scholarly journals Increased Cellular Proliferation and Inflammatory Cytokines in Tonsils Derived From Children With Obstructive Sleep Apnea

2009 ◽  
Vol 66 (4) ◽  
pp. 423-428 ◽  
Author(s):  
Jinkwan Kim ◽  
Rakesh Bhattacharjee ◽  
Ehab Dayyat ◽  
Ayelet B Snow ◽  
Leila Kheirandish-Gozal ◽  
...  
2020 ◽  
Vol 21 (9) ◽  
pp. 3264
Author(s):  
Marcella Reale ◽  
Lucia Velluto ◽  
Marta Di Nicola ◽  
Chiara D’Angelo ◽  
Erica Costantini ◽  
...  

The role of inflammation and dysfunction of the cholinergic system in obstructive sleep apnea (OSA) has not exhaustively clarified. Thus, in this study, we explore the non-neuronal cholinergic system and the balance of T helper (Th) 17- and T regulatory (Treg)-related cytokines in OSA patients. The study includes 33 subjects with obstructive sleep apnea and 10 healthy controls (HC). The expression levels of cholinergic system component, RAR-related orphan receptor (RORc), transcription factor forkhead box protein 3 (Foxp3) and cytokines were evaluated. Th17- and Treg-related cytokines, choline levels and acetylcholinesterase (AChE), butyrylcholinesterase (BuChE) activity were quantified in OSA and control subjects. AChE and nicotinic receptor α 7 subunit (α7nAChR) gene expression and serum levels of choline, AChE and BuChE were lower in OSA patients than in the HC group. Compared with the HC group, OSA patients exhibited an increased expression, secretion and serum levels of pro-inflammatory cytokines, a reduced expression, secretion and serum levels of transforming growth factor (TGF)β and reduced Foxp3 mRNA levels. The Th17/Treg-related cytokine ratio was higher in the OSA group. Our results confirm and reinforce the hypothesis that OSA may be considered a systemic inflammatory disease, and that an imbalance of non-neuronal cholinergic and pro/anti-inflammatory cytokines may contribute to development and progression of comorbidities in OSA subjects. The evaluation of Th17/Treg-related cytokine may provide an additional explanation for OSA pathogenesis and clinical features, opening new directions for the OSA management.


Medicine ◽  
2016 ◽  
Vol 95 (41) ◽  
pp. e4944 ◽  
Author(s):  
Yu-Shu Huang ◽  
Christian Guilleminault ◽  
Fang-Ming Hwang ◽  
Chuan Cheng ◽  
Cheng-Hui Lin ◽  
...  

2010 ◽  
Vol 130 (12) ◽  
pp. 1394-1398 ◽  
Author(s):  
Young Gyu Eun ◽  
Myung Gu Kim ◽  
Kee Hwan Kwon ◽  
Seung Youp Shin ◽  
Joong Saeng Cho ◽  
...  

2016 ◽  
Vol 64 (4) ◽  
pp. 968.2-969
Author(s):  
G Salem ◽  
R Jambeih ◽  
H Hussein ◽  
H Bhardwaj J Keddissi ◽  
H Youness

IntroductionLung cancer accounts for 30% of all cancer deaths in the United States each year. Chronic inflammation has been linked to various steps involved in tumorigenesis. Several pro-inflammatory gene products have been identified that mediate a critical role in suppression of apoptosis, proliferation, angiogenesis, invasion, and metastasis. Among these gene products are Tumor Necrosis Factor (TNF), Interleukin (IL)-1a, IL-1b, IL-6, IL-8, and IL-18. The expression of all these genes is mainly regulated by the transcription factor nuclear factor kappa B (NF-kB), which is constitutively active in most tumors. Apnea-induced hypoxia and reoxygenation generates reactive oxygen species, which activate NF-kB and increase the systemic inflammation. Significant higher levels of pro-inflammatory cytokines TNF-α and IL-6, as well as a decrease in anti-inflammatory cytokines such as IL-10 has been found in obstructive sleep apnea (OSA). Previous studies showed that overnight oxygen desaturation seen in patients with OSA is associated with increased cancer incidence and cancer related mortality; The purpose of this study was to determine if OSA is an independent risk for the development and dissemination of malignancy, including lung cancer.MethodsThis is a retrospective case control chart review study conducted at the Oklahoma City Veterans Affairs Medical Center (VAMC). All adult patients who had a sleep study done between January 1st, 2000 and December 31st, 2007 were included. Patients were divided into 2 groups, based on whether they have OSA or not. The primary outcome was the rate of lung cancer occurring between 1998 and 2012. The secondary outcome was the rate of all cancers occurring during the same period. Fisher exact test was used to compare these rates.ResultsNine hundred two patients with a sleep study done between 2000 and 2007 were reviewed. Fifty seven patients were excluded since complete sleep study data were not available. Seven hundred and seventy five patients had sleep apnea (91.7%). Lung cancer occurred in 26/775 (3.4%) patients with OSA, vs. 3/70 (4.3%) patients without OSA (p=0.7). The rate of all malignancies was 19% (148/775) in patients with OSA compared to 15.7% (11/70) in patients without OSA (p=0.6).ConclusionSleep apnea does not appear to increase the risk of malignancy in general, and that of lung cancer in particular. Further studies to account for confounding risk factors are needed to definitively answer this question.


2021 ◽  
Vol 10 (2) ◽  
pp. 277 ◽  
Author(s):  
Antonino Maniaci ◽  
Giannicola Iannella ◽  
Salvatore Cocuzza ◽  
Claudio Vicini ◽  
Giuseppe Magliulo ◽  
...  

Obstructive Sleep Apnea Syndrome (OSAS) is a respiratory sleep disorder characterised by repeated episodes of partial or complete obstruction of the upper airway during the night. This obstruction usually occurs with a reduction (hypopnea) or complete cessation (apnea) of the airflow in the upper airways with the persistence of thoracic-diaphragmatic respiratory movements. During the hypopnea/apnea events, poor alveolar ventilation reduces the oxygen saturation in the arterial blood (SaO2) and a gradual increase in the partial arterial pressure of carbon dioxide (PaCO2). The direct consequence of the intermittent hypoxia is an oxidative imbalance, with reactive oxygen species production and the inflammatory cascade’s activation with pro and anti-inflammatory cytokines growth. Tumour necrosis factors, inflammatory cytokines (IL2, IL4, IL6), lipid peroxidation, and cell-free DNA have been found to increase in OSAS patients. However, even though different risk-related markers have been described and analysed in the literature, it has not yet been clarified whether specified inflammatory bio-markers better correlates with OSAS diagnosis and its clinical evolution/comorbidities. We perform a scientific literature review to discuss inflammatory and oxidative stress biomarkers currently tested in OSAS patients and their correlation with the disease’s severity and treatment.


2015 ◽  
Vol 16 ◽  
pp. S216-S217
Author(s):  
C. Cheng ◽  
Y. Huang ◽  
C. Guilleminault

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