Objectives: Hepatitis C virus (HCV) infection is often associated with cryoglobulinaemia (CG). Peripheral neuropathy (PN) is a comparatively common complication of CG associated with HCV infection and it is thought to be attributable to nerve ischaemia. Only few HCV CG patients with PN have been reported. The recent finding of HCV RNA in nerve biopsy specimens has suggested a possible direct role of HCV in the pathogenesis of PN. The authors studied 51 HCV patients to determine the prevalence of CG and to clarify the possible mechanism by which HCV determines the PN.
Methods: All the patients were studied clinically, by laboratory tests and electrophysiologically. Twenty eight patients underwent sural nerve biopsy where both morphological and morphometric evaluation of the biopsy specimen was performed, as well as statistical analysis.
Results: CG was found in 40 of 51 cases (78%). Polyneuropathy was significantly prevalent in CG+ patients compared with CG− (18 of 40 compared with 1 of 11 patients; p=0.01). HCV CG− patients more frequently developed well defined mononeuropathy or multiple neuropathy when compared with HCV CG+ (10 of 11 compared with 22 of 40; p<0.03). HCV CG+ patients showed significantly higher proportion of rheumatoid factor positivity (p<0.001) and low C4 levels (p=0.001). Nerve biopsy was performed in 25 of 40 HCV CG+ patients and in 3 of 11 HCV CG− patients: epineurial vasculitis was present in 8 of 25 HCV CG+ (32%) and in 2 of 3 HCV CG−. Differential fascicular loss of axons was found in 10 of 25 CG+ (40%) and 1 of 3 CG−, signs of both demyelination and axonal degeneration were present in 7 of 25 CG+ (28%). No significant difference was found in neuropathological features, while histometrical analysis disclosed more severe involvement in CG+ patients.
Conclusions: These findings suggest that the presence of CG is a negative predictive factor for the associated PN. Morphological findings in the sural nerve from HCV CG− and CG+ are consistent with an ischaemic mechanism of nerve damage and are against a direct role of the virus in causing the associated PN.
- hepatitis C virus
- CG, cryoglobulinaemia
- HCV, hepatitis C virus
- PN, polyneuropathy
- SCV, sensory conduction velocity
- SAV, sensory action potential
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- CG, cryoglobulinaemia
- HCV, hepatitis C virus
- PN, polyneuropathy
- SCV, sensory conduction velocity
- SAV, sensory action potential
Cryoglobulinaemia (CG) is a condition characterised by the presence of serum proteins that reversibly precipitate in the cold. According to the molecular composition, cryoglobulins are classified into three types: type I, isolated monoclonal Ig; type II, monoclonal IgM rheumatoid factor (RF) associated with a polyclonal component; type III, polyclonal Ig.1 Types II and III are classically referred to as “mixed cryoglobulinaemia”.
CG may be idiopathic (essential mixed cryoglobulinaemia, EMC) or secondary to other diseases, such as lymphoproliferative disorders, collagen diseases, and chronic infections. It has been reported that 46%–54% of patients with chronic hepatitis C virus (HCV) infection show detectable CG, although most of them do not have CG related symptoms.2,3
According to different reports, peripheral neuropathy (PN) is present in variable proportions in patients with symptomatic CG, related or not to HCV.4–8 PN usually occurs in type II and type III CG, rather than type I, and may clinically present as a mononeuropathy, multiple mononeuropathy, or polyneuropathy. Nerve biopsy shows mainly axonal degeneration.9–12 Two main pathogenetic mechanisms have been suggested: interference of the vasa nervorum microcirculation by intravascular deposits of cryoglobulins and vasculitis induced ischaemia.11,13,14 A third mechanism, an immunologically mediated demyelination,15 was seldom reported and has not been supported by subsequent studies.
Recently some HCV+ patients with PN and persistent negativity for CG have been reported.16,17 It has also been reported the finding of HCV RNA in homogenates of nerve biopsy specimens in five patients by in situ RT-PCR.18 These studies suggested a possible direct role of HCV in the pathogenesis of PN.
