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Department of Gastroenterology and Hepatology, Medizinische Poliklinik, University of Würzburg, Klinikstrasse 6-8, D-97070 Würzburg, Germany
1 Division of Metabolism, Endocrinology and Molecular Medicine, Medizinische Poliklinik, University of Würzburg, Würzburg, Germany
2 Institute for Virology and Immunobiology, University of Würzburg, Versbacher Strasse 7, D-97078 Würzburg, Germany
(Requests for offprints should be addressed to M R Kraus; Email: Kraus_m{at}klinik.uni-wuerzburg.de)
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Abstract |
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Introduction |
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However, interferon alfa treatment is still unsatisfactory with respect to its profile of side-effects. Psychiatric side-effects (especially depression) are frequently seen in systemic therapy with human recombinant interferon alfa (Kraus et al. 2003). There are known hormonal effects of interferon alfa (e.g. on thyroid hormone metabolism (Corssmit et al. 1995)) – however, the extent of hormonal changes during interferon alfa therapy of chronic hepatitis C for up to 1 year is still not clear.
In addition, potential associations of hormonal changes with psychiatric symptoms such as depression or sexual dysfunction especially in male patients have yet to be documented. Occasionally, male hepatitis C patients on interferon alfa therapy report on noticeable symptoms such as sexual dysfunction or libido loss (Soto Alvarez et al. 1991). This may indicate a specific side-effect of interferon therapy, which possibly reduces quality of life and additionally adherence to antiviral therapy. Until now, it is not clear whether this is solely due to increased depression or whether this can be partially explained by hormonal changes.
Therefore, we prospectively investigated timing and intensity of psychiatric symptoms (especially depression), sexual satisfaction and hormonal changes (especially serum androgen levels) induced by therapy with recombinant human interferon alfa-2b in male patients with chronic hepatitis C.
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Subjects and Methods |
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Thirty-seven consecutive male outpatients were included in our study. Chronic hepatitis C was diagnosed at our institution or the patients had been referred for antiviral therapy of known chronic hepatitis C.
All patients had documented antibodies to hepatitis C virus (HCV) and circulating HCV-RNA as measured by RT-PCR (Cobas Amplicor HCV Monitor test; Roche Diagnostics).
Exclusion criteria were: age under 18 or above 65 years, coinfections (HBV or HIV), severe internal diseases (e.g. cancer, ischemic heart disease, autoimmune disease), psychiatric illness (severe depression or psychosis etc.), active i.v. drug use or alcohol abuse, obvious intellectual impairment or insufficient knowledge of the German language. In addition, the use of antidepressants (especially with dopaminergic effects) was an exclusion criterion due to their known interference with serum hormone levels.
If liver cirrhosis was already present, it had to be well compensated (Child A, Child–Pugh Classification).
All patients gave informed consent to study participation before enrollment. The study protocol was approved by the ethics committee (for medical research) of Würzburg University in accordance with the Declaration of Helsinki.
Study design
The study was designed as a prospective longitudinal single-center study.
Three out of 37 (8.1%) patients could not be included in the final evaluation and statistical analysis: two patients terminated therapy prematurely within the first 3 months because of intolerable side-effects (depression, flu-like symptoms), and one patient withdrew his consent to study participation. Thirty-four patients finally completed the study.
According to the corresponding recommendations in Germany during the recruitment phase, patients were treated with interferon alfa-2b (as opposed to pegylated interferon representing the current therapy standard) alone (n=19) or combination therapy (starting in August 1998, n=15) with interferon alfa-2b plus ribavirin.
The interferon alfa-2b (Intron A) used in the study was obtained from Essex Pharma, Munich, Germany, a subsidiary of Schering-Plough, Kenilworth, NJ, USA.
In case of virological response, 5 MIU interferon alfa-2b ± ribavirin three times weekly were given for up to 12 months. Patients on antiviral combination therapy with interferon alfa-2b and ribavirin received oral ribavirin (800–1200 mg daily).
In all eligible patients, psychometric scores and laboratory data were obtained before therapy (t1), after 4 weeks (t2) and 3–4 months (t3) of treatment as well as 4–6 weeks (t4) after termination of therapy. As there were several patients (genotype 2 or 3) with a total treatment period of 6 months, we did not use an evaluation time point during interferon therapy after t3.
Blood samples were obtained during the patients’ medical visits at time points t1–t4 for measurement of blood count, transaminases, HCV-RNA and hormone serum levels. Genotype identification and liver biopsy (staging and grading: inflammation, fibrosis, cirrhosis) were performed once before therapy. The mode of infection was documented.
