Idiopathic hypersomnia: clinical features and response to treatment

Mohsin Ali, R Robert Auger, Nancy L Slocumb, Timothy I Morgenthaler, Mohsin Ali, R Robert Auger, Nancy L Slocumb, Timothy I Morgenthaler

Abstract

Objective: A recent American Academy of Sleep Medicine publication identified a need for research regarding idiopathic hypersomnia. We describe various clinical and polysomnographic features of patients with idiopathic hypersomnia, with an emphasis on response to pharmacotherapy.

Methods: A retrospective review of our database initially identified 997 patients, utilizing "idiopathic hypersomnia", "hypersomnia NOS", and "primary hypersomnia" as keywords. The charts of eligible patients were examined in detail, and data were abstracted and analyzed. Response to treatment was graded utilizing an internally developed scale.

Results: Eighty-five patients were ultimately identified (65% female). Median (interquartile range) ages of onset and diagnosis were 19.6 (15.5) and 33.7 (15.5), respectively. During a median follow-up duration of 2.4 (4.7) years, 65% of patients demonstrated a "complete response" to pharmacotherapy as assessed by the authors' grading schema. Methylphenidate was most commonly used as a first-line agent prior to December 1998, but subsequently, modafinil became the most common first drug. At the last recorded follow-up visit, 92% of patients were on monotherapy, with greater representation of methylphenidate versus modafinil (51% vs. 32%). Among these patients, methylphenidate produced a higher percentage of "complete" or "partial" responses than modafinil, although statistical significance was not reached (38/40 [95%] vs. 22/25 [88%], respectively, p = 0.291).

Conclusions: The majority of patients with idiopathic hypersomnia respond well to treatment. Methylphenidate is chosen more often than modafinil as final monotherapy in the treatment of idiopathic hypersomnia, despite the fact that it is less commonly used initially. Further prospective comparisons of medications should be explored.

Figures

Figure 1
Figure 1
Difference between patients' reported sleep time and actigraphically recorded sleep time. At the time of initial consult, average sleep time was obtained by review of the sleep schedule with the patient. Prior to polysomnography, actigraphy was obtained in 61 (72%) of our patients. Above, we compare the subjective sleep duration with the subsequent actigraphically estimated sleep time, using the Bland-Altman method. The vertical red line represents 7.94 hours, the average of the mean between all paired subjective and actigraphic hours of sleep. The horizontal red line represents the mean difference between actigraphically measured and reported sleep, and the dotted red lines represent the SEM (−0.99 ± 0.18 hours [p

Figure 2

Limiting side effects. Side effects…

Figure 2

Limiting side effects. Side effects or complaints that limited the ability to increase…

Figure 2
Limiting side effects. Side effects or complaints that limited the ability to increase medication dose or that required discontinuation of the medication are shown above. Notably, the high cost of medication was a common limiting complaint for modafinil and methamphetamine. Hypertension developed in some patients taking methamphetamine, modafinil, and pemoline; causality is not established, however, as the development of hypertension may have been coincidental. Nonetheless, the treating physicians did not feel comfortable continuing the medication under these circumstances.
Figure 2
Figure 2
Limiting side effects. Side effects or complaints that limited the ability to increase medication dose or that required discontinuation of the medication are shown above. Notably, the high cost of medication was a common limiting complaint for modafinil and methamphetamine. Hypertension developed in some patients taking methamphetamine, modafinil, and pemoline; causality is not established, however, as the development of hypertension may have been coincidental. Nonetheless, the treating physicians did not feel comfortable continuing the medication under these circumstances.

Source: PubMed

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