Testosterone Treatment in Multiple Sclerosis: Title and subTitle BreakA Pilot Study FREE

During reproductive ages, there is a distinct female preponderance of autoimmune diseases, including multiple sclerosis (MS).¹ Sex hormones and/or sex chromosomes may be responsible for this enhanced susceptibility. The female-male ratio is greater in patients presenting with MS before the age of 20 years (3.2:1.0) compared with the ratio in the population with MS as a whole (2:1).² In males, the onset of MS tends to be later in life (30s-40s), as bioavailable testosterone levels decline.³

Testosterone has a protective effect in many animal models of autoimmune disease,¹ including the most widely used animal model of MS, experimental autoimmune encephalomyelitis.^{4 - 5} Testosterone treatment has been shown to be immunomodulatory in vivo and in vitro,^{1 ,4 ,6} consistent with observations that testosterone treatment is protective not only for experimental autoimmune encephalomyelitis, but also for other autoimmune diseases, such as lupus, arthritis, and diabetes mellitus, which do not have the central nervous system as the target organ.^{7 - 9} In experimental autoimmune encephalomyelitis physiologic levels of endogenous testosterone were protective in some, but not all, genetic backgrounds, while treatment with exogenous testosterone was protective across various genetic backgrounds.¹⁰

In addition to being immunomodulatory, testosterone has been shown to be neuroprotective in several models of neurodegenerative disease.¹¹ In humans, it may improve cognitive function in hypogonadal healthy men,¹² and in men with Alzheimer disease.¹³ In light of the well-described neuroprotective effects of estrogens,¹⁴ mechanisms underlying the neuroprotective effects of testosterone treatment may involve its conversion to estrogen by aromatase.¹⁵ On the other hand, testosterone treatment has been shown to be toxic to cultured oligodendrocytes.¹⁶ Thus, it is unknown whether testosterone treatment would be beneficial or detrimental in those with MS.

Previously, neuroimaging studies in 413 subjects, comparing women and men with MS, have been conducted to reveal some insights into the effect of testosterone in MS. Men had fewer contrast-enhancing lesions than women, but had a higher likelihood for them to evolve into T1-weighted “black holes.”¹⁷ These data were consistent with the observation that men are less likely to develop MS, but when they do, it tends to be more severe clinically.^{3 ,18 - 19} In a follow-up study²⁰ of 35 women and 25 men with relapsing-remitting MS (RRMS), the finding of fewer enhancing lesions in men was confirmed, but the increased likelihood for lesions to evolve into T1-weighted black holes in men was not, perhaps because of the smaller sample size.

Finally, testosterone treatment is frequently used to improve muscle mass and bone mineral density in elderly hypogonadal men, and in men with various chronic diseases,²¹ but the effects in MS are not known. Thus, to investigate possible effects of testosterone treatment in those with MS, testosterone was administered via transdermal gel application (AndroGel; Solvay Pharmaceuticals, Inc, Marietta, Ga) to men with RRMS to investigate safety and tolerability, as well as effects on clinical disability and brain magnetic resonance imaging (MRI).

Men aged 18 to 65 years who met the Poser criteria for clinically definite RRMS, were not receiving disease-modifying treatment, and had an Expanded Disability Status Scale score of 0 to 5.0 were studied. Subjects had to have at least 1 clinical relapse (worsening of a preexisting symptom or appearance of a new symptom, each over 0-3 days) or the appearance of at least 1 greater than 3-mm gadolinium-enhancing lesion on brain MRI during the preceding 2 years. The protocol was approved by the University of California, Los Angeles (ULCA) Human Subjects Protection Committee and the institutional review board of the Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center.

Given the small sample size of this initial pilot study, each subject served as his own control, thereby minimizing the effect of interindividual heterogeneity of disease, as described.²² There was a 6-month pretreatment observation period (months −6 to 0), followed by a 12-month (months 1-12) treatment period with 10 g of the gel containing 100 mg of testosterone (AndroGel), applied to the upper arms once per day. The Table provides details regarding the timing of clinical and laboratory measures obtained.

Contrast-enhanced brain MRIs were obtained on an MRI unit (1.5-T Sonata unit; Siemens, Erlangen, Germany). Brain atrophy measures were obtained from the volumetric T1-weighted scans using fully automated software (SIENA)²³ for each month compared with the initial baseline scan (month −6). Normalized brain volumes were calculated for the initial baseline scan using computer software (SIENA-X).²³ Enhancing lesion numbers were determined once by a neuroradiologist blind to details of the study design and second by a single investigator (N.L.S.) blind to the study month. Consensus was reached by a third review by a trained neuroradiologist in cases of differing initial counts. Enhancing volumes were determined using a semiautomated seed-growing technique using customized versions of existing software.²⁴ T2-weighted lesion volumes were determined using a custom-automated threshold-based algorithm.

