Abstract
Background and purpose:
The aim of this study was to systematically review the efficacy and tolerability of gabapentin in the treatment of sleep disturbance in patients with medical illness.
Methods:
PubMed was searched for randomized, double-blinded, placebo-controlled trials that reported sleep changes during gabapentin treatment up to November 2015.
Findings:
This review included 26 studies involving 4,684 participants. Except for Composite Endpoint 3 [standardized mean difference (SMD) = 0.09, 95% confidence interval (CI): −0.05–0.22] compared with the placebo group, the gabapentin group showed superior outcomes on our endpoints: Composite Endpoint 1 (SMD = 0.50, 95% CI: 0.28–0.71), Composite Endpoint 2 (SMD = −0.53, 95% CI: −0.77 to −0.30), Composite Endpoint 4 (SMD = −0.38, 95% CI: −0.58 to −0.19), Composite Endpoint 5 [risk ratio (RR) = 1.79, 95% CI: 1.24–2.58], and Composite Endpoint 6 (RR = 0.48, 95% CI: 0.32–0.72). However, the patients in the gabapentin group showed worse tolerance than those in the placebo group (RR = 1.38, 95% CI: 1.08–1.76).
Implications:
This study is the first to systematically assess the clinical value of gabapentin for the treatment of sleep disorders. We found that regardless the type of sleep outcomes, gabapentin displayed stable treatment efficacy for sleep disturbance in patients with medical illness. However, when an average dose of approximately 1,800 mg/day was used, the risk of treatment discontinuation or drug withdrawal was relatively high. We recommend that further studies confirm these findings in patients with primary sleep disorders.
Introduction
Sleep disorders have been always a disturbing public health issue, not only because they affect quality of life, increase the patient’s risk of cardio-cerebrovascular disease (1, 2) and death (2, 3), weaken social productivity, and increase medical burdens (4, 5) but also because unlike other diseases with a phase-wise pattern, they cannot be cured using multiphase treatment. Although phenobarbital, benzodiazepine hypnotics, Z-drugs, antidepressants, and melatonin receptor agonists can all contribute to a certain extent (6, 7), few of these treatments can either restore patients’ normal sleep structure or completely cure sleep disorders.
Gabapentin, an apha-2-delta voltage-gated calcium channel ligand (8) that is widely used for the treatment of epilepsy, neuropathic pain, and restless legs syndrome, can enhance slow-wave sleep in both normal individuals (9) and epileptic patients (10, 11) and can improve slow-wave sleep and sleep efficiency and reduce nighttime awakening in patients with primary sleep disorders (12). However, these findings have not been verified with randomized controlled trials. Clinical studies have revealed that gabapentin could improve the objective and subjective outcomes of sleep disturbance in patient with medical illness (13–37). Gabapentin Enacarbil (GEn) or XP13512 is a prodrug of gabapentin, used as an anticonvulsant and for pain relief in postherpetic neuralgia. This new formulation of gabapentin was designed for increased oral bioavailability over gabapentin. It provides reliable drug absorption and consistent bioavailability (16). Nevertheless, the results derived from these studies had certain inconsistencies and did not undergo any systematical evaluation. Through a systematic review of the use of gabapentin to treat restless legs syndrome, neuropathic pain, alcohol dependence, hot flashes in menopause, fibromyalgia, phantom limb pain, human immunodeficiency virus (HIV)-associated sensory neuropathies, and bipolar disorder, this study attempted to evaluate the efficacy and tolerability of gabapentin for the treatment of sleep disturbance in patients with medical illness.
Materials and Methods
This systematic review and meta-analysis were performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement (PRISMA) (38). There are no ethical issues involved in our study because our data were based on published studies.
Data Sources and Search
PubMed was searched for all clinical trials related to the present research topic (up to November 8, 2015). The keywords selected from the Medical Subject Headings (MeSH) included intervention, study type, and endpoint event. The search range was “title/abstract/keywords.” No language restrictions were applied. In addition, we screened the reference lists of all included trials to identify additional eligible studies. Detailed information regarding the search terms used in the literature search is provided in the Supplementary Material.
Study Selection
Eligible Trials
(1) Participants: all included patients were 18 years or older and had/did not have a record of baseline sleep status; (2) intervention: the patients in the treatment group received gabapentin, gabapentin enacarbil, or XP13512 (Gabapentin), and the patients in the control group received placebos with a treatment duration of at least 7 days; (3) endpoints: all included trials reported sleep changes and treatment discontinuation or drug withdrawal events that were possibly or probably related to the study drugs; (4) study type: randomized, double-blinded, controlled trials were included.
Data Extraction
Using a unified form, two investigators independently extracted the data and created the data spreadsheet, which were then cross-checked to ensure data accuracy. Disagreements were resolved by consensus. The extracted data mainly included the six composite endpoints and treatment discontinuation or drug withdrawal events that were possibly or probably related to the study drugs.
Endpoint Definitions
Because of the diversity of outcomes reported in the included trials, only a limited number of trials provided data that could be pooled for each meta-analysis. To reach a sufficient statistical level, we introduced the concept of “composite endpoint” to pool the data related to sleep outcomes with similar significance and a consistent direction.
