6 research outputs found
Lip muscle training improves obstructive sleep apnea and objective sleep: a case report
The present study assessed the potential of lip muscle training for
improving sleep. A patient with heavy snoring, daytime sleepiness and dry mouth
underwent lip muscle training. Lip closure force LCFmax increased by 67.3% and LCFmin by
152% post-training. AHI decreased from 12.2 to 3.9 events/h by reducing hypopneic
episodes. TST, sleep stage N3 and REM sleep increased, and WASO, sleep stage N1, and AI
decreased. The patient switched from mouth to nose breathing during sleep and stopped
snoring. Improved LCF, by moving the tongue into the anterior-superior oral cavity, may
increase upper airway space and reduce the hypopnea index
Lip muscle training improves obstructive sleep apnea and objective sleep: a case report
The present study assessed the potential of lip muscle training for
improving sleep. A patient with heavy snoring, daytime sleepiness and dry mouth
underwent lip muscle training. Lip closure force LCFmax increased by 67.3% and LCFmin by
152% post-training. AHI decreased from 12.2 to 3.9 events/h by reducing hypopneic
episodes. TST, sleep stage N3 and REM sleep increased, and WASO, sleep stage N1, and AI
decreased. The patient switched from mouth to nose breathing during sleep and stopped
snoring. Improved LCF, by moving the tongue into the anterior-superior oral cavity, may
increase upper airway space and reduce the hypopnea index
Inhibitory effect on arterial injury-induced neointimal formation by adoptive B-cell transfer in Rag-1 knockout mice.
We investigated the effect of B-cell reconstitution in immune-deficient Rag-1 knockout (KO) mice subjected to arterial injury. After 21 days, injury induced a 4- to 5-fold increase in neointimal formation in Rag-1 KO mice fed normal chow compared with wild-type (WT) mice (0.020+/-0.0160 [n=8] versus 0.0049+/-0.0022 [n=8] mm(2), respectively; P<0.05) and in western-type diet-fed Rag-1 KO mice compared with WT mice (0.0312+/-0.0174 [n=7] versus 0.0050+/-0.0028 [n=6] mm(2), respectively; P<0.05). To investigate the role of B cells in response to injury, Rag-1 KO mice were reconstituted with B cells derived from the spleens of WT mice, with donors and recipients on the same diet. Reconstitution of Rag-1 KO mice with B cells from WT mice (both fed normal chow) reduced neointimal formation compared with the effect in unreconstituted Rag-1 KO mice (0.0076+/-0.0039 [n=9] versus 0.020+/-0.0160 [n=8] mm(2), respectively; P<0.05). Reconstitution of Rag-1 KO mice with B cells from WT mice (both fed a western diet) reduced neointimal formation compared the effect in Rag-1 KO mice (0.0087+/-0.0037 [n=8] versus 0.0312+/-0.0174 [n=7] mm(2), respectively; P<0.05). Injured carotid arteries from reconstituted Rag-1 KO mice had detectable IgM and IgG, indicating viable transfer of B cells. The results suggest that B cells modulate the response to arterial injury
Assessment of Screening for Nasal Obstruction among Sleep Dentistry Outpatients with Obstructive Sleep Apnea
Oral appliances (OA), a common treatment modality for obstructive sleep apnea (OSA), are not suitable for patients with nasal obstruction. Rhinomanometry, the gold standard technique to assess nasal airway resistance, is not readily available in sleep dentistry clinics. We demonstrate the use of a portable lightweight peak nasal inspiratory flow (PNIF) rate meter to objectively assess nasal airflow and utilized the Nasal Obstruction Symptom Evaluation (NOSE) scale to subjectively assess nasal obstruction in 97 patients with OSA and 105 healthy controls. We examined the correlations between the following variables between the groups: demographics, body mass index, PNIF, NOSE scale scores, apnea–hypopnea index (AHI), minimum SpO2 (SpO2min), Mallampati classification, and Epworth Sleepiness Scale (ESS) scores. Patients with OSA had significantly lower PNIF values and higher NOSE scores than controls. In the patient group, PNIF was not significantly correlated with AHI, SpO2min, Mallampati classification, or NOSE or ESS scores. Lower PNIF values and higher NOSE scores suggested impaired nasal airflow in the OSA group. As daytime PNIF measurement bears no relationship to AHI, this cannot be used alone in predicting the suitability of treatment for OSA with OA but can be used as an adjunct for making clinical decisions