We examined a series of 51 consecutive HCV neuropathic patients to assess the prevalence of CG and to clarify the pathogenetic mechanism by which HCV determines PN.
We examined 51 consecutive patients with HCV infection and neuropathy, referred to our department in the past eight years. Other causes of PN, except for the presence of monoclonal gammopathy, were excluded (diabetes, alcohol misuse, renal failure, vitamins deficiency, thyroid disorder, neoplasm, toxicity). The patients were all studied clinically, serologically, and electrophysiologically; 28 patients accepted to undergo nerve biopsy. The time lapse of the follow up was of four years or longer; all the patients at the time of the study were untreated. Peripheral nerve involvement was classified as mononeuropathy and/or multiple neuropathy, cranial neuropathy, and polyneuropathy.
All the patients had serum anti-HCV antibodies detected by enzyme linked immunosorbent assay, confirmed by the more specific recombinant immunoblot assay. Laboratory studies included routine blood tests, immunological tests (latex test for IgM rheumatoid factor, C4 values, autoantobodies), detection and characterisation of cryoglobulins according to Brouet et al.1 Cryoglobulin determinations were performed at least three times during observation.
Electrodiagnostic tests were performed with standard electromyographic equipment (Medelec MS20 Mystro); all nerve conduction studies were carried out at a constant cutaneous temperature of 33°C under automatic control with a DISA type 15 H 0.2 temperature regulator system.
We studied sensory conduction of the right median and ulnar nerve and of the sural nerve of both sides in all patients. For each nerve were considered sensory conduction velocity (SCV) and sensory action potential (SAP) amplitude. Sural and ulnar SAPs were recorded antidromically at the ankle and wrist respectively, whereas SAPs of the median nerve were obtained by antidromical stimulation at wrist and elbow to determine separately wrist to finger and elbow to wrist SCV. Computer averaging was used to determine the size of low amplitude sensory responses.
We also studied motor conduction of median, ulnar and deep peroneal nerves; for each nerve we evaluated motor conduction velocity (MCV), compound motor action potential (CMAP) amplitude and distal latency (DL). To detect changes of proximal conduction we recorded F waves (20 times for each test) from ulnar and deep peroneal nerve at the elbow and above the knee respectively: the shortest F wave latency was considered.
Muscles that underwent EMG needle examination were tibialis anterior and medial gastrocnemius. Electrophysiological parameters of the patients were considered abnormal if outside twice the standard deviation of mean values obtained from healthy age matched controls.
We studied 28 sural nerve biopsy specimens, 25 from PN CG+ and three from PN CG− patients.
The sural nerve biopsy specimens were taken just proximal to the lateral malleolus. A portion was fixed in 10% formalin, embedded in paraffin wax, and sections were stained with haematoxylin and eosin, Congo red, alcian blue, and PAS. A second portion was quickly frozen in liquid nitrogen and either frozen or paraffin wax embedded; 6 μm sections were used for direct immunocytochemical study using peroxydase conjugated goat antihuman affinity purified antibodies (IgG, IgA, IgM, 1:500 diluitions). A third portion was fixed in 2% buffered glutaraldehyde, postfixed in 1% osmium tetroxide, dehydrated, and embedded in Epon 812. Semithin transverse sections were stained with toluidine blue and examined under the light microscope to estimate the distribuition and severity of myelinated fibre abnormalities. Quantitative histometrical analysis of myelinated fibres were obtained from micrographs, at a magnification of ×1000 of three fascicles for each patient. Fifty teased myelinated fibres were studied in each patient.
The sections were analysed for the presence of signs of axonal degenerations or demyelination. Particular attention was focused on the presence of perivascular and interstitial inflammatory infiltrates; other vascular abnormalities, such as hyperplasia of muscular and endothelial cell layers, were noted. Epineurial vasculitis was diagnosed according to the criteria of Dyck et al19 when intramural infiltration with necrosis of the vessel walls was present.
Statistical analysis of the results were performed using a χ2 test (associated to Yates’s correction when necessary) and Student’s t test for unpaired data. p Values <0.01 and <0.05 were considered significant.
