Table 2 Obstructive Sleep Apnea severity parameters (some reported from previous study23), main sleep characteristics, and heart rate variability (HRV) at baseline, on placebo, and on active drugs combination (n = 16); HRV was assessed from EKG of nocturnal PSG during N2 sleep at baseline, on placebo, and on active drugs combination.

From: Impact of reboxetine plus oxybutynin treatment for obstructive sleep apnea on cardiovascular autonomic modulation

 

Baseline

Placebo

Reb-Oxy

p-value

Full night PSG

 AHI total, events/h

48.7 [34.8–56.6]

38.7 [29.0–47.8]

18.0 [12.5–21.4]

 < 0.01

 Hypoxic burden, %min/h

90.8 [69.5–154]

75.5 [68.1–168.0]

39.7 [25.4–55.3]

 < 0.01

 ODI 3%, events/h

42.7 [32.3–53.0]

36.8 [23.8–43.2]

31.4 [19.1–37.7]

0.03

 Total sleep time, min

329.5 [301.0–368.8]

323.5 [274.4–351.4]

321.8 [283.0–362.9]

0.50

 PLM index, events/h

0.0 [0.0–2.8]

0.0 [0.0–2.8]

0.5 [0.0–2.8]

0.81

 HR, bpm

65 [59.5–69]

65.6 [58.8–69.55]

69.35 [63.8–76.75]

0.02

HRV in N2 phase

 RMSSD, ms2

40.4 [17.5–51.6]

24.7 [17.6–43.1]

32.4 [25.4–51.6]

0.38

 pNN50

0.18 [0.01–0.32]

0.02 [0.001–0.18]

0.10 [0.03–0.35]

0.40

 HF, ms2

300.0 [90.7–748.4]

189.7 [85.6–527.2]

328.8 [181.5–887.9]

0.53

 LF, ms2

370.2 [136.9–1021.4]

222.8 [159.1–1099.7]

371.47 [227.8–614.94]

0.38

 LF/HF

2.4 [0.9–3.9]

1.3 [0.9–2.4]

1.1 [0.6–1.7]

0.46

 VLF, ms2

680.6 [341.1–2879.1]

504.4 [232.3–2095.3]

659.4 [434.4–885.6]

0.25

  1. reb–oxy = reboxetine plus oxybutynin; AHI = apnea–hypopnea index; ODI = oxygen desaturation index; PLM = periodic legs movements; HR = heart rate; SD = standard deviation; RMSSD = Root Mean Square of the Successive Differences; pNN50 = the proportion of number of pairs of successive NN (R-R) intervals that differ by more than 50 ms; HF = high frequency; LF = low frequency; VLF = very low frequency.
  2. Data are presented as median [interquartile] % changes are expressed as the median of percentage change. P values compare placebo versus reb-oxy.
  3. P-values are calculated by comparing the percentage changes from baseline observed in the placebo versus reb-oxy.