Clinical Trial Details
— Status: Recruiting
Administrative data
| NCT number |
NCT00190073 |
| Other study ID # |
FEMH-94003 |
| Secondary ID |
FEMH-94003 |
| Status |
Recruiting |
| Phase |
N/A
|
| First received |
September 11, 2005 |
| Last updated |
September 11, 2005 |
| Start date |
January 2005 |
| Est. completion date |
December 2005 |
Study information
| Verified date |
September 2005 |
| Source |
Far Eastern Memorial Hospital |
| Contact |
Ming-Tsung Tseng, MD |
| Phone |
886-2-89667000 |
| Email |
mingtsungtseng[@]yahoo.com.tw |
| Is FDA regulated |
No |
| Health authority |
Taiwan: Department of Health |
| Study type |
Observational
|
Clinical Trial Summary
Peripheral neuropathy is a frequent neurological complication of chronic alcoholism. Most
studies evaluated large-fiber involvement by nerve conduction studies (NCS). Since previous
studies document the predominant injury of small myelinated and unmyelinated fibers in
patients with alcoholic neuropathy, it will be imperative to know their prevalence and
clinical significance. Moreover, the pathogenesis of alcoholic neuropathy, especially the
roles of ethanol and its metabolites and thiamine, remains elusive. This proposal will be
designed to understand the extent and clinical significance of cutaneous nerve degeneration
in the skin of alcoholic patients and to investigate its pathogenesis. We will investigate
cutaneous innervation by 3 mm punch skin biopsies with immunohistochemistry for protein gene
product 9.5 and quantifying epidermal nerve density (END) in alcoholic patients. Patients
will undergo clinical evaluation, quantitative sensory testing (QST), nerve conduction
studies (NCS), and tests of sympathetic skin response (SSR) and beat-to-beat RR interval
variability (RRIV). The prevalence of peripheral neuropathy in chronic alcoholic patients
with emphasis on small-fiber involvement will be first evaluated. The sensitivity of punch
skin biopsy, QST, SSR and RRIV tests, and NCS will be compared, and the correlations between
END and psychophysic and electrodiagnostic parameters will be discussed. Subsequently, we
will elucidate the clinical significance of END reduction in alcoholic patients. Patients
with evidences of involvement of central nervous system will be excluded, and END will be
correlated with clinical manifestations and neurological deficits. Finally, the role of
ethanol and thiamine in alcoholic neuropathy will be further studied. To clarify the role of
thiamine in alcoholic neuropathy, we will examine whether it has influences on small-fiber
degeneration. This may provide important information in understanding the pathogenesis and
designing optimal treatment for alcoholic neuropathy.
Description:
Alcoholic patients and control subjects. Alcoholic patients will be recruited from
neurologic clinics and ward at the Far Eastern Memorial Hospital, Taipei, Taiwan. A detailed
clinical history that includes daily alcohol consumption, daily dietary intake, lifestyle,
and occupation will be obtained from patients as well as their families. The inclusion
criteria include daily uptake of at least 100 g ethanol for more than 3 years prior to the
onset of neuropathic symptoms (Behse and Buchthal, 1977). All patients will undergo clinical
and neurologic assessment, cranial MRI or CT, and neuropsychological evaluation to rule out
CNS disorders, which interfere the evaluation of neuropathic symptoms and signs and
psychophysic test. Laboratory investigations will include complete blood count, fasting
plasma glucose, hemoglobin A1C, liver and renal function tests, ethanol level, tumor
markers, antinuclear antibodies, complement factors, serum protein electrophoresis, thyroid
function, human immunodeficiency virus, hepatitis virus, and vitamin B12 level. Thiamine
status will be assessed at the time of the first referral to the hospital by measuring total
thiamine concentration in whole blood by high performance liquid chromatography, as
described elsewhere (Koike et al., 2001 and 2003). None of the patients will administrate
thiamine at the time of determination. Age- and gender-matched control subjects will be
retrieved from our database, who will be evaluated by detailed questionnaires and
neurological examinations to exclude any neurological disorder or clinical neuropathy
(McCarthy et al., 1995).
