1. Lipid hydroperoxides
There was no signicant difference in lipid hypoperoxides over
the study period (Baseline: 0.6 0.1 mmol/L vs. 12 months:
0.5 0.1 mmol/L, p = 0.45) (Table 1).
Table 1
Analysis of clinical and haematological parameters, serological endothelial function, anti-oxidant status, high sensitive C-reactive protein and vascular compliance using the
Friedman test. Results are presented as mean and standard deviations.
Assessment time-point
Parameter Baseline 6 weeks 3 months 6 months 9 months 12 months p-Value
SBP (mm Hg) 145.40 (19.87) 141.20 (18.75) 138.20 (19.93) 137.00 (18.08) 131.40 (29.08) 146.20 (22.01) 0.08
DBP (mm Hg) 87.20 (10.18) 84.00 (10.11) 85.60 (6.80) 83.65 (6.89) 81.90 (8.71) 87.90 (11.72) 0.39
Glucose (mmol/L) 5.67 (1.36) 5.78 (0.95) 5.42 (1.14) 5.37 (1.23) 5.53 (1.01) 5.47 (1.06) 0.89
Cholesterol (mmol/L) 4.61 (1.14) 4.49 (0.98) 4.66 (0.88) 4.71 (0.93) 4.75 (1.02) 4.82 (1.00) 0.66
HDL (mmol/L) 1.25 (0.27) 1.30 (0.32) 1.32 (0.31) 1.40 (0.32) 1.37 (0.33) 1.37 (0.34) 0.01
LDL (mmol/L) 2.59 (1.00) 2.41 (0.95) 2.48 (0.79) 2.60 (0.98) 2.64 (0.87) 2.69 (1.08) 0.95
HDL/LDL Ratio 3.82 (1.19) 3.65 (1.20) 3.73 (1.25) 3.51 (1.05) 3.63 (1.08) 3.78 (1.45) 0.36
Triglycerides (mmol/L) 1.72 (1.01) 1.75 (1.34) 1.91 (1.28) 1.56 (0.98) 1.64 (1.03) 1.68 (0.81) 0.78
Iron (mmol/L) 36.60 (10.05) 32.90 (12.07) 31.20 (17.22) 31.20 (17.70) 24.15 (14.47) 22.30 (11.42) 0.14
Ferritin (ng/ml) 1161.30 (656.74) 844.60 (899.27) 570.60 (497.46) 356.40 (389.42) 433.35 (1002.51) 158.50 (328.35) <0.001
Transferrin saturation (%) 85.37 (19.88) 75.32 (23.36) 66.74 (30.56) 62.44 (31.89) 48.05 (28.85) 42.60 (25.44) 0.005
TIBC (mg/L) 43.00 (5.42) 43.50 (6.08) 45.00 (8.84) 48.60 (10.19) 50.60 (5.76) 54.10 (7.87) 0.002
Bilirubin (mmol/L) 13.70 (6.45) 11.50 (4.48) 10.65 (7.39) 11.10 (4.53) 11.10 (3.41) 12.30 (4.81) 0.09
Albumin (g/L) 45.80 (3.01) 45.10 (1.52) 46.15 (3.45) 46.60 (0.97) 46.30 (1.70) 45.30 (3.47) 0.15
ALP (U/L) 79.20 (20.12) 77.80 (17.18) 75.40 (17.99) 74.50 (19.74) 84.10 (41.68) 86.30 (32.67) 0.49
ALT (U/L) 63.90 (45.52) 49.90 (34.41) 41.00 (26.67) 31.00 (10.03) 48.80 (69.34) 30.00 (15.00) 0.001
AST (U/L) 46.80 (24.09) 41.50 (20.71) 38.30 (19.86) 32.50 (8.64) 42.10 (42.80) 30.30 (10.80) 0.05
gGT (U/L) 98.50 (104.49) 74.50 (84.43) 75.70 (88.75) 75.55 (84.95) 146.90 (258.88) 65.10 (75.38) 0.09
HPO (mmol/L) 0.57 (0.14) 0.55 (0.17) 0.53 (0.22) 0.51 (0.16) 0.47 (0.09) 0.51 (0.09) 0.45
sICAM1 (ng/ml) 427.40 (182.61) 313.90 (119.46) 395.60 (174.11) 399.05 (238.72) 361.00 (108.27) 307.22 (122.12) 0.54
sVCAM1 (ng/ml) 517.70 (192.87) 407.00 (148.24) 534.40 (257.70) 525.90 (288.96) 488.40 (187.01) 377.50 (119.79) 0.51
Vitamin C (mmol/L) 67.46 (34.91) 66.35 (36.01) 66.38 (44.95) 76.39 (59.03) 83.42 (43.10) 77.76 (52.21) 0.95
a-Carotene (mmol/L) 0.07 (0.05) 0.06 (0.03) 0.04 (0.03) 0.05 (0.04) 0.06 (0.06) 0.06 (0.05) 0.94