Psychometric instruments/questionnaires
Depression: the Hospital Anxiety and Depression Scale (HADS) Depression was assessed by the well-validated HADS, German version, as published by Herrmann et al.(1995). HADS is a 14-item questionnaire with the dimensions anxiety and depression. All items exclusively refer to the emotional state and do not reflect somatic symptoms (Herrmann et al. 1995).
Self-assessment of male sexual dysfunction Libido/sexual satisfaction was assessed by the SCL-90-R, Symptom Checklist-90 Items Revised (Derogatis 1975, German version, as published by Franke (1995)) by item 5. The questionnaire contains one item (‘loss of sexual interest or pleasure’) exclusively referring to libido. In addition, we used a (self-developed) five-point Likert rating scale (‘no limitation’ to ‘complete dysfunction’; 0–4 points) for the corresponding self-assessment.
Assays/serum hormone levels
Blood samples were immediately centrifuged at 4 °C and serum supernatant frozen at – 20 °C. All analyses were performed in duplicates by analytical personnel. Commercially available high-sensitivity immunoassays were used according to the manufacturer’s protocols, and each subject’s samples were run concurrently. Unless otherwise stated, all coefficients of variation for interassay and intraassay variation were below 8.5%. For all assays it has been confirmed that the presence of bilirubin in concentrations up to 100 mg/l, hemoglobin (hemolysis) up to 300 mg/dl and triglycerides up to 1000 mg/dl do not interfere with precision of the assays.
Serum levels of the following hormones were measured: testosterone (free and total testosterone), sex hormone-binding globulin (SHBG), prolactin, dehydroepiandrosterone sulfate (DHEAS), luteinizing hormone (LH) and follicle stimulating hormone (FSH).
The normal range for each parameter reflects the intervals specifically determined by the analytical laboratory of the institution.
The following assays were used. Total testosterone was assayed by a solid-phase, competitive chemiluminescent enzyme immunoassay on an Immulite 1000 Analyzer (Diagnostic Products Corporation, Los Angeles, CA, USA) with intraassay variability (coefficient of variation) <6% and interassay variability <7.5%. The expected normal range for men aged 20–55 years is 270–1070 ng/dl. Free testosterone was assayed by an RIA (Diagnostic Systems Laboratories, Sinsheim, Germany) with intraassay variability (coefficient of variation) <7.5% and interassay variability <6%. The expected normal range for men aged 20–55 years is 14–42 ng/l. In this study, serum testosterone levels are analyzed at a single time point in duplicates and reflect non-fasting serum concentrations. SHBG was assayed by an ELISA (Diagnostic Systems Laboratories). Prolactin, DHEAS, LH and FSH were assayed by solid-phase, competitive chemiluminescent enzyme immunoassays on an Immulite 1000 Analyzer. The expected normal ranges for men aged 20–55 years are 53–360 mIU/L for prolactin, 80–560 µg/dl for DHEAS, 0.8–7.6 IU/l for LH and 1.5–14 IU/l for FSH.
Serum albumin levels were monitored for all study patients throughout the study period.
Statistical analysis
Data were registered and analyzed using the Statistical Package for Social Sciences (SPSS for Windows, German version 11.5.1 (SPSS 2002)).
All tests of significance were two-tailed. P values of <0.05 were considered statistically significant. Because of the explorative character of the study we did not consider alfa adjustment in multiple comparisons.
Descriptive analysis Results describing quantitative measures are expressed as means ± S.D. or ± S.E. Qualitative variables are presented as counts and percentages.
Tests of significance Comparison of variables representing categorical data was performed using the chi-squared test.
Group means of dependent samples (e.g. time course of continuous variables) were compared by means of repeated-measures ANOVA (general linear model procedure, repeated-measures design). Corresponding contrasts were analyzed by paired t-tests.
Pearson’s correlation was used when appropriate (assessment of associations between quantitative variables).
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Results |
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Table 1
shows baseline characteristics of the 34 patients who were included in the final evaluation.
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Clinical features
Clinical side-effects of interferon alfa – especially with respect to psychiatric symptoms – have previously been reported (Kraus et al. 2003). In accord with these results, HADS depression scores increased significantly (and reversibly after therapy) during treatment with interferon alfa-2b. Corresponding results are displayed in Fig. 1.
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Self-assessment of sexual dysfunction and libido loss
Scores for libido self-assessment declined significantly during the course of interferon alfa therapy. Both SCL-90-R (item 5: ‘loss of sexual interest or pleasure’; P<0.001) and the five-point Likert scale (P<0.001) increased significantly over time during therapy with interferon alfa-2b (and ribavirin). Corresponding results are displayed in Fig. 2.
