TY - JOUR
T1 - Sleep disordered breathing and haemoglobin A1c levels within or over normal range and ageing or sex differences
T2 - the Nagahama study
AU - Matsumoto, Takeshi
AU - Murase, Kimihiko
AU - Tabara, Yasuharu
AU - Minami, Takuma
AU - Kanai, Osamu
AU - Takeyama, Hirofumi
AU - Sunadome, Hironobu
AU - Nagasaki, Tadao
AU - Takahashi, Naomi
AU - Nakatsuka, Yoshinari
AU - Hamada, Satoshi
AU - Handa, Tomohiro
AU - Tanizawa, Kiminobu
AU - Nakamoto, Isuzu
AU - Wakamura, Tomoko
AU - Komenami, Naoko
AU - Setoh, Kazuya
AU - Kawaguchi, Takahisa
AU - Tsutsumi, Takanobu
AU - Morita, Satoshi
AU - Takahashi, Yoshimitsu
AU - Nakayama, Takeo
AU - Sato, Susumu
AU - Hirai, Toyohiro
AU - Matsuda, Fumihiko
AU - Chin, Kazuo
N1 - Funding Information:
Japan Agency for Medical Research and Development; Ministry of Education, Culture, Sports, Science and Technology; Ministry of Health, Labor and Welfare; Ministry of Education, Culture, Sports, Science and Technology in Japan, Grant/Award Numbers: 18K18450, 17H04123, 17H04126, 17H04182, 26293198, 26670313, 25293141, 20H03690; the Center of Innovation Program; Global University Project from Japan Science and Technology Agency; Japan Agency for Medical Research and Development (AMED), Grant/Award Numbers: le0110005, wm0425018, ek0210116, ek0210096, ek0210066, kk0205008, ek0109348, ek0109196, ek0109283, ek0109070, ek0210150, dk0207027, dk0207006; the Intractable Respiratory Diseases; Pulmonary Hypertension Research Group from the Ministry of Health, Labour and Welfare of Japan; the Takeda Medical Research Foundation; Mitsubishi Foundation, Daiwa Securities Health Foundation; Sumitomo Foundation; Research Foundation for Healthy Aging; Health, Labour and Welfare Sciences Research Grants, Research on Region Medical; Philips Japan; ResMed Japan; Fukuda Denshi; Fukuda Lifetec Tokyo Funding information
Funding Information:
We are grateful to Nagahama City Office and the non-profit organisation Zeroji Club for their assistance in performing the Nagahama study. We are grateful to Yoshiro Toyama, Masanori Azuma, Ryo Tachikawa, and Morito Inouchi for their assistance in collecting data. We are also grateful to Shunsuke Nagashima, Chiaki Tojo and Makoto Yamashita for their assistance in analysing the actigraphy data.
Funding Information:
This study was funded by a University Grant, a Grant‐in‐Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology in Japan (20H03690, 25293141, 26670313, 26293198, 17H04182, 17H04126, 17H04123, 18K18450), the Center of Innovation Program, and the Global University Project from Japan Science and Technology Agency, Japan Agency for Medical Research and Development (AMED) under Grant Numbers dk0207006, dk0207027, ek0210150, ek0109070, ek0109283, ek0109196, ek0109348, kk0205008, ek0210066, ek0210096, ek0210116, wm0425018, and le0110005, grants from the Japanese Ministry of Education, Culture, Sports, Science and Technology, the Intractable Respiratory Diseases and Pulmonary Hypertension Research Group from the Ministry of Health, Labour and Welfare of Japan (H29‐intractable diseases‐general‐027, 20FC1027), the Takeda Medical Research Foundation, Mitsubishi Foundation, Daiwa Securities Health Foundation, Sumitomo Foundation, the Research Foundation for Healthy Aging, and Health, Labour and Welfare Sciences Research Grants, Research on Region Medical (H28‐iryo‐ippan‐016, H30‐iryo‐ippan‐009). This was not an industry‐supported study. Department of Sleep Medicine and Respiratory Care is funded by endowments from Philips Japan, ResMed Japan, Fukuda Denshi and Fukuda Lifetec Tokyo to Nihon University.
