Sleep-disordered breathing is frequently associated with idiopathic normal pressure hydrocephalus but not other types of hydrocephalus
Research output: Contribution to journal › Journal article › Research › peer-review
Standard
Sleep-disordered breathing is frequently associated with idiopathic normal pressure hydrocephalus but not other types of hydrocephalus. / Riedel, Casper Schwartz; Milan, Joachim Birch; Juhler, Marianne; Jennum, Poul.
In: Sleep, Vol. 45, No. 3, zsab265, 2022.Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
APA
Vancouver
Author
Bibtex
}
RIS
TY - JOUR
T1 - Sleep-disordered breathing is frequently associated with idiopathic normal pressure hydrocephalus but not other types of hydrocephalus
AU - Riedel, Casper Schwartz
AU - Milan, Joachim Birch
AU - Juhler, Marianne
AU - Jennum, Poul
N1 - Funding Information: The authors gratefully acknowledge support in the form of research grants from the Lundbeck Foundation (R211-2015-2937), the Alzheimer's Research Fund, the IMK Almene Fund, and the Novo Nordisk Foundation (NNF17OC0024718).
PY - 2022
Y1 - 2022
N2 - Study Objectives: Previous studies have shown sleep-disordered breathing (SDB) to be highly prevalent in patients with idiopathic normal pressure hydrocephalus (iNPH). The current study aimed to estimate and compare the prevalence of SDB in patients with different types of hydrocephalus and test if SDB was associated with changed CO2. Methods: We investigated the prevalence of SDB in a prospective cohort of 48 hydrocephalus patients with nocturnal polysomnography (PSG). Twenty-three of the patients also had simultaneous CO2 measurements. Results: The prevalence of SDB was high in patients with iNPH, with moderate-to-severe SDB in 21/22 (96%) of the patients and an apnea-hypopnea index (AHI) of 43.5 (95% CI 33.8-52.2). Patients with pediatric-onset hydrocephalus had moderate-to-severe SDB in 7/16 (44%), with an AHI of 16.1 (95% CI 8.16-23.8). Except for one patient, all patients with adult-onset obstructive hydrocephalus (9/10) had normal respiration or mild SDB with an AHI of 8.4 (95% CI 5.5-10.5). None of the 23 patients measured with CO2 had elevated CO2 associated with SDB and had normal CO2 during sleep, with 40.8 ± 5.5 mmHg, 42.7 ± 4.1 mmHg, 34.5-45.8 mmHg for patients with iNPH, pediatric-onset, and adult-onset, respectively. Conclusion: We found a high prevalence of SDB in patients with iNPH, confirming previous findings. We extended this with the finding that the prevalence of SDB in patients with other types of hydrocephalus is not significantly different from that in the general population. Additionally, we did not find elevations of CO2 associated with SDB or CO2 retention during sleep. Statement of Significance This study highlights the possible role of sleep-disordered breathing (SDB) in idiopathic normal pressure hydrocephalus (iNPH). Acknowledging, diagnosing, and treating SDB in patients with iNPH could be critical in alleviating the cognitive symptoms, alongside the standard surgical methods used to treat iNPH today. Surgical treatment with a shunt is the only treatment option today, but this treatment is far from optimal. Even after treatment, these patients often have rapid worsening of their symptoms and many complications, leading to additional surgery; thus, additional or alternative treatments are essential. Furthermore, our results suggest that SDB is not caused by hydrocephalus but rather that SDB can play a role in the enigmatic pathogenesis of iNPH and, over time, maybe damage the brain if left untreated.
AB - Study Objectives: Previous studies have shown sleep-disordered breathing (SDB) to be highly prevalent in patients with idiopathic normal pressure hydrocephalus (iNPH). The current study aimed to estimate and compare the prevalence of SDB in patients with different types of hydrocephalus and test if SDB was associated with changed CO2. Methods: We investigated the prevalence of SDB in a prospective cohort of 48 hydrocephalus patients with nocturnal polysomnography (PSG). Twenty-three of the patients also had simultaneous CO2 measurements. Results: The prevalence of SDB was high in patients with iNPH, with moderate-to-severe SDB in 21/22 (96%) of the patients and an apnea-hypopnea index (AHI) of 43.5 (95% CI 33.8-52.2). Patients with pediatric-onset hydrocephalus had moderate-to-severe SDB in 7/16 (44%), with an AHI of 16.1 (95% CI 8.16-23.8). Except for one patient, all patients with adult-onset obstructive hydrocephalus (9/10) had normal respiration or mild SDB with an AHI of 8.4 (95% CI 5.5-10.5). None of the 23 patients measured with CO2 had elevated CO2 associated with SDB and had normal CO2 during sleep, with 40.8 ± 5.5 mmHg, 42.7 ± 4.1 mmHg, 34.5-45.8 mmHg for patients with iNPH, pediatric-onset, and adult-onset, respectively. Conclusion: We found a high prevalence of SDB in patients with iNPH, confirming previous findings. We extended this with the finding that the prevalence of SDB in patients with other types of hydrocephalus is not significantly different from that in the general population. Additionally, we did not find elevations of CO2 associated with SDB or CO2 retention during sleep. Statement of Significance This study highlights the possible role of sleep-disordered breathing (SDB) in idiopathic normal pressure hydrocephalus (iNPH). Acknowledging, diagnosing, and treating SDB in patients with iNPH could be critical in alleviating the cognitive symptoms, alongside the standard surgical methods used to treat iNPH today. Surgical treatment with a shunt is the only treatment option today, but this treatment is far from optimal. Even after treatment, these patients often have rapid worsening of their symptoms and many complications, leading to additional surgery; thus, additional or alternative treatments are essential. Furthermore, our results suggest that SDB is not caused by hydrocephalus but rather that SDB can play a role in the enigmatic pathogenesis of iNPH and, over time, maybe damage the brain if left untreated.
KW - apnea-hypopnea index (AHI)
KW - CO
KW - hydrocephalus
KW - intracranial pressure (ICP)
KW - obstructive sleep apnea (OSA)
KW - polysomnography (PSG)
U2 - 10.1093/sleep/zsab265
DO - 10.1093/sleep/zsab265
M3 - Journal article
C2 - 34739077
AN - SCOPUS:85126389762
VL - 45
JO - Sleep (Online)
JF - Sleep (Online)
SN - 0161-8105
IS - 3
M1 - zsab265
ER -
ID: 310419671