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Additionally, we performed a subgroup analysis to get insight into whether the observed loss of sexual interest was common in our study sample or restricted to a subgroup of male patients.
There were 15 out of 34 patients (44.11%) indicating a decline in sexual interest/satisfaction in both administered scales and 22 out of 34 male hepatitis C patients (64.71%) confirmed libido loss on at least one of the psychometric scales (comparison between evaluation time points t1 and t3).
The type of interferon therapy administered (monotherapy vs combination therapy with additional ribavirin) had no significant effect on the incidence rate of symptoms of libido loss during antiviral therapy (chi square test; P>0.350).
Effect of interferon alfa-2b therapy on (sex) hormone levels
SHBG, LH Serum levels of SHBG (P=0.614) and LH (P=0.810) did not change significantly over time in our study group (repeated-measures ANOVA; P>0.05). Albumin levels were within the normal range throughout the study period (data not shown).
Testosterone
By means of repeated-measures ANOVA, we were able to detect the following significant hormone changes over time. First, we observed a marked decrease over time of testosterone serum levels (Fig. 3). As shown in Fig. 3A, compared with baseline values, free testosterone levels declined significantly during therapy with interferon alfa-2b and ribavirin (repeated-measures ANOVA: main effect time: P<0.001). Four weeks after the end of therapy (t4), this reduction was still persistent.
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). However, there was a minimum of observed mean total testosterone concentration at t3, with a clear tendency towards reversibility after the end of interferon treatment (t4).
DHEAS, prolactin
DHEAS serum concentrations declined significantly (P=0.012) during interferon alfa-2b medication with a minimum already at t2, 4 weeks after initiation of antiviral therapy (Fig. 4). The respective values tended towards restoration of baseline data at t4, about 4 weeks after termination of antiviral medication.
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Relationship between libido loss, interferon-induced depressive symptoms and hormonal changes during interferon alfa-2b therapy
As male sexual arousal disorder may be affected by both hormonal and psychological factors, we analyzed inter-correlations between therapy-associated libido loss and increase in depression scores or changes in hormone levels respectively. The following analyses are based on observed changes between t1 (baseline data) and t3, 3–4 months after initiation of antiviral therapy (Table 2).
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However, there is also a significant negative correlation between free testosterone concentrations during therapy and sexual dysfunction scores at t3 (r= – 0.42; P=0.038). Therefore, to some degree, decreased levels of free testosterone are linked with symptoms of male sexual arousal disorder. Rise of prolactin serum levels was not significantly associated with free testosterone reduction in our study (r= – 0.21; P>0.05; see Table 2). These results indicate an effect of interferon therapy on male gonadal steroid biosynthesis independent from control actions of prolactin on androgen production. Moreover, interferon-associated depressive symptoms and changes in sex hormone levels are not directly linked (|r|<0.27; P>0.05) in male hepatitis C patients during interferon alfa therapy (Table 2).
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Discussion |
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The patients in our study showed significantly increased depression scores during the treatment period, and we could also confirm previous patients’ reports on interferon-associated libido loss (Soto Alvarez et al. 1991).
The assessment of interferon-induced changes in sex hormone serum levels has been so far limited to small studies (Barreca et al. 1993, Kauppila et al. 1997, Corssmit et al. 2000, Weidinger et al. 2002), case reports or animal models (Hibi et al. 1997, Montor et al. 1998).
In accord with Barreca et al.(1993) and Corssmit et al.(2000), we observed a significant decline of free and total testosterone serum concentrations within the normal range over time. As testicular function is known to be controlled by gonadotropins (LH, FSH) and is affected by prolactin, we evaluated the time course and concentrations of gonadotropins and prolactin. LH levels (as well as FSH serum concentrations) were not significantly affected during interferon alfa-2b treatment. Therefore, we assume that the observed testosterone decrease is not mediated by alteration of the pituitary–testicular axis. This, however, cannot be entirely excluded as gonadotropin secretion pulsatility was not analyzed.
An explanation for the apparent discrepancy between total and free testosterone levels at t4 remains open. We confirmed, however, that differences are not due to changes in SHBG levels. This is consistent with the findings of Corssmit et al.(2000). We are aware that the best measures for bioavailable testosterone are represented by either concentrations of free testosterone measured by equilibration dialysis assays or free testosterone calculated from albumin and SHBG levels (Christ-Crain et al. 2004a). However, we believe that in this particular study, direct measurement of free testosterone is equally representative (of male androgen status) because it has been demonstrated that within the physiological range of 40–50 g/l (5.8–7.2 x 10–4 mol/l) of albumin binding protein concentrations do not significantly affect free testosterone levels (Vermeulen et al. 1999). As indicated, in our study the patients’ albumin levels stayed within the normal range throughout the whole evaluation time.