Based on the treatment outcomes and relevant data provided by the original trials, seven composite endpoints were analyzed for evaluation. Composite Endpoints 1–6 were used to evaluate the efficacy of gabapentin, and Composite Endpoint 7 was used to evaluate treatment discontinuation or drug withdrawal events that were possibly or probably associated with gabapentin. Composite Endpoints 1–4 indicated sleep improvement after treatment. Specifically, Composite Endpoint 1 represented the net increase in the evaluation indices provided in the trials in which the index values increased, but the baseline values were not provided. Composite Endpoint 2 represented the net decrease of evaluation indices provided in the trials in which the index values decreased but the baseline values were not provided. Composite Endpoint 3 and Composite Endpoint 4 represented the posttreatment values of the evaluation indices provided in the trials in which the index values increased and the trials in which the index values decreased (none of these trials provided the baseline values), respectively. Composite Endpoint 5 (Excellent, 0 or Good) represented the sleep outcomes that received the highest grades in the survey, e.g., the overall quality of sleep was evaluated as “Excellent,” or the ability to function was evaluated as “Good,” or the number of nighttime awakenings caused by RLS symptoms was 0, or the number of hours awake per night because of RLS symptoms was 0 in the past week. Composite Endpoint 6 (Poor, ≥3, ≥5, or 7) represented the sleep outcomes that were graded the lowest in the survey, e.g., the overall quality of sleep was evaluated as “Poor,” or the ability to function was evaluated as “Poor,” or the number of nighttime awakenings caused by RLS symptoms was ≥5, or the number of hours awake per night because of RLS symptoms was ≥3, or the number of nights with RLS symptoms was 7 in the past week.
Quality Assessment
Two investigators evaluated the methodological quality of all included trials according to the Cochrane Collaboration’s tool for assessing bias [the Reviewer’s Handbook (39)].
Grading of Recommendations Assessment, Development, and Evaluation (GRADE) Classification
Based on the GRADE study group criteria (20), we graded the evidence quality for all of the endpoints.
Data Synthesis and Analysis
Based on the formula and endpoint definition, the values of the same endpoints in each trial were pooled first and then the data from different trials were pooled together for analysis. The standardized mean difference (SMD) and risk ratio (RR) were used to assess the abovementioned endpoints. Prior to the meta-analysis of each endpoint, statistical heterogeneity across the various trials was tested using Chi-square test. A P-value greater than the nominal level of 0.10 and I2 ≤40% indicated a lack of heterogeneity across trials, allowing for the use of a fixed-effects model; otherwise, a random-effects model was used. The inverse variance method was used for continuous variables, and the Mantel–Haenszel method was used for dichotomous variables. In addition, a sensitivity analysis was conducted by removing each trial one at a time, and the publication bias was evaluated using the Egger test.
SPSS Predictive Analytics Software version 18.0 (SPSS, Inc., Chicago, IL, USA) was used for the Chi-square tests, and Stata Statistical Software version SE 12.0 (Stata Corp. LP, College Station, TX, USA) was used for all other analyses.
Results
Search Results and Trial Characteristics
Ninety-eight records were identified through database searches and were screened by reading titles, abstracts, and part of main text. After irrelevant papers, observational studies, duplicates, and trials that used non-placebo control drugs were excluded, 26 papers (13–19, 21–37, 40, 41) met the inclusion criteria. The included publications comprised eight RLS-related trials, eight neuropathic pain-related trials, and three alcohol dependence-related trials, two trials involving hot flashes in menopause, one fibromyalgia-related trial, one trial involving phantom limb pain, one trial involving HIV-associated sensory neuropathies, and one bipolar disorder-related trial. Among the included studies, six trials were included only for systematic review and 20 trials were included for meta-analysis.
The included 26 trials involved 4,684 patients. The average follow-up length was 11.07 weeks/per patient, and the total follow-up time was 997.23 patient-years. The average age of 83.50% of the patients was 55.45 (±13.45) years. Among 96.50% of patients, males accounted for 42.73%; among 90.67% of patients, the average length of disease course was at least 6.23 (±9.76) years. The initial dose of gabapentin was 300 or 600 mg/day; after the dose-increasing phase, the minimum dose was 600 mg/day and the maximum dose was 3,600 mg/day, with an average dose of 1,793.92 mg/day. Figure 1 presents the screening process used in the study, Table 1 lists the main characteristics of all included trials.
Figure 1
Table 1
| Reference | Participants | Intervention | Sleep outcome | Study design and treatment duration (weeks) | |||||
|---|---|---|---|---|---|---|---|---|---|
| Diagnoses | Sample size | Age (years)a | Male (%) | Illness duration (years)a | Gabapentin group | Control group | |||
| Anton et al. (13) | Alcohol dependence | 100 | 44.82 ± 9.53 | 82.45 | NR | Gabapentin combined with naltrexone (50 mg/day); gabapentin: the initial dose was 300 mg prior to bedtime, increased to 1,200 mg/day at night from the fifth day | Identical placebo | Insomnia sleep index (42), Epworth Sleepiness Scale (43); adverse effects | RCT; 6 |
| Brower et al. (41) | Alcohol dependence | 21 | 46 (30.8–60)b/44 (41–54)b | 52.38 | NR | Gabapentin: the initial oral dose was 300 mg 45 min before bedtime, increased to 1,500 mg/day at bedtime within 10 days | Identical placebo | Sleep problems questionnaire; Sleep diaries; Polysomnography parameters; adverse effects | RCT; 6 |
| Hahn et al. (21) | Human immunodeficiency virus-associated sensory neuropathies | 25 | 46 (27–59)b/44 (35–61)b | 80 | 0.76 (median) | Gabapentin: the dose was adjusted every 4 days until it reached 1,200 mg/day after more than 2 weeks | Matching placebo | Mean sleep interference scorec; adverse effects | RCT; 4 |
| Rowbotham et al. (30) | Postherpetic neuralgia | 229 | 73 (40–90)b/74 (39–89)b | 52.44 | 2.39 (median) | Gabapentin: the initial dose was 300 mg, increased to 3,600 mg/day at night from the fourth week | Identical placebo | Mean sleep interference scorec; adverse effects | RCT; 8 |