Spearman rank correlations were used to assess the relationship between baseline imaging and testosterone levels. Percentage change in the cognitive measures and mean changes in T2-weighted volumes and T1-enhancing lesion numbers and volumes were evaluated using the t test for means and the Wilcoxon signed rank test for medians. To assess brain volume changes, a percentage change in brain volume against time scatterplot with a Loess regression curve was produced, and a first-degree spline model was developed. This model fitted line pieces for pretreatment and early treatment periods (months −6 to 3) and treatment response period (months 3-12), and these pieces were joined to achieve continuity. Slopes of these lines were estimated and compared. A random intercept was set in the model to allow the difference among subjects. Age, testosterone level, and baseline brain volume did not show significant correlation with the change of brain volume; therefore, these factors were not included in the model. Linear regressions were also used to determine slopes of brain volume changes for each 6-month interval during the 18-month study period. SAS statistical software (SAS Institute Inc, Cary, NC) was used to perform the analysis, and all tests were 2-sided, with type I error .05.

Eleven subjects with RRMS were enrolled in the study. One subject discontinued participation after moving out of the area at study month −4, and no data from this subject were included in the analysis. The mean age of the subjects was 46 (range, 29-61) years. The median disease duration was 12.5 (range, 0.5-25.0) years. The median Expanded Disability Status Scale score was 2.0 (range, 1.5-2.5).

At baseline, all subjects had testosterone levels in the lower range of normal, with a mean of 493 ng/dL (17.1 nmol/L) (range, 321-732 ng/dL [11.1-25.4 nmol/L]). During daily treatment with 10 g of the gel containing 100 mg of testosterone, serum testosterone levels increased 50% on average to the higher range of normal (Figure 1).

Lean body mass (muscle mass) increased significantly during treatment, with a mean increase of 1.7 kg at month 12 of treatment compared with pretreatment levels (P = .02). Hip and spine bone density, as measured by the dual energy x-ray absorptiometry scan, were normal at baseline and remained unchanged during the study.

There were no subjective reports of adverse effects and no significant abnormalities in any blood test results. Prostate examination results were stable throughout the study. One subject necessitated placement of a cardiac stent, but this was not thought to be drug related because he had preexisting risk factors for coronary artery disease.

Scores from the Paced Auditory Serial Addition Task (PASAT) component of the Multiple Sclerosis Functional Composite remained stable during the first 6 months of treatment (months 3 and 6), trended upward after 9 months, and were significantly improved by month 12 of treatment (Figure 2). During the baseline pretreatment phase, there was clearly a practice effect, as previously described.^{25 - 27} Thus, to avoid the confound of this practice effect in interpreting the effect of treatment, PASAT performance during months 9 and 12 of treatment was compared with performance at month 0 of baseline, not month −6 or −3. Consistent with an improvement in the PASAT during month 12 of testosterone treatment, there was also a trend for improvement in spatial memory in immediate (P = .07) and delayed (P = .06) recall subtests of the 7/24 Spatial Recall Test at treatment month 12. No changes were observed in the Expanded Disability Status Scale score, the 9-Hole Peg Test, or the 25-ft timed walk.

The group had low levels of enhancing lesion activity at baseline (median number, 0; median volume, 0.04 cm³), which had no relationship to baseline testosterone levels and which was not significantly increased or decreased with treatment (numbers, P  = .31; volumes, P  = .94). T2-weighted lesion volumes were not significantly different comparing the observation and treatment periods (mean T2-weighted volume, 11.78 vs 12.51 cm³; P = .21).

At study onset, the mean normalized whole brain volume was 0.82 (range, 0.78-0.84) and was negatively correlated with age (P = .05); however, there was no relationship between baseline brain volumes and baseline testosterone levels (r = 0.18). During the first 9 months of the study, brain volumes decreased at an annualized rate of −0.81% (P<.001). During the subsequent 9 months of testosterone treatment, brain atrophy slowed to an annualized rate of −0.26% (P = .10). This represented a 67% reduction in the rate of brain volume loss compared with the pretreatment period (Figure 3). Similarly, when linear regressions were used to estimate slopes at 6-month intervals, there was an annualized atrophy rate of −0.79% (P = .04) during the pretreatment period (study months −5 to 0), a rate of −0.58% (P = .02) during early treatment (study months 1-6), and a rate of −0.22% (P = .44) during later treatment (study months 7-12).