Skin biopsy. Skin biopsy will be performed following established procedures after informed
consent has been obtained (McCarthy et al., 1995; Pan et al., 2003; Shun et al., 2004).
Under local anesthesia with 2% lidocaine, punches 3mm in diameter will be taken from the
following locations: (1) the extensor side of the distal forearm, 5 cm above the middle
point of a line connecting the radial styloid process and the ulnar styloid process; and (2)
the lateral side of the distal leg, 10 cm above the lateral malleolus. No suturing will be
required, and the wounds will be covered with a piece of gauze. Wound healing takes 7–10
days, the same as would a typical abrasion wound. The protocol is under review by the Ethics
Committee of Far Eastern Memorial Hospital.
Immunohistochemistry. For immunohistochemistry on freezing microtome sections, the skin
samples will be fixed with 4% paraformaldehyde in 0.1M phosphate-buffered saline (PBS), pH
7.4, for 48 h (McCarthy et al., 1995; Hsieh et al., 2000). Sections of 50 mm perpendicular
to the dermis will be cut on a sliding microtome (model 440E; Microm, Walldorf, Germany).
They will be quenched with 1% H2O2, blocked with 5% normal goat serum, and incubated with
rabbit antiserum to PGP 9.5 (UltraClone, UK, diluted 1: 1000 in 1% normal serum/Tris) at 4C
for 16–24 h. After rinsing in Tris, sections will be incubated with biotinylated goat
anti-rabbit IgG at room temperature for 1 h, followed by incubation with avidin–biotin
complex (Vector, Burlingame, CA) for another hour. The reaction product will be demonstrated
with chromogen SG (Vector, Burlingame, CA), and counterstained with eosin (Sigma, St. Louis,
MO).
Quantitation of epidermal innervation. Epidermal innervation will be quantified following
established protocols, and slides will be coded to ensure that measurements are blinded
(Hsieh et al., 2000; Pan et al., 2003; Shun et al., 2004). PGP 9.5-immunoreactive nerve
fibers in the epidermis of each section will be counted at a magnification of 40 with an
Olympus BX40 microscope (Tokyo, Japan) through the depth of the entire section. Each
individual nerve with branching points inside the epidermis will be counted as one. For
epidermal nerves with branching points in the dermis, each individual nerve will be counted
separately. The length of the epidermis along the upper margin of the stratum corneum in
each section will be measured using Image-Pro PLUS (Media Cybernetics, Silver Spring, MD).
END will therefore be derived and expressed as fibers/mm. For each tissue, there will be
48–50 sections, and all sections will be sequentially labeled. Every fifth section will be
immunostained and quantified. The mean of values from these sections will be considered the
END of the tissue specimen. In the distal leg, normative values from our laboratory (mean
SD, 5th percentile) of END are 11.16 3.70, 5.88 fibres/mm for subjects aged < 60 years and
7.64 3.08, 2.50 fibres/mm for subjects aged 60 years. The cut-off point of END is 5.88
and 2.50 fibres/mm in the two age groups, respectively.
Quantitative sensory testing. We will perform quantitative sensory testing (QST) with a
Thermal Sensory Analyzer and Vibratory Sensory Analyzer (Medoc Advanced Medical System,
Minneapolis, MN) to measure thresholds of warm, cold, and vibratory sensations following the
established protocol (Pan et al., 2001; Pan et al., 2003; Yarnitsky and Ochoa, 1991).
Briefly, the machine will deliver a stimulus of constant intensity which had been determined
by the test algorithm. The intensity of the next stimulus will be either increased or
decreased by a fixed ratio according to the response of the subject, i.e., whether or not
the subject perceives the stimulus. Such procedures will be repeated until a pre-determined
difference of intensity is reached. The mean intensity of the last two stimuli will be the
threshold for the level method. Thermal thresholds recorded on the toe will be expressed as
warm threshold temperature and cold threshold temperature, respectively. These temperatures
will be compared with normative values (Pan et al., 2003). Vibratory thresholds recorded on
the malleolus will be measured with similar algorithms. Normative values are documented
previously and are similar to those of previous reports (Pan et al., 2001; Pan et al.,
2003). Threshold values greater than the 95th percentile value for each age group will be
considered abnormal.