| Rice et al. (29) | Postherpetic neuralgia | 334 | 76.3 (36.1–90.8)d/74.9 (28.9–94.8)d | 41.32 | 2.19 (median) | Gabapentin: the initial dose was 300 mg/day, increased to 1,800 or 2,400 mg/day within 2 weeks | Identical placebo | Mean sleep interference scorec; adverse effects | RCT; 7 |
| Garcia-Borreguero et al. (18) | RLS | 44 | NR | NR | NR | Gabapentin: the dose was initially 600 mg/day and was adjusted every 2 weeks to a maximum dose of 2,400 mg/day (1200 hours and 2000 hours) | Identical placebo | Pittsburgh sleep quality index global score (44); polysomnography parameters; adverse effects | RCT; 6 (excluding the washout period and crossover period) |
| Gordh et al. (19) | Neuropathic pain | 120 | NR | NR | ≥0.5 | Gabapentin: the initial dose was 300 mg/day, increased to 2,400 mg/day from the third week | Identical placebo | Mean sleep interference scoree; adverse effects | RCT; 5 (excluding the washout period and crossover period) |
| Lal et al. (25) | RLS | 217 | 48.0 ± 12.70 | 64.06 | 13.39 ± 13.68 | Gabapentin enacarbil: the initial dose was 600 mg/day, increased to 1,200, 1,800, or 2,400 mg/day within 9 days | Identical placebo | Post-sleep questionnaire; tolerability assessments | RCT; 12 |
| Mason et al. (27) | Alcohol dependence | 150 | 44.53 ± 11.01 | 56.67 | 14.43 ± 9.85 | Gabapentin: the initial dose was 300 mg/day, increased to 900 or 1,800 mg/day within 6 days | Identical placebo | Pittsburgh sleep quality index global score (44); adverse effects | RCT; 12 |
| Bone et al. (40) | Phantom limb pain | 19 | 56.25 ± 17.5 | 78.95 | 1.5 (median) | The first phase was gabapentin treatment (12 weeks): the initial dose was 300 mg/day, gradually increased to 2,400 mg/day; the second phase was placebo treatment (6 weeks), with 1 week of washout between the two phases | 6 weeks of placebo treatment and 12 weeks of gabapentin treatment | Mean sleep interference scorec; adverse effects | RCT plus crossover; 18 |
| Backonja et al. (15) | Diabetic neuralgia | 165 | 53 ± 10.32 | 60 | 11.61 ± 9.15 | Gabapentin: 900 mg/day for the first week, increased to 3,600 mg/day from the fourth week | Identical placebo | Mean sleep interference scorec; adverse effect | RCT; 8 |
| Arnold et al. (14) | Fibromyalgia | 150 | 48.25 ± 11.22 | 90 | ≥0.5 | Gabapentin: 300 mg before bedtime at the first week, increased to 600 mg twice a day plus 1,200 mg before bedtime from the sixth week | Identical placebo | Medical outcomes study sleep problems index score (45); adverse effects | RCT; 12 |
| Winkelman et al. (36) | RLS | 272 | 52.0 ± 12.7 | 41.98 | NR | Gabapentin enacarbil: 600 mg/day initially, increased to 1,200 mg/day from the fourth day to the end of the first 4 weeks, followed by another 4-week placebo treatment phase after a 7-day dose-decreasing period and a 7-day washout period | 4 weeks of identical placebo, followed by 4 weeks of gabapentin enacarbil treatment after 2 weeks of washout | Polysomnography parameters; subjective post-sleep diary; tolerability assessments | RCT plus crossover; 8 |
| Vieta et al. (33) | Bipolar disorder | 25 | 46.87 ± 14.74 | 28 | 18.79 ± 10.90 | Gabapentin: 1,200 mg/day initially, adjusted to 900 mg/day within 1 week according to the symptoms and patient tolerance | Identical placebo | Pittsburgh sleep quality index global score (44); adverse effects | RCT; 54 |
| Pinkerton et al. (28) | Hot flashes in menopause | 593 | 54 ± 6.05 | 0 | ≥2 | Gabapentin: 600 mg/day initially, increased to 1,800 mg/day (600 mg with breakfast and 1,200 mg with the evening meal) from the seventh day | Identical placebo | Mean sleep interference scorec; adverse effects | RCT; 24 |
| Wallace et al. (34) | Postherpetic neuralgia | 400 | 66.67 ± 12.55 | 52 | ≥0.25 | Gabapentin: 1,800 mg at night for Group 1 and 600 mg in the morning and 1,200 mg at night for Group 2 | Identical placebo | Mean sleep interference scorec; adverse effects | RCT; 10 |
| Irving et al. (22) | Postherpetic neuralgia | 158 | 69.37 ± 11.59 | 46.84 | ≥0.25 | Gabapentin: 1,800 mg at night for Group 1 and 600 mg in the morning and 1,200 mg at night for Group 2 | Identical placebo | Mean sleep interference scorec; adverse effects | RCT; 4 |
| Lee et al. (26) | RLS | 322 | 48.95 ± 12.56 | 58.60 | 15.56 ± 12.09 | Gabapentin enacarbil: 600 mg/day for Group 1 and 1,200 mg/day (once daily at 5:00 p.m. for Group 2) | Identical placebo | Pittsburgh sleep diary, post-sleep questionnaire; adverse effects | RCT; 12 |
| Kushida et al. (23) | RLS | 221 | 51.12 ± 12.80 | 40.27 | 14.07 ± 13.78 | Gabapentin(XP13512) 1,200 mg once daily at 5:00 p.m. | Identical placebo | Medical outcomes study sleep problems index score (45); post-sleep questionnaire; Pittsburgh Sleep Diary (46); adverse effects | RCT; 12 |
| Kushida et al. (23) | RLS | 76 | 50.1 ± 13.2 | 42.11 | 14.30 ± 14.09 | Gabapentin(XP13512) 1,800 mg/day during Period 1 followed by placebo during Period 2 | Placebo during Period 1, followed by Gabapentin (XP13512) 1,800 mg/day during Period 2 | Polysomnography parameters; adverse effects | RCT plus crossover; 4 |
| Walters et al. (35) | RLS | 95 | 50.44 ± 11.17 | 37.89 | 16.0 ± 13.11 | Gabapentin enacarbil: the dose was 600 mg/day for Group 1 and 1,200 mg/day (once a day at 5:00 p.m.) for Group 2 | Identical placebo | Post-sleep questionnaire; adverse effects | RCT; 2 |
| Backonja et al. (16) | Postherpetic neuralgia | 102 | 64.47 ± 12.47 | 45.54 | 3.27 ± 4.11 | Gabapentin enacarbil: 1,200 mg twice daily | Identical placebo | Mean sleep interference scorec; adverse effects | RCT; 2 |
| Sang et al. (32) | Postherpetic neuralgia | 450 | 65.61 ± 12.22 | 37.39 | 1.68 ± 1.17 | Gastroretentive gabapentin: 1,800 mg/day | Identical placebo | Mean sleep interference scorec; adverse effects | RCT; 11 |
| Sandercock et al. (31) | Diabetic neuralgia | 147 | 58.68 ± 8.24 | 55.10 | 10.14 ± 8.72 | Gastroretentive gabapentin: 3,000 mg at night for Group 1 and 1,200 mg in the morning and 1,800 mg at night for Group 2 | Identical placebo | Mean sleep interference scorec; adverse effects | RCT; 4 |
| Bogan et al. (17) | RLS | 190 | 51.45 ± 11.90 | 59.07 | 14.01 ± 14.13 | Gabapentin enacarbil: 1,200 mg once daily | Gabapentin enacarbil at a dose of 600 mg and one tablet of placebo during the first 2 weeks, two placebo tablets from the third week | Post-sleep questionnaire (23); medical Outcomes Study Sleep Scale; kilogram effects | RCT; 12 (excluding the open-label period) |
| Yurcheshen et al. (37) | Hot flashes in menopause | 59 | 52.85 ± 3.34 | 0 | 4.17 ± 3.77 | Gabapentin: 300 mg three times daily | Identical placebo | Pittsburgh Sleep Quality Index global score (44); adverse effects | RCT; 12 |
Characteristics of the included studies.