a-Tocopherol (mmol/L) 26.15 (6.46) 25.82 (6.83) 25.65 (6.28) 24.45 (4.37) 25.84 (7.63) 25.62 (6.63) 0.94
b-Carotene (mmol/L) 0.23 (0.12) 0.21 (0.10) 0.21 (0.18) 0.21 (0.15) 0.23 (0.16) 0.25 (0.19) 0.97
b-Cryptoxanthin (mmol/L) 0.06 (0.04) 0.06 (0.04) 0.06 (0.05) 0.07 (0.07) 0.07 (0.06) 0.06 (0.04) 0.56
g-Tocopherol (mmol/L) 2.92 (1.06) 3.11 (1.46) 3.02 (1.17) 2.72 (1.02) 2.85 (1.15) 2.55 (1.29) 0.51
Lutein (mmol/L) 0.12 (0.04) 0.10 (0.03) 0.11 (0.05) 0.10 (0.04) 0.11 (0.03) 0.10 (0.05) 0.88
Lycopene (mmol/L) 0.53 (0.35) 0.43 (0.24) 0.36 (0.20) 0.61 (0.55) 0.57 (0.41) 0.74 (0.68) 0.23
Retinol (mmol/L) 1.66 (0.75) 1.66 (0.69) 1.34 (0.79) 1.30 (0.64) 1.81 (0.84) 1.56 (0.47) 0.22
Zeaxanthin (mmol/L) 0.03 (0.01) 0.02 (0.01) 0.03 (0.03) 0.03 (0.02) 0.03 (0.02) 0.03 (0.02) 0.82
hsCRP (mg/dL) 290.75 (263.94) 232.27 (199.07) 258.42 (197.43) 344.47 (620.98) 536.44 (1050.35) 224.26 (170.30) 0.25
AgIx75 (%) 19.77 (11.63) 17.43 (11.99) 15.58 (15.20) 17.55 (13.38) 19.08 (11.83) 16.37 (14.08) 0.22
TR (msec) 145.60 (12.05) 145.48 (8.92) 146.77 (13.45) 143.47 (14.04) 145.33 (16.02) 142.65 (6.48) 0.95
ED (%) 35.72 (3.23) 36.35 (5.09) 35.42 (3.41) 33.57 (3.51) 35.05 (4.21) 37.02 (5.57) 0.28
SEVR (%) 153.38 (16.22) 150.88 (27.70) 159.58 (21.34) 170.93 (24.52) 159.68 (22.33) 147.38 (28.64) 0.21
PWV (m/s) 9.65 (2.35) 9.03 (2.69) 8.85 (1.40) 9.00 (1.17) 9.22 (0.96) 8.74 (1.16) 0.34
ALP, alkaline phosphatase; ALT, alanine aminotransferase; AST, aspartate transaminase; DBP, diastolic blood pressure; GGT, g-glutamyl transpeptidase; HDL, high density
lipoprotein; LDL, low density lipoprotein; SBP, systolic blood pressure; TIBC, total iron binding concentration, hsCRP, high sensitive C-reactive protein; HPO, hydroperoxides;
sICAM1, soluble intracellular adhesion molecule-1; sVCAM1, soluble vascular cell adhesion molecule-1, AgIx75, augmentation index calibrated to 75 beats per minute; ED,
ejection duration; PWV, pulse wave velocity; SEVR, subendocardial viability ratio; TR, time to reectance.
W.J. Cash et al. / Advances in Medical Sciences 59 (2014) 2833 30
3.4.2. Cell adhesion molecules
There was no signicant change in sICAM (Baseline:
427 183 ng/ml vs. 12 months: 307 122 ng/ml, p = 0.54) and
sVCAM (Baseline: 518 193 ng/ml vs. 12 months: 378 120 ng/ml,
p = 0.51) (Table 1).
3.5. Antioxidant status
There was no signicant alteration in anti-oxidant status over
the 12 month study period. Vitamin C (Baseline: 68 35 mmol/L vs.
12 months: 78 52 mmol/L, p = 0.95), b-carotene (Baseline: 0.2
0.1 mmol/L vs. 12 months: 0.3 0.2 mmol/L, p = 0.97) and lycopene
levels (Baseline: 0.5 0.4 mmol/L vs. 12 months: 0.7 0.7 mmol/L,
p = 0.23) were not signicantly increased from baseline (Table 1).
3.6. High sensitive C-reactive protein
There was no signicant change in hsCRP levels at twelve
months (Baseline: 291 264 mg/dL vs. 12 months: 224 170 mg/
dL, p = 0.25) (Table 1).