Elevated levels of prolactin are associated with sexual dysfunction, such as reduced libido, erectile dysfunction, diminished ejaculate volume and oligospermia (Spollen et al. 2004). In our study, mean serum prolactin levels were significantly increased during interferon therapy. As it has been demonstrated that the duration and frequency of prolactin secretory bursts from the pituitary are independent from gonadal steroid plasma levels in women and in men (Genazzani et al. 1994), we assume that the observed increase in mean serum prolactin values is not secondary to alterations in gonadal steroid concentrations. Rather we may speculate that interferon therapy either directly affected lactotrope cells in the pituitary, or hypothalamic factors which control prolactin secretion, or both. Elevated serum levels of prolactin during interferon therapy, however, did not significantly correlate with reductions in free testosterone serum concentrations. Therefore, we conclude that prolactin elevation did not contribute to reduced testosterone concentrations and impairment of libido.
In this context, it is important to add that none of the hepatitis C patients in our study received antidepressant medication known to exert dopaminergic effects as a confounding factor in the evaluation and interpretation of increased prolactin levels during interferon alfa-2b medication.
A marked association between the androgen-precursor DHEA and libido has been demonstrated in females (Arlt et al. 1999). Therefore, we monitored DHEAS levels before, during and after interferon therapy. The reversible decline of DHEAS serum concentrations during antiviral treatment may be explained either by direct effects on the adrenal cortex or by indirect mechanisms involving the adrenocorticotropic hypothalamic–hypophyseal–adrenal axis via corticotropin-releasing hormone/adrenocorticotropin. Alternatively, the decline of serum DHEAS in parallel with the observed reductions in total and free testosterone values during interferon therapy may be due to direct affects on the testes in the male patients.
The sexual arousal disorder in our study population was linked to both interferon-induced depressive symptoms and serum free testosterone decline (confirming the results of studies that did not find a significant correlation between total testosterone and symptoms of hypogonadism (Christ-Crain et al. 2004b)). However, we found no direct link between sex hormone changes and depression. This implies that both factors (interferon-induced depression and functional androgen deficiency) may independently affect the extent of male sexual dysfunction in patients with chronic hepatitis C and therapy with interferon alfa-2b. It is important to note that we do not postulate a causative relationship for each single factor (depression, androgen deficiency) – in contrast we propose that both may be permissive with respect to symptoms of sexual dysfunction.
As it is known that relatively low androgen levels generally suffice for normal sexual function, the results of the study do not allow us to define low testosterone serum concentrations as the main cause for sexual dysfunction in the study population. These may, however, represent among others, such as depression, a permissive factor for libido loss.
There are several limitations in our study that have to be kept in mind when drawing conclusions from the findings. Hormonal changes associated with interferon alfa-2b therapy were within the normal ranges throughout the evaluation period and therefore have to be interpreted with care. Sample size in our study does not exceed 34 male patients, although the sample population was quite homogeneous and target variables are clear. Therefore, from a statistical point of view this specific sample size provides enough power to detect relevant changes of target variables. Further limitations include the fact that conventional interferon alfa-2b has been used (as opposed to pegylated forms representing the current therapy standard) and that information on sexual dysfunction was obtained by a psychometric instrument that is not validated or referenced with larger study populations.
In summary, we found that treatment with recombinant interferon alfa-2b in male patients with chronic hepatitis C is associated with functional androgen deficiency. This decline in testosterone is partially linked to therapy-induced symptoms of libido loss and may be due to direct effects of interferon on the gonads or effects on hypothalamic regulatory centers. However, there is an even stronger correlation between symptoms of sexual arousal disorder and interferon-induced depression in these patients.
Subsequent studies should include larger sample sizes (anticipated alfa-level adjustment and corresponding sample size calculations) as well as specific hypothesis-driven analyses based on the presented findings.
In clinical practice, during the workup of patients with chronic hepatitis C it could be helpful to perform baseline hormone screening prior to the initiation of interferon therapy. Potential interferon-associated symptoms of libido loss and therefore reduced quality of life could hence be better put into context during treatment period (depression vs hormonal changes).
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Acknowledgements |
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Funding |
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This study was supported in part by an unrestricted grant of Essex Pharma, Munich, Germany (a subsidiary of Schering–Plough, Kenilworth, NJ, USA). M R K is a member of the Scientific Advisory Board of Essex Pharma, and has served on speakers bureaus for Shering–Plough and Essex Pharma.
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References |
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Received 28 January 2005
Accepted 23 February 2005
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| HOME | HELP | CONTACT US | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