RCT, randomized controlled trial; RLS, restless legs syndrome; NR, not reported.
aResults are shown as the mean ± SD.
bResults are shown as the median (interquartile ranges).
cThe range is 0–10, with 0 = no sleep interference and 10 = worst possible sleep interference.
dResults are shown as the mean (range).
eThe range is 0–100, with 0 = no sleep interference and 100 = worst possible sleep interference.
Quality Assessment
There were seven trials (14, 16, 18, 19, 32, 33, 41) (26.92%) with random sequence generation (14, 16, 18, 19, 22, 32, 33, 41) (30.77%) with allocation concealment, eight trials (14, 16, 18, 19, 22, 32, 33, 41) (30.77%) with blinding of participants, and three trials (16, 32, 41) (11.54%) with blinding of personnel treating the patients and outcome assessors. Except for the 26 trials above that had unclear risks, the trials included in this study had low risks of bias (Figures S1 and S2 in Supplementary Material).
Efficacy
A pooled analysis of eight trials (21, 23, 25–27, 29, 40, 41) demonstrated that other than some indicators in three trials (26, 40, 41), gabapentin showed a treatment efficacy superior to that of the placebos in all trials (Table 2). Regarding multiple subjective and objective sleep indices, the meta-analyses indicated that, except for Composite Endpoint 3 (13, 18, 33, 35) [SMD = 0.09, 95% confidence interval (CI): −0.05–0.22], Composite Endpoint 1 (23, 24, 26, 36, 37), Composite Endpoint 2 (16, 19, 22–24, 26, 28, 30–32, 34, 35, 37), Composite Endpoint 4 (14, 15, 18, 19, 30, 33, 35), Composite Endpoint 5 (17, 26), and Composite Endpoint 6 (17, 26) confirmed that gabapentin’s treatment efficacy was superior to that of the placebos (Figures 2 and 3).
Table 2
| Trials | Endpoints |
|---|---|
| Kushida et al. (23) | Compared with the placebo group, the gabapentin group showed significant improvement in sleep quality (P < 0.001), next-day functioning (P < 0.001), number of nighttime awakenings caused by RLS symptoms (P = 0.043), and number of hours awake due to RLS symptoms (P = 0.019) after 12 weeks of treatment; the gabapentin group had a significantly prolonged total sleep time after 2 weeks of treatment (P = 0.003), but there was no statistically significant difference between the two groups after 12 weeks of treatment (P = 0.187) |
| Lee et al. (26) | Compared with the placebo group, the patients who received the treatment at a dose of 600 mg had a significantly shortened average daily wake time after sleep onset at all studied time points (P < 0.05) with no increase in their total sleep time (P > 0.05) |
| Hahn et al. (21) | Compared with the placebo group, the gabapentin group showed a significantly improved mean sleep interference score (P < 0.05) |
| Lal et al. (25) | Compared with the placebo group, the gabapentin group showed a significant improvement in all sleep indices (an excellent overall quality of sleep, an excellent ability to function, fewer nights with RLS symptoms, fewer awakenings during the night, 0 or less than 1 h awake per night because of RLS symptoms) |
| Mason et al. (27) | Compared with the placebo group, the gabapentin group (1,800 mg) had a significantly improved Pittsburgh Sleep Quality Index total score (P < 0.001) |
| Rice et al. (29) | Compared with the placebo group, the gabapentin group (1,800 and 2,400 mg) had a significantly improved mean sleep interference score (P < 0.01) |
| Bone et al. (40) | In terms of the mean sleep interference score, neither the gabapentin group nor the placebo group showed a statistically significant difference (P > 0.05) |
| Brower et al. (41) | Compared with before treatment, the gabapentin group and the placebo group showed improvement in the subjective indices (Sleep Problems Questionnaire, sleep diaries) and the objective indices (polysomnography parameters: sleep onset latency, sleep efficiency, wake time after sleep onset, total sleep time, percentage of sleep spent in Stage 1, percentage of sleep spent in Stage 2, percentage of slow-wave sleep, and percentage of rapid eye movement sleep), but there was no statistically significant difference between the two groups (P > 0.05) |
Efficacy comparison of gabapentin and placebos.