3.7. Vascular compliance
Venesection did not signicantly alter PWV (Baseline:
10 2 m/s vs. 12 months: 9 1 m/s, p = 0.34), AgIx75 (Baseline:
19.8 11.6% vs. 12 months: 16.4 14.1%, p = 0.22), SEVR (Baseline:
153 16% vs. 12 months: 147 29%, p = 0.21) and TR (146 12 ms
vs. 143 7 ms, p = 0.95) (Table 1).
4. Discussion
Increased cardiovascular risk has previously been linked to an
elevation in body iron stores particularly from research performed in
the Finnish population who are known to have a high incidence of
HFE haemochromatosis [1218]. It has also been suggested that
elevated ferritin levels identied in HFE haemochromatosis can lead
to iron deposition and cardiovascular complications [1921]. In
addition, Ellervik et al. [22] have recently reported the association of
the HFE C282Y haemochromatosis genotype, elevated transferrin
saturation and an increased risk of antihypertensive use.
The strongest arguments against this association have come
from a large individual patient meta-analysis by van der A et al.
[23] that excluded increased cardiovascular risk in individuals
heterozygous for haemochromatosis and an autopsy study by
Miller et al. [24] that suggested a degree of cardioprotection in
those with hemochromatosis associated with HFE C282Y homo-
zygosity. The latter has recently been explained by mutational
effect of selective iron depletion of the macrophage, a key cell type
in atherogenesis [25,26].
It is currently unclear if venesection reduces cardiovascular
risk. Zacharski et al. [27,28] acknowledged a possible trend
towards improved outcomes particularly in younger patients
when assessing the effects of six-monthly venesection on
cardiovascular outcomes in symptomatic peripheral vascular
disease. However, they reported no signicant decrease in all-
cause mortality, myocardial infarction and stroke.
Whilst the potential mechanism for advantageous haemody-
namic effects remains unclear following venesection, some postu-
late that observed differences may reect the enhanced effect of HDL
on vascular endothelium via reduced LDL oxidation or through
cholesterol reabsorption [29]. Others have reported a relationship
between excess iron level, lipid homeostasis and cardiovascular risk.
Van Jaarsveld and Pool [30] demonstrated a 7% higher HDL level in
healthy individuals following blood donation whilst Sultana et al.
[31] identied a positive correlation between total iron binding
capacity and HDL levels in patients who suffered acute myocardial
infarction. This improvement in HDL levels could have signicant
clinical implications particularly as Rubins et al. [32] revealed that a
7.5% increase in HDL resulted in a 22% reduction in coronary events
in males with known cardiovascular disease.
Our study identied that iron reduction in HFE haemochroma-
tosis was associated with a signicant 9.6% rise in HDL. However, it
did not otherwise affect the lipid prole and targeting HDL level
alone does not appear to be benecial in reducing cardiovascular
risk. In a recent trial of patients who had had a recent acute coronary
syndrome, treatment with dalcetrapib markedly increased HDL
cholesterol levels (3140%) compared to placebo (411%) but didnot
reduce LDL cholesterol level or the risk of recurrent cardiovascular
events [33]. Despite this result, new research has suggested that
importance of HDL particle number in cardiovascular outcome and
highlights that manipulation of HDL may still have important
clinical applications in this setting [34,35].
Given the positive changes in HDL with vensection, it was
postulated that further advantageous effects may include improve-
ments in endothelial function, anti-oxidant status and vascular
compliance. However, contrary to some published evidence, no
signicant effect on these parameters was observed in this study.
Gaenzer et al. [18] previously found a correlation between iron and
thiobarbituric acid-reactive substance (TBARS). Although TBARS is a
less specic assessment of lipid peroxidation than the FOX 1 assay,
their TBARS results were supported by measurement of glutathione
levels and suggest that oxidative stress was at least indirectly related
to iron [36]. Furthermore Houglum et al. [37] identied higher
oxidatively modied proteins (carbonyl groups) in untreated HFE
haemochromatosis patients compared to controls (110 nmol/mL vs.
53 nmol/mL, p < 0001), which following venesection decreased
signicantly compared to untreated HFE C282Y haemochromatosis
patients (66 nmol/mL vs. 110 nmol/mL, p < 0001).
Shizukuda et al. [38] measured oxidative stress-related bio-
chemical markers in three asymptomatic age- and gender-matched
groups including newly diagnosed HFE haemochromatosis patients
(n = 22), HFE haemochromatosis subjects who had undergone at
least six months of venesection (n = 21) and controls (n = 21). Newly
diagnosed HFE haemochromatosis patients had a signicant decline
in markers of oxidative stress (erythrocyte glutathione: 6.8 mmol/
gHb vs. 4.1 mmol/gHb, p < 0.001; plasma myeloperoxidase: 27.3 ng/
ml vs. 14.3 ng/ml, p < 0.05) following the completion of six months
of venesection therapy. However, HFE C282Y haemochromatosis
patients with more than six months of previous venesection
demonstrated signicant elevations in oxidative stress markers
compared with controls (erythrocyte glutathione: 8.3 mmol/gHb vs.