Fifty one HCV infected patients, 25 men and 26 women, were studied. Table 1 summarises their clinical, laboratory, and neuropathological features. Their ages at time of diagnosis ranged from 39 to 81 years; mean (SD) age 62 (10). Detectable cryoglobulins (with a cryocrit greater than 0.1%) were found in the serum in 40 of 51 patients (78%). Cryoglobulins were type III and type II. No patient had type I cryoglobulins.
Clinical examination disclosed four different patterns of peripheral nerve involvement: PN, mononeuropathy and/or multiple neuropathy (MN), cranial neuropathy (CN), polyneuropathy combined with cranial neuropathy (PN+CN). PN was a symmetrical sensorymotor neuropathy with predominant sensory features in some cases. Subgroups of multiple mononeuropathy and cranial neuropathy as well as cranial neuropathy associated with clinical polyneuropathy, were all considered to be clinical expression of an ischaemic nerve damage as other causes of focal nerve damage were excluded by inclusion clinical criteria.
Of the 40 CG+ patients, 18 had PN (45%), 16 had MN (40%), 3 had CN (7.5%), and 3 had combined PN+CN (7.5%). Among the 11 CG− patients, the clinical features were as follows: five patients had CN (46%), four patients had MN (36%), one patient had PN (9%), and one patient had combined PN+CN (9%) (table 1).
The prevalence of PN was significantly higher in CG+ patients compared with CG− (45% versus 9%; p=0.01, χ2 test). CN was significantly higher in CG− patients (46% versus 7.5%; p=0.01, χ2 test). There was no significant difference in the proportion of mononeuropathy/ multiple neuropathy and cranial neuropathy combined to polyneuropathy.
Considering CN, MN, and CN+PN as expression of a mononeuritic process, we found a significant difference between CG+ and CG− groups (p<0.03, χ2 test): CG− patients more frequently developed a well defined mononeuritic process (10 of 11, 90%) when compared with CG+ patients (22 of 40, 55%).
CG+ patients showed significantly higher proportion with rheumatoid factor positivity (87.5% versus 18%; p>0.001, χ2 test) and lower C4 levels (92.5% versus 45.5%; p=0.001, χ2 test). Increased transaminase activities (ALT>70 U/l), as possible expression of HCV cytopathic effect, were found in 67.5% of CG+ patients compared with 45.5% of CG− patients; no significant difference was found between the two groups (χ2 test).
Table 2 gives the electrophysiological findings. Analysis of the data showed a significant difference only for one parameter: MCV of deep peroneal nerve in CG+ compared with CG− patients. The other neurophysiological parameters were suggestive of a wider and more severe involvement of peripheral nerve in CG+ patients, even if no significant differences were found.
Nerve biopsy was performed in 25 CG + patients: epineurial vasculitis (fig 1) was present in 8 of 25 cases (32%), differential fascicular loss of axons (fig 2) was found in 10 cases (40%), signs of both demyelination and axonal degeneration were present in seven cases (28%). Three of the 11 CG− patients underwent sural nerve biopsy: two patients had epineurial vasculitis and one showed a differential fascicular loss of axons. In all cases, teased fibre preparation demonstrated axonal degeneration without evidence of primary demyelination. Comparison of neuropathological features disclosed no significant difference between CG+ and CG− groups (χ2 test). Table 3 gives the histometrical data of sural nerve biopsy specimens. We found a significant fibre loss in CG+ compared with CG− patients (p<0.005, t test), as well as in percentage of large myelinated fibres (p<0.05, t test). Total number of clusters, representing regenerating fibres, was significantly increased in CG− compared with CG+ patients (p<0.005, t test).
The association between HCV infection and CG is well established. Detectable CG are present in about 50% of HCV patients although most of them do not have CG related symptoms.2,3 A sensory motor PN has been found in up to 9% of patients chronically infected with HCV20,21 and the prevalence rises up to 30% in HCV CG+ patients.7,8 Most data in the literature are concerned with neuropathy in HCV CG+ patients, whereas only few of them investigate neuropathy in HCV CG− patients.16,17 Several previous studies characterised PN involvement in HCV CG+ patients as a subacute, distal, motor sensory polyneuropathy. An asymmetrical sensory impairment has often been highlighted.7,22 Mono and multiple mononeuritis have also been frequently reported.5,23 Surveys on HCV CG− patients are few, based on small samples and lacking clinical and neuropathological data.