Figure 2
Figure 3
Tolerability
All of the trials reported mild-to-moderate adverse effects. The moderate adverse effects occurred primarily during the dose-increasing phase and significantly decreased in frequency afterward. Drowsiness, dizziness, and weakness were the most frequently reported effects. These discomforts were tolerable for the majority of patients but resulted in drug withdrawal in a portion of patients. A meta-analysis of 20 trials (7, 14–17, 19, 21, 22, 25–28, 32–37) showed that for adverse events that were possibly or probably related to the study drug and could lead to treatment discontinuation and drug withdrawal, the gabapentin group had a 1.45-times higher risk than the placebo group (RR = 1.38; 95% CI: 1.08–1.76; Figure 3); For adverse events that were possibly or probably related to the study drug and could lead to treatment discontinuation and drug withdrawal, the incidences in the gabapentin group and the placebo group were 8.19 and 5.37% (P < 0.001), respectively. Sixteen trials (14, 17, 19, 21, 22, 25–29, 31–34, 36) reported serious adverse effects. However, other than one case of headache (34), one case of serious dizziness and drowsiness (21), and one case of vision disturbance (19), no serious adverse effects were associated with the use of gabapentin. No serious adverse events associated with the use of placebos were found.
GRADE Classification
For the GRADE classifications of evidence quality, the high, moderate, low, and extremely low were 0, 3, 3, and 0, respectively (Table 3).
Table 3
| Outcomes | Illustrative comparative risksa (95% CI) | Relative effect (95% CI) | No of participants (studies) | Quality of the evidence [Grading of Recommendations Assessment, Development and Evaluation (GRADE)] | |
|---|---|---|---|---|---|
| Assumed risk | Corresponding risk | ||||
| Placebo | Gabapentin | ||||
| Composite Endpoint 1 follow-up: mean 9.67 weeks | The mean Composite Endpoint 1 in the intervention groups was 0.53 SDs higher (0.41–0.66 higher) | 2,797 (5 studies) | ⊕⊕⊕⊖moderateb | ||
| Composite Endpoint 2 follow-up: mean 10.28 weeks | The mean Composite Endpoint 2 in the intervention groups was 0.45 SDs lower (0.61–0.3 lower) | 5,841 (13 studies) | ⊕⊕⊖⊖lowb,c | ||
| Composite Endpoint 4 follow-up: mean 8.09 weeks | The mean Composite Endpoint 4 in the intervention groups was 0.53 SDs lower (0.69–0.36 lower) | 1,501 (7 studies) | ⊕⊕⊖⊖lowb,c | ||
| Composite Endpoint 5 follow-up: mean 10.97 weeks | Study population 309 per 1,000 Moderate | 526 per 1,000 (383–798) | RR 1.7 (1.24–2.58) | 2,910 (3 studies) | ⊕⊕⊖⊖lowb,c |
| Composite Endpoint 6 follow-up: mean 10.97 weeks | Study population 122 per 1,000 Moderate | 59 per 1,000 (39–88) | RR 0.48 (0.32–0.72) | 2,910 (3 studies) | ⊕⊕⊕⊖moderatec |
| Composite Endpoint 7 follow-up: mean 11.60 weeks | Study population 54 per 1,000Moderate | 74 per 1,000 (58–94) | RR 1.38 (1.08–1.76) | 4,097 (20 studies) | ⊕⊕⊕⊖moderatec |
Summary of the ratings regarding the quality of evidence.
aThe basis for the assumed risk (e.g., the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI, confidence interval; RR, risk ratio.
GRADE Working Group grades of evidence.
High quality: further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: we are very uncertain about the estimate.
bThe differences exist among the trial’s objects.
cThe variation in point estimates among different trials was relatively large, and the heterogeneity test showed results of P < 0.10 and I2 > 40%.
Sensitivity Analysis
The sensitivity analysis indicated that, for Composite Endpoint 1, the removal of any one trial led to a lower limit of the CI of SMD that was higher than 0; for Composite Endpoint 2 and Composite Endpoint 4, the removal of any one trial led to an upper limit of the CI of SMD that was lower than 0; for Composite Endpoint 5 and Composite Endpoint 7, the removal of any one trial led to a lower limit of the CI of the RR that was higher than 1; for Composite Endpoint 6, the removal of any one trial led to the lower limit of the CI of the RR that was lower than 1 (Figures S3–S8 in Supplementary Material). The above results suggest that the results for these endpoints were robust and had a low sensitivity.
Publication Bias
The P values of all endpoints derived from the Egger test were greater than 0.05, indicating there was no publication bias (Table 4).
Table 4
| Results | Composite Endpoint 1 | Composite Endpoint 2 | Composite Endpoint 4 | Composite Endpoint 5 | Composite Endpoint 6 | Composite Endpoint 7 |
|---|---|---|---|---|---|---|
| P-value | 0.241 | 0.053 | 0.063 | 0.138 | 0.567 | 0.336 |
| 95% CI | −8.18–3.04 | −0.12–14.04 | −18.67–0.69 | −11.28–23.83 | −32.97–29.02 | −0.51–1.43 |
Results of the Egger test.
CI, confidence interval.
Discussion
This study revealed that without consideration of the type of sleep outcomes, gabapentin was significantly superior to placebos for the treatment for sleep disorders secondary to RLS, neuropathic pain, alcohol dependence, hot flashes in menopause, fibromyalgia, phantom limb pain, HIV-associated sensory neuropathies, and bipolar disorder. However, with an average dose of approximately 1,800 mg/day, gabapentin had a higher risk of treatment discontinuation and drug withdrawal compared with placebo.