This is a small exploratory study of treatment of male patients with RRMS with testosterone gel for 1 year. A crossover design, using a within-arm comparison of pretreatment to treatment, was used to reduce the effect of disease heterogeneity given the small sample size, as previously described.²²

The PASAT component of the Multiple Sclerosis Functional Composite showed significant improvement at month 12 of testosterone treatment. Practice effects are common when the PASAT is administered serially. Previous reports^{25 ,27} demonstrated that PASAT performance stabilizes after the third session, and this effect was evident when between-session timing was as brief as 1 week or as long as 6 months. In our study, PASAT performance was tested every 3 months and performance also stabilized after 3 trials, with these 3 trials all in the 6-month pretreatment baseline period. Subsequently, PASAT performance remained unchanged for the first 6 months of testosterone treatment. Then, a gradual improvement in performance was observed during the last 6 months of treatment, reaching significance at month 12. While it is theoretically possible that PASAT improvement at 9 and 12 months of treatment could reflect a second wave of practice effects, to our knowledge this has never been previously reported in placebo-treated arms of clinical trials, including those involving large cohorts of patients with MS followed up for up to 2 years.²⁶ Our observed improvement in PASAT performance, combined with trends for improvements in the 7/24 Spatial Recall Test, is consistent with previous reports^{28 - 29} of testosterone-mediated improvements in working and spatial memory in healthy nonhypogonadal elderly men. Interestingly, the timing of these cognitive improvements coincided with a slowing of brain atrophy on MRI.

Measures of inflammatory activity on MRI did not decrease significantly after treatment with testosterone, which may be because of the relatively low levels of inflammatory activity present at baseline. Despite the fact that inclusion criteria required either a relapse or enhancing lesion activity in the 2 years prior to enrollment, the exclusion of subjects taking disease-modifying treatments likely created a selection bias toward subjects with a relatively milder clinical disease and less inflammatory activity on MRI. Thus, in this subject group, we can only conclude that testosterone treatment did not significantly increase inflammatory activity on otherwise relatively quiescent MRIs.

Previous studies in noninflammatory conditions have shown that testosterone can affect brain volumes independent of effects on inflammation. Men with Klinefelter syndrome have androgen deficiency and smaller left temporal lobe volumes,³⁰ and testosterone supplementation during development led to larger gray matter volumes in the left temporal lobe and improved verbal fluency scores in these patients.³¹ In our study, brain atrophy rates were determined by dividing the 18-month study period into 9-month intervals, which includes the first 3 months of treatment with the baseline period of observation. This approach is consistent with other reports assessing the effects of treatment on brain atrophy,³² and takes into account the likelihood that neuroprotective effects are unlikely to be evident until several months of treatment have occurred. The mean annualized brain atrophy rate of −0.81% observed during the first 9 months of this study was consistent with previous rates observed in patients with MS.³³ During the last 9 months of treatment, the rate of atrophy slowed to −0.26%, representing a decrease of 67%. Because the protective effect of testosterone treatment on brain atrophy was observed in the absence of an appreciable anti-inflammatory effect, this protection may not be limited to MS, but may be applicable to those with noninflammatory neurodegenerative diseases.

As is the case with any initial pilot clinical trial, conclusions from our study must be made with caution primarily because of the small sample size. Also, findings in our study may or may not be applicable to subjects with MS with more aggressive disease. Overall, in this first trial of testosterone treatment in men with RRMS, the treatment was shown to be safe and well tolerated, and led to increases in lean body mass. In addition, exploratory findings reported herein suggest a possible neuroprotective effect of testosterone treatment in men, which warrants further investigation.

Correspondence: Rhonda R. Voskuhl, MD, Department of Neurology, The David Geffen School of Medicine at UCLA, Neuroscience Research Bldg, Room 475D, 635 Charles Young Dr S, Los Angeles, CA 90095 (rvoskuhl@ucla.edu).

Accepted for Publication: December 14, 2006.

Author Contributions:Study concept and design: Sicotte, Steiner, Swerdloff, and Voskuhl. Acquisition of data: Sicotte, Giesser, Tandon, Klutch, Steiner, Drain, Hull, and Voskuhl. Analysis and interpretation of data: Sicotte, Tandon, Shattuck, Wang, Elashoff, Swerdloff, and Voskuhl. Drafting of the manuscript: Sicotte, Giesser, Hull, Wang, and Voskuhl. Critical revision of the manuscript for important intellectual content: Sicotte, Giesser, Tandon, Klutch, Steiner, Drain, Shattuck, Elashoff, Swerdloff, and Voskuhl. Statistical analysis: Wang and Elashoff. Obtained funding: Sicotte and Voskuhl. Administrative, technical, and material support: Giesser, Tandon, Klutch, Steiner, Drain, Shattuck, Hull, and Swerdloff. Study supervision: Sicotte, Giesser, Steiner, Swerdloff, and Voskuhl.

Financial Disclosure: None reported.

Funding/Support: This study was supported by grants RG3239 and JF2107 from the National Multiple Sclerosis Society; grant MO1 RR00425 from the General Clinical Research Centers at Harbor-UCLA Medical Center; the Sherak Family Foundation; and the Skirball Foundation.