In our series of patients affected by HCV infection and neuropathy, CG were found in 78% of patients. Polyneuropathy was significantly prevalent in CG+ patients, whereas CG− patients showed a higher prevalence of mononeuropathy or multiple neuropathy. Also Lidove,16 in his small series, reported a high prevalence of mono or multiple neuropathy in HCV CG− patients (three of four patients). As a matter of fact, electrophysiological analysis disclosed a wider than expected peripheral nervous system involvement, also in HCV CG− patients with clinical mono or multiple neuropathy. These data seem to suggest a different degree of the same pathological mechanism of nerve damage, ranging from mild/moderate in HCV CG− patients to moderate/severe in HCV CG+ patients. Laboratory data disclosed a prevalence of RF+ and lower C4 levels in HCV CG+ as compared with HCV CG−, confirming data previously reported in the literature8,21 and indicating complement activation and consumption, caused by immunocomplex formation. On the other hand, most HCV CG− patients had RF negativity and normal C4 values, as well as the four HCV CG− patients described by Lidove.16 Nevertheless, some HCV CG− patients in our series, showed humoral signs of complement activation indicating that this process was not necessarily related to the presence of CG.
Peripheral neuropathy associated with HCV is mainly characterised by axonal damage and it is usually associated with CG. It was postulated that nerve damage is secondary to epineurial vessels changes caused by occlusion or vasculitis induced by longstanding cryoglobulin precipitation with complement fixation and RF deposition. The vasculitis or vascular occlusion causes fascicular ischaemia that results in axonal degeneration.11,13,19
It has been supposed that HCV may have a direct role in the pathogenesis of neuropathy; it could induce nerve damage by a direct cytopathic effect or by an immunomediated mechanism such as immune complex induced changes of the epineural vessels. This hypothesis seems to be supported by the finding of HCV RNA in five nerve biopsy specimens by RT-PCR in situ24 and could explain the neurological involvement in CG− patients. It has also been supposed that CG or immunocomplexes, or both, contribute to the generation of microvascular, but not vasculitic, changes in epineurial and endoneurial capillaries, whereas only T cell dependent mechanism account for the epineurial inflammation.18
We found pathological evidence of a vasculitic process both in HCV CG+ and in HCV CG− patients. In fact either epineurial vasculitis and fascicular axonal loss suggest ischaemia as a cause of the neuropathy.
Cryoglobulins are immunocomplexes able to activate the complement pathway and cause vasculitis. Regarding the pathophysiology of the vasculitic process in HCV CG− neuropathy, the activation of the complement may be attributable to three different mechanisms: an innate mechanism caused by the ability of the virus itself to activate the complement pathway, a second mechanism based on the reactivity of natural killer cells against the viral proteins, and a third mechanism supposing the existence of an interaction between HCV and anti-HCV antibodies. Thus, vasculitis might be attributable to immunocomplex deposition not related to the presence of CG in the serum. It is well established that the major HCV envelope protein inhibits natural killer cells25; nevertheless complement pathway may be activated by the reactivity of natural killer cells with HCV or by HCV/anti-HCV immunocomplex formation. To date there are no data in the literature concerning the ability of HCV to activate the innate mechanism of complement activation, even if it is well known that virus may trigger complement pathway independently of adaptive immune responses.26
In summary, our study disclosed a more severe impairment in HCV CG+ patients as compared with CG−, either by clinical, electrophysiological, and histometrical analysis. The mechanism of peripheral nerve damage seems to be vasculitic in both CG+ and CG− patients, as supported by the clinical and morphological findings. The presence of CG in the serum is predictive of a more severe and widespread neuropathic involvement, but there is evidence that cryoglobulins are not the unique factor involved in the vasculitic process. Further studies are needed to clarify the role of HCV in innate complement activation and the relevance of the “in situ” HCV induced chronic stimulation of the immune system.
Competing interests: none declared.