The above conclusion was drawn from an extensive summary of trials involving various primary diseases. Only a small portion of these trials reported the baseline sleep status (14, 18, 21, 26, 27, 36, 37, 41), and none of these trials reported the sleep status prior to the disease. Because it was impossible to distinguish absolutely true, partially true, and false sleep disturbance, we could not exclude the contribution of false sleep disturbance to the final treatment efficacy in patients with medical illness. However, it is worth noting that more than 90% of the patients in these trials had an average disease course of 6.23 (±9.76) years. In terms of the psychological aspects of insomnia, the intention to fall sleep often becomes a driving factor of sleep difficulty (47) and worries about being sleepless often cause early awakening or anxiety (48), particularly among patients who are prone to excessive worry or over thinking. Without timely correction, one episode of sleep difficulty can easily induce a second episode in patients with related psychological traits, and as a result, ongoing sleep difficulties ultimately lead to a chronic sleep disorder. Some researchers believe that the initiating event does not significantly affect the progression of chronic sleep disorders (49) and that chronic sleep disorders are not closely associated with primary disease and thus do not improve with the improvement of the primary disease. In other words, during the chronic course of the abovementioned primary diseases, false sleep disturbance might have transformed into true or partially true sleep disturbance in patients with medical illness for the majority of the sample pool. Thus, we believe the existence of false sleep disturbance in medical illness would not significantly affect the results of the efficacy analysis, and the improvement of sleep disorders can be attributed to the efficacy of gabapentin treatment. The following experimental evidence supports this deduction: gabapentin can shorten sleep latency (36), reduce awakenings (12, 26, 35, 36), reduce fast-wave sleep (23), enhance slow-wave sleep (9–12, 18, 36), prolong the total sleep time (18, 23, 36), increase sleep efficiency (12, 18, 36), and improve the quality of sleep (17, 23, 35, 36). In fact, because of its sedative effect in various diseases, gabapentin has been clinically used as a hypnotic (48). Nevertheless, its efficacy for primary sleep disorders remains to be verified by randomized controlled trials, and the optimal dosage that is effective and tolerable in most patients needs to be identified.
It is necessary to emphasize that despite its insignificant impact on the progression of sleep disorders, the initial sleep difficulty can induce the recurrence of disease (49). In other words, the complete cure of sleep disorders requires a complete removal of the initiating stimulus. Therefore, the use of gabapentin in the abovementioned diseases can “kill two birds with one stone.”
Moreover, it is worth noting that pooled statistics were used with the basic premise of analyzing the efficacy of gabapentin. In this study, we introduced the concept of “composite endpoints” to pool sleep-outcome data that had similar significance and consistent direction. In a broad sense, this research method is in accordance with the basic principle of meta-analysis (39).
Research Significance
Through a systematic review and meta-analysis, this study for the first time systematically evaluated the clinical value of gabapentin for the treatment of sleep disorders. Used as a starting point, this study could inspire more researchers to conduct in-depth research on this topic.
Study Limitations
Because of the difficulty of distinguishing false sleep disturbance from true ones in patients with medical illness, we were unable to exclude their contribution to the treatment efficacy. In addition, because of the limitations of the original trials, we were unable to conduct a meta-analysis of individual sleep outcomes and analyses related to treatment dose and timing or patient gender.
Conclusion
This is the first study to systematically evaluate the clinical value of gabapentin for the treatment of sleep disorders. Regardless the type of sleep outcomes, gabapentin showed stable efficacy in the treatment for sleep disturbance in patients with medical illness with a relatively high risk of treatment discontinuation and drug withdrawal when used at an average dose of approximately 1,800 mg/day. Because the adverse events often occurred during the dose-increasing phase, and the dose was high, reducing the dose-increasing speed and lowering the dosage of gabapentin might reduce the risk. In addition, it would be ideal if our conclusions could be further verified in patients with primary sleep disorders.
Statements
Author contributions
All authors contributed equally to this work.
Funding
. Y-FW was support by the foundation of Hubei province public welfare science and technology research project (2012DCA12006), and LD was supported by the foundation of health and family planning commission of Hubei province (WJ2015MB222). Role of the Funding Source: The research results and conclusions were not affected by the financial support.
Acknowledgments
We greatly appreciate the help of Dr. Hui Nie from Durham of North Carolina, USA with the translation of this manuscript. Also thanks to Dr Hui Hui Wu and Dr Shao Hua Cheng of Taihe Hospital for their help.
Conflict of interest
The authors report no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Supplementary material
The Supplementary Material for this article can be found online at http://journal.frontiersin.org/article/10.3389/fneur.2017.00316/full#supplementary-material.