3.6 mmol/gHb, p < 0.05; plasma lipid peroxidation: 3.5 ng/ml vs.
2.0 ng/ml, p < 0.05; plasma myeloperoxidase: 69.8 ng/ml vs. 4.6 ng/
ml, p < 0.05). Their data may suggest that initial, intensive
phlebotomy therapy attenuates oxidative stress in HFE haemochro-
matosis subjects but that oxidative stress may persist or rebound
during the maintenance phase of venesection. In the same cohort the
authors found that venesection did not improve left ventricular
systolic function as determined by exercise echocardiography and
electrocardiography but strain rate, a sensitive echocardiography
derived measure of diastolic function, did appear to correlate with
the above biomarkers of oxidative stress [39,40].
Previous research from our own group has demonstrated that at
various stages of treatment, HFE haemochromatosis patients when
compared to healthy controls have signicantly diminished levels of
Vitamin C (51.3 mmol/L vs. 89.1 mmol/L, p = 0.013), retinol
(1.78 mmol/L vs. 2.46 mmol/L, p = 0.001) and alpha-tocopherol
(5.91 mmol/L vs. 7.24 mmol/L, p = 0.001).[6] Assessment of patients
attending a HFE haemochromatosis venesection programme in this
current study afforded an opportunity to determine the effects of
treatment over a period of time rather than at a solitary time-point as
reported in our previous study and found no change in anti-oxidant
W.J. Cash et al. / Advances in Medical Sciences 59 (2014) 2833 31
status [6]. Previous literature regarding venesection in patients with
iron overload as described by Brissot et al. [41] has shown an
increase in Vitamin C in 67 venesection treated HFE haemochro-
matosis patients (untreated: 19.5 mg/10
8
WBC vs. treated 34.3 mg/
10
8
WBC). Despite published evidencesupporting increased levels of
vitamin C following venesection in iron overload, van Jaarsveld and
Pool [30] discovered a signicant reduction in vitamin C levels when
23 healthy males donated 500 ml of blood on three occasions within
six weeks (28.58 mM vs. 8.59 mM, p = 0.0347). Therefore if
venesection is associated with improvement in anti-oxidant status
it may be limited to individuals with iron overload.
Endothelial dysfunction has long been recognised as an
important early functional abnormality and accepted surrogate
marker of atherosclerosis while hsCRP is a predictor of cardiovas-
cular events and mortality [4245]. Such reductions in vascular
compliance detected by elevated PWV combined with associated
serological endothelial dysfunction suggest increased cardiovas-
cular risk [46]. Kiechl et al. [14] previously suggested an
association between serum ferritin concentrations and progression
of carotid atherosclerosis in the general population. More recently
Gaenzer et al. [18] reported a relationship between endothelial
dysfunction, detected by a reduction in endothelium-dependent
dilation (EDD) of the brachial artery, and increased intima-media
thickness (IMT) of the carotid artery when male HFE haemochro-
matosis patients receiving venesection were compared with age-
matched controls. They also identied that when previously
untreated male HFE haemochromatosis patients were re-investi-
gated after venesection, a signicant improvement in EDD was
observed (2.6% vs. 5.5%, p = 0.0015).
In keeping with a non-signicant change in arterial compliance
in our study, others suggest the absence of any relationship
between serum iron and vascular compliance. Vergnaud et al. [47]
reported that there was no association between baseline serum
ferritin levels, iron intake levels at baseline and subsequent PWV
after 7.5 years of follow-up. They also reported no relationship
between iron proles, carotid artery IMT or presence of carotid
plaques. The majority of other studies in the general population
concur with the absence of such a relationship [14,4851]. On the
other hand, it is important to note that Vergnaud et al. [47]
excluded patients with HFE C282Y haemochromatosis and our
study is only the second study that has assessed vascular
compliance specically in HFE haemochromatosis.
Given that previous researchers have described a relationship
between body iron stores, endothelial dysfunction and overall
cardiovascular risk it is suggested that further larger prospective
studies to evaluate the impact of venesection on serological
endothelial dysfunction, antioxidant status and vascular compli-
ance in HFE haemochromatosis patients are required [1218].
5. Conclusions
Vensection is in HFE haemochromatosis correlates with an early
and sustained improvement in HDL. Such an improvement does
not appear to be related to signicant improvements in serological
endothelial function, antioxidant status and arterial compliance.
However, larger studies using this established methodology are
required to clarify this relationship further.
Conict of interests
None.
Financial disclosure
The authors greatly acknowledge the nancial support of The
Royal Victoria Hospital Liver Support Group.
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