Nerve conduction studies. NCS will be carried out in all patients with a Keypoint
electromyographer following standardized methods (Pan et al., 2003). Amplitudes of compound
muscle action potential (CMAP) and sensory action potential (SAP) will be analyzed according
to the normative data in our laboratory. Studied nerves include bilateral median, ulnar,
peroneal, tibial, and sural nerves. Abnormal result on NCS is defined as having
abnormalities of 1 or more nerves with reduced amplitude, prolonged distal latency, or
slowed nerve conduction velocity. Neurophysiologic criteria of sensorimotor polyneuropathy
are defined as having symmetrical abnormalities in motor and sensory nerves (Dyck et al.,
1985).
Tests of the autonomic nervous system. Sudomotor function will be examined using the
sympathetic skin response (SSR) (Ravits, 1997). Results of SSR in the palm and sole will be
interpreted as present or absent, but will not be evaluated quantitatively because of
variations in the latencies and amplitudes of SSR. Parasympathetic function will be
evaluated using the beat-to-beat heart rate variation [RR interval variability (RRIV)] at
rest and during deep breathing (Ravits, 1997). Each test will be performed three times, and
the mean value will be compared with that for the age-matched controls in our laboratory.
Medication that interferes with sympathetic or parasympathetic functions will not be
administered before or during these tests.
Statistical analysis. Numerical variables following Gaussian distribution will be compared
using t-test and expressed as the mean SD; for those variables not following Gaussian
distribution, data will be expressed as the median (range) and will be analyzed with
non-parametric Mann-Whitney U test. Results are considered significant if p < 0.05.
Patients with evidences of CNS disorders will be excluded first. Furthermore, those with
attributable etiologies for neuropathy, such as diabetes, uremia, autoimmune disorders, or
neoplasm will be excluded, too. The rest alcoholic patients will be separated as 2 groups:
alcoholic patients with normal thiamine level (ATN) and alcoholic patients with thiamine
deficiency (ATD). In the ATN group, patients will be further subgrouped as alcoholic
patients without clinical evidence of neuropathy, alcoholic patients with sensory symptoms
(especially burning lightning pains and painful paresthesia), and alcoholic patients with
sensory and motor symptoms.
The first point to address in our study is to evaluate the prevalence of peripheral
neuropathy in chronic alcoholic patients with emphasis on small-fiber involvement. Since
early detection of neural degeneration is important, the sensitivity of punch skin biopsy,
QST, NCS, and SSR and RRIV tests will be compared. The correlations between END and
psychophysic and electrodiagnostic parameters will be discussed.
Second, we will elucidate the clinical significance of END reduction in alcoholic patients.
END will be correlated with clinical manifestations and neurological deficits. Small-fiber
sensory symptoms and signs will be correlated with END, and autonomic symptoms and signs
will be correlated with the presence of sweat gland denervation. The degrees of END
reduction in the 3 groups of ATN patients and control subjects will be compared. Since other
systemic disease, especially diabetes, also causes small-fiber degeneration, we will examine
whether alcoholic patients with diabetes have further cutaneous denervation.
Finally, the role of ethanol and thiamine in alcoholic neuropathy will be explored. The
reduction of END will be correlated with thiamine status, lifetime ethanol dose, ethanol
level, and other laboratory parameters. If END correlates with ethanol consumption, it will
support the conclusion that alcoholic neuropathy is caused by direct toxic effect of ethanol
or its metabolites. Since previous report documented the large-fiber-predominant axonal loss
in sural nerve specimens in patients with pure-form of thiamine-deficiency neuropathy (Koike
et al., 2003), we wonder if thiamine level influences small-fiber degeneration, i.e.,
reduction of END. The degrees of END reduction between alcoholic patients with ATD and those
with ATN will be compared. These will further clarify the role of thiamine in alcoholic
neuropathy.