References
1
LaugsandLEStrandLBPlatouCVattenLJJanszkyI. Insomnia and the risk of incident heart failure: a population study. Eur Heart J (2014) 35:1382–93.10.1093/eurheartj/eht019
2
ParthasarathySVasquezMMHalonenMBootzinRQuanSFMartinezFDet alPersistent insomnia is associated with mortality risk. Am J Med (2015) 128:268.e–75.e.10.1016/j.amjmed.2014.10.015
3
SofiFCesariFCasiniAMacchiCAbbateRGensiniGF. Insomnia and risk of cardiovascular disease: a meta-analysis. Eur J Prev Cardiol (2014) 21:57–64.10.1177/2047487312460020
4
DaleyMMorinCMLeBlancMGregoireJPSavardJ. The economic burden of insomnia: direct and indirect costs for individuals with insomnia syndrome, insomnia symptoms, and good sleepers. Sleep (2009) 32:55–64.10.1016/j.sleep.2008.04.005
5
HillmanDRLackLC. Public health implications of sleep loss: the community burden. Med J Aust (2013) 199:S7–10.10.5694/mja13.10620
6
KuriyamaAHondaMHayashinoY. Ramelteon for the treatment of insomnia in adults: a systematic review and meta-analysis. Sleep Med (2014) 15:385–92.10.1016/j.sleep.2013.11.788
7
WinklerAAuerCDoeringBKRiefW. Drug treatment of primary insomnia: a meta-analysis of polysomnographic randomized controlled trials. CNS Drugs (2014) 28:799–816.10.1007/s40263-014-0198-7
8
LanaBSchlickBMartinSPrattWSPageKMGoncalvesLet alDifferential upregulation in DRG neurons of an alpha2delta-1 splice variant with a lower affinity for gabapentin after peripheral sensory nerve injury. Pain (2014) 155:522–33.10.1016/j.pain.2013.12.001
9
Foldvary-SchaeferNDe Leon SanchezIKarafaMMaschaEDinnerDMorrisHH. Gabapentin increases slow-wave sleep in normal adults. Epilepsia (2002) 43:1493–7.10.1046/j.1528-1157.2002.21002.x
10
JainSVGlauserTA. Effects of epilepsy treatments on sleep architecture and daytime sleepiness: an evidence-based review of objective sleep metrics. Epilepsia (2014) 55:26–37.10.1111/epi.12597
11
LegrosBBazilCW. Effects of antiepileptic drugs on sleep architecture: a pilot study. Sleep Med (2003) 4:51–5.10.1016/s1389-9457(02)00217-4
12
LoHSYangCMLoHGLeeCYTingHTzangBS. Treatment effects of gabapentin for primary insomnia. Clin Neuropharmacol (2010) 33:84–90.10.1097/WNF.0b013e3181cda242
13
AntonRFMyrickHWrightTMLathamPKBarosAMWaidLRet alGabapentin combined with naltrexone for the treatment of alcohol dependence. Am J Psychiatry (2011) 168:709–17.10.1176/appi.ajp.2011.10101436
14
ArnoldLMGoldenbergDLStanfordSBLalondeJKSandhuHSKeckPEJret alGabapentin in the treatment of fibromyalgia: a randomized, double-blind, placebo-controlled, multicenter trial. Arthritis Rheum (2007) 56:1336–44.10.1002/art.22457
15
BackonjaMBeydounAEdwardsKRSchwartzSLFonsecaVHesMet alGabapentin for the symptomatic treatment of painful neuropathy in patients with diabetes mellitus: a randomized controlled trial. JAMA (1998) 280:1831–6.10.1001/jama.280.21.1831
16
BackonjaMMCanafaxDMCundyKC. Efficacy of gabapentin enacarbil vs placebo in patients with postherpetic neuralgia and a pharmacokinetic comparison with oral gabapentin. Pain Med (2011) 12:1098–108.10.1111/j.1526-4637.2011.01139.x
17
BoganRKBornemannMAKushidaCATranPVBarrettRW. Long-term maintenance treatment of restless legs syndrome with gabapentin enacarbil: a randomized controlled study. Mayo Clin Proc (2010) 85:512–21.10.4065/mcp.2009.0700
18
Garcia-BorregueroDLarrosaOde la LlaveYVergerKMasramonXHernandezG. Treatment of restless legs syndrome with gabapentin: a double-blind, cross-over study. Neurology (2002) 59:1573–9.10.1212/WNL.59.10.1573
19
GordhTEStubhaugAJensenTSArnèrSBiberBBoivieJet alGabapentin in traumatic nerve injury pain: a randomized, double-blind, placebo-controlled, cross-over, multi-center study. Pain (2008) 138:255–66.10.1016/j.pain.2007.12.011
20
GuyattGHOxmanADSchunemannHJTugwellPKnottnerusA. GRADE guidelines: a new series of articles in the Journal of Clinical Epidemiology. J Clin Epidemiol (2011) 64:380–2.10.1016/j.jclinepi.2010.09.011
21
HahnKArendtGBraunJSvon GiesenHJHusstedtIWMaschkeMet alA placebo-controlled trial of gabapentin for painful HIV-associated sensory neuropathies. J Neurol (2004) 251:1260–6.10.1007/s00415-004-0529-6
22
IrvingGJensenMCramerMWuJChiangYKTarkMet alEfficacy and tolerability of gastric-retentive gabapentin for the treatment of postherpetic neuralgia: results of a double-blind, randomized, placebo-controlled clinical trial. Clin J Pain (2009) 25:185–92.10.1097/AJP.0b013e3181934276
23
KushidaCABeckerPMEllenbogenALCanafaxDMBarrettRW. Randomized, double-blind, placebo-controlled study of XP13512/GSK1838262 in patients with RLS. Neurology (2009) 72:439–46.10.1212/01.wnl.0000341770.91926.cc
24
KushidaCAWaltersASBeckerPTheinSGPerkinsATRothTet alA randomized, double-blind, placebo-controlled, crossover study of XP13512/GSK1838262 in the treatment of patients with primary restless legs syndrome. Sleep (2009) 32:159–68.10.1093/sleep/32.2.159
25
LalREllenbogenAChenDZomorodiKAtluriHLuoWet alA randomized, double-blind, placebo-controlled, dose-response study to assess the pharmacokinetics, efficacy, and safety of gabapentin enacarbil in subjects with restless legs syndrome. Clin Neuropharmacol (2012) 35:165–73.10.1097/WNF.0b013e318259eac8
26
LeeDOZimanRBPerkinsATPocetaJSWaltersASBarrettRW. A randomized, double-blind, placebo-controlled study to assess the efficacy and tolerability of gabapentin enacarbil in subjects with restless legs syndrome. J Clin Sleep Med (2011) 7:282–92.10.5664/JCSM.1074
27
MasonBJQuelloSGoodellVShadanFKyleMBegovicA. Gabapentin treatment for alcohol dependence: a randomized clinical trial. JAMA Intern Med (2014) 174:70–7.10.1001/jamainternmed.2013.11950