Publisher Copyright:
© 2022 European Sleep Research Society.
PY - 2022
Y1 - 2022
N2 - Recently an association between blood glucose dysregulation and sleep disruption was suggested. The association between sleep disordered breathing, most of which is due to obstructive sleep apnea (OSA) in the general population, and diabetic severity, as well as the impact of antidiabetic treatment, remains unclear. This study aimed to investigate these associations as well as age and sex differences. This cross-sectional study evaluated 7,680 community participants as the main cohort (population-based cohort). OSA was assessed by the 3% oxygen desaturation index from pulse oximetry, which was corrected for sleep duration obtained by wrist actigraphy. For arguing the limitations for using pulse oximetry, 597 hospitalised patients, who were assessed by the apnea–hypopnea index from attended polysomnography, were also evaluated as the validation cohort (hospital-based cohort). Moderate-to-severe OSA was more prevalent as haemoglobin A1c (HbA1c) levels increased (<5.6%/5.6%–<6.5%/6.5%–<7.5%/≥7.5%, respectively) in both cohorts (p < 0.001), but only in those without antidiabetic treatment. The HbA1c level was an independent factor for moderate-to-severe OSA (population-based cohort, odds ratio [OR] 1.26, 95% confidence interval [CI] 1.10–1.45; hospital-based cohort, OR 1.69, 95% CI 1.22–2.33, per 1% increase). These associations were more prominent in the middle-aged (aged <60 years) than in the elderly (aged ≥60 years) and in women than in men in both cohorts. The prevalence of moderate-to-severe OSA in patients with antidiabetic treatment in the hospital-based cohort was ≥75% regardless of HbA1c levels. In conclusion, an association between the prevalence of OSA and HbA1c level even within or over the normal range was found only in patients without antidiabetic treatment and was more prominent in the middle-aged and in women.
AB - Recently an association between blood glucose dysregulation and sleep disruption was suggested. The association between sleep disordered breathing, most of which is due to obstructive sleep apnea (OSA) in the general population, and diabetic severity, as well as the impact of antidiabetic treatment, remains unclear. This study aimed to investigate these associations as well as age and sex differences. This cross-sectional study evaluated 7,680 community participants as the main cohort (population-based cohort). OSA was assessed by the 3% oxygen desaturation index from pulse oximetry, which was corrected for sleep duration obtained by wrist actigraphy. For arguing the limitations for using pulse oximetry, 597 hospitalised patients, who were assessed by the apnea–hypopnea index from attended polysomnography, were also evaluated as the validation cohort (hospital-based cohort). Moderate-to-severe OSA was more prevalent as haemoglobin A1c (HbA1c) levels increased (<5.6%/5.6%–<6.5%/6.5%–<7.5%/≥7.5%, respectively) in both cohorts (p < 0.001), but only in those without antidiabetic treatment. The HbA1c level was an independent factor for moderate-to-severe OSA (population-based cohort, odds ratio [OR] 1.26, 95% confidence interval [CI] 1.10–1.45; hospital-based cohort, OR 1.69, 95% CI 1.22–2.33, per 1% increase). These associations were more prominent in the middle-aged (aged <60 years) than in the elderly (aged ≥60 years) and in women than in men in both cohorts. The prevalence of moderate-to-severe OSA in patients with antidiabetic treatment in the hospital-based cohort was ≥75% regardless of HbA1c levels. In conclusion, an association between the prevalence of OSA and HbA1c level even within or over the normal range was found only in patients without antidiabetic treatment and was more prominent in the middle-aged and in women.
KW - elderly
KW - general population
KW - menopause
KW - obstructive sleep apnea
KW - type 2 diabetes
UR - http://www.scopus.com/inward/record.url?scp=85142875270&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85142875270&partnerID=8YFLogxK
U2 - 10.1111/jsr.13795
DO - 10.1111/jsr.13795
M3 - Article
AN - SCOPUS:85142875270
SN - 0962-1105
VL - 32
JO - Journal of Sleep Research
JF - Journal of Sleep Research
IS - 3
M1 - e13795
ER -