28
PinkertonJVKaganRPortmanDSathyanarayanaRSweeneyM. Phase 3 randomized controlled study of gastroretentive gabapentin for the treatment of moderate-to-severe hot flashes in menopause. Menopause (2014) 21:567–73.10.1097/GME.0b013e3182a7c073
29
RiceASMatonS. Gabapentin in postherpetic neuralgia: a randomised, double blind, placebo controlled study. Pain (2001) 94:215–24.10.1016/S0304-3959(01)00407-9
30
RowbothamMHardenNStaceyBBernsteinPMagnus-MillerL. Gabapentin for the treatment of postherpetic neuralgia: a randomized controlled trial. JAMA (1998) 280:1837–42.10.1001/jama.280.21.1837
31
SandercockDCramerMBitonVCowlesVE. A gastroretentive gabapentin formulation for the treatment of painful diabetic peripheral neuropathy: efficacy and tolerability in a double-blind, randomized, controlled clinical trial. Diabetes Res Clin Pract (2012) 97:438–45.10.1016/j.diabres.2012.03.010
32
SangCNSathyanarayanaRSweeneyM. Gastroretentive gabapentin (G-GR) formulation reduces intensity of pain associated with postherpetic neuralgia (PHN). Clin J Pain (2013) 29:281–8.10.1097/AJP.0b013e318258993e
33
VietaEManuel GoikoleaJMartínez-AránAComesMVergerKMasramonXet alA double-blind, randomized, placebo-controlled, prophylaxis study of adjunctive gabapentin for bipolar disorder. J Clin Psychiatry (2006) 67:473–7.10.4088/JCP.v67n0320
34
WallaceMSIrvingGCowlesVE. Gabapentin extended-release tablets for the treatment of patients with postherpetic neuralgia: a randomized, double-blind, placebo-controlled, multicentre study. Clin Drug Investig (2010) 30:765–76.10.2165/11539520-000000000-00000
35
WaltersASOndoWGKushidaCABeckerPMEllenbogenALCanafaxDMet alGabapentin enacarbil in restless legs syndrome: a phase 2b, 2-week, randomized, double-blind, placebo-controlled trial. Clin Neuropharmacol (2009) 32:311–20.10.1097/WNF.0b013e3181b3ab16
36
WinkelmanJWBoganRKSchmidtMHHudsonJDDeRossettSEHill-ZabalaCE. Randomized polysomnography study of gabapentin enacarbil in subjects with restless legs syndrome. Mov Disord (2011) 26:2065–72.10.1002/mds.23771
37
YurcheshenMEGuttusoTJrMcDermottMHollowayRGPerlisM. Effects of gabapentin on sleep in menopausal women with hot flashes as measured by a Pittsburgh Sleep Quality Index factor scoring model. J Womens Health (Larchmt) (2009) 18:1355–60.10.1089/jwh.2008.1257
38
LiberatiAAltmanDGTetzlaffJMulrowCGøtzschePCIoannidisJPet alThe PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. PLoS Med (2009) 6:e1000100.10.1371/journal.pmed.1000100
39
HigginsJPGreenS. The Cochrane Handbook for Systematic Reviews of Interventions 5.1.0. (updated march 2011) The Cochrane Collaboration Website. (2016). Available from: http://handbook.cochrane.org
40
BoneMCritchleyPBuggyDJ. Gabapentin in postamputation phantom limb pain: a randomized, double-blind, placebo-controlled, cross-over study. Reg Anesth Pain Med (2002) 27:481–6.10.1097/00115550-200209000-00007
41
BrowerKJMyra KimHStrobbeSKaram-HageMAConsensFZuckerRA. A randomized double-blind pilot trial of gabapentin versus placebo to treat alcohol dependence and comorbid insomnia. Alcohol Clin Exp Res (2008) 32:1429–38.10.1111/j.1530-0277.2008.00706.x
42
BastienCHVallieresAMorinCM. Validation of the Insomnia Severity Index as an outcome measure for insomnia research. Sleep Med (2001) 2:297–307.10.1016/S1389-9457(00)00065-4
43
JohnsMW. A new method for measuring daytime sleepiness: the Epworth sleepiness scale. Sleep (1991) 14:540–5.10.1093/sleep/14.6.540
44
BuysseDJReynoldsCFIIIMonkTHBermanSRKupferDJ. The Pittsburgh Sleep Quality Index: a new instrument for psychiatric practice and research. Psychiatry Res (1989) 28:193–213.10.1016/0165-1781(89)90047-4
45
HaysRDStewartAL. Sleep measures. In: StewartALWareJE, editors. Measuring Functioning and Well-Being. Durham, NC: Duke University Press (1992). p. 232–59.
46
MonkTHReynoldsCFKupferDJBuysseDJCoblePAHayesAJet alThe Pittsburgh Sleep Diary. J Sleep Res (1994) 3:111–20.10.1111/j.1365-2869.1994.tb00114.x
47
ZhaoZX. Sleep disorders. 5th ed. In: WangWZLuoZM, editors. Neurology. Beijing: People’s Medical Publishing House (2004). p. 256–64.
48
FischerJDogasZBassettiCLBergSGroteLJennumPet alStandard procedures for adults in accredited sleep medicine centres in Europe. J Sleep Res (2012) 21:357–68.10.1111/j.1365-2869.2011.00987.x
49
ZhangXHHanFZhangYWangLX. Principles and Practice of Sleep Medicine. 5th ed. Beijing: People’s Medical Publishing House (2010). 457,586,590 p.
Summary
Keywords
sleep disturbance, gabapentin, efficacy, tolerability, meta-analysis
Citation
Liu GJ, Karim MR, Xu LL, Wang SL, Yang C, Ding L and Wang Y-F (2017) Efficacy and Tolerability of Gabapentin in Adults with Sleep Disturbance in Medical Illness: A Systematic Review and Meta-analysis. Front. Neurol. 8:316. doi: 10.3389/fneur.2017.00316
Received
27 April 2017
Accepted
16 June 2017
Published
14 July 2017
Volume
8 - 2017
Edited by
Con Stough, Swinburne University of Technology, Australia
Reviewed by
Christine Dugovic, Janssen Research & Development, L.L.C., United States; Robert L. Barkin, Rush University Medical Center/Northshore University Health System, United States
Updates
Copyright
© 2017 Liu, Karim, Xu, Wang, Yang, Ding and Wang.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Yun-Fu Wang, wyfymc@sina.com
Specialty section: This article was submitted to Neuropharmacology, a section of the journal Frontiers in Neurology
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