OSA Is Associated With the Human Gut Microbiota Composition and Functional Potential in the Population-Based Swedish CardioPulmonary bioImage Study

被引:9
|
作者
Baldanzi, Gabriel [1 ]
Sayols-Baixeras, Sergi [1 ,2 ]
Theorell-Haglow, Jenny [1 ,3 ]
Dekkers, Koen F. [1 ]
Hammar, Ulf [1 ]
Nguyen, Diem [1 ]
Lin, Yi-Ting [1 ,4 ,5 ]
Ahmad, Shafqat [1 ,6 ]
Holm, Jacob Bak [7 ]
Nielsen, Henrik Bjorn [7 ]
Brunkwall, Louise [8 ]
Benedict, Christian [9 ]
Cedernaes, Jonathan [10 ,19 ]
Koskiniemi, Sanna [11 ]
Phillipson, Mia [10 ]
Lind, Lars [12 ]
Sundstrom, Johan [12 ,13 ]
Bergstrom, Goran [14 ,15 ]
Engstrom, Gunnar [8 ]
Smith, J. Gustav [16 ,17 ,18 ,20 ,21 ]
Orho-Melander, Marju [8 ]
Arnlov, Johan [4 ]
Kennedy, Beatrice [1 ]
Lindberg, Eva
Fall, Tove [1 ]
机构
[1] Uppsala Univ, Dept Med Sci, Mol Epidemiol & Sci Life Lab, Uppsala, Sweden
[2] Inst Salud Carlos III, CIBER Cardiovasc Dis CIBERCV, Madrid, Spain
[3] Uppsala Univ, Dept Med Sci Resp Allergy & Sleep Res, Uppsala, Sweden
[4] Karolinska Inst, Div Family Med & Primary Care, Dept Neurobiol Care Sci & Soc, Huddinge, Sweden
[5] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Dept Family Med, Kaohsiung, Taiwan
[6] Brigham & Womens Hosp, Harvard Med Sch, Prevent Med Div, Boston, MA USA
[7] Clin Microbi AS, Copenhagen, Denmark
[8] Lund Univ, Lund Univ Diabet Ctr, Dept Clin Sci Malmo, SE-20502 Malmo, Sweden
[9] Uppsala Univ, Dept Pharmaceut Biosci, Mol Neuropharmacol Sleep Sci Lab, Uppsala, Sweden
[10] Uppsala Univ, Dept Med Cell Biol, Sci Life Lab, Uppsala, Sweden
[11] Uppsala Univ, Dept Cell & Mol Biol, Uppsala, Sweden
[12] Uppsala Univ, Dept Med Sci Clin Epidemiol, Uppsala, Sweden
[13] Univ New South Wales, George Inst Global Hlth, Sydney, NSW, Australia
[14] Univ Gothenburg, Dept Mol & Clin Med, Sahlgrenska Acad, Inst Med, Gothenburg, Sweden
[15] Sahlgrens Univ Hosp, Dept Clin Physiol, Reg Vastra Gotaland, Gothenburg, Sweden
[16] Gothenburg Univ, Inst Med, Dept Mol & Clin Med, Wallenberg Lab, Gothenburg, Sweden
[17] Lund Univ, Dept Cardiol, Clin Sci, Lund, Sweden
[18] Skane Univ Hosp, Lund, Sweden
[19] Uppsala Univ, Dept Med Sci, Sci Life Lab, Uppsala, Sweden
[20] Lund Univ, Wallenberg Ctr Mol Med, Lund, Sweden
[21] Lund Univ, Diabet Ctr, Lund, Sweden
基金
欧洲研究理事会; 瑞典研究理事会;
关键词
epidemiology; microbiota; OSA; OBSTRUCTIVE SLEEP-APNEA; PREVALENCE; DIVERSITY; FEATURES; OBESITY;
D O I
10.1016/j.chest.2023.03.010
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
BACKGROUND: OSA is a common sleep-breathing disorder linked to increased risk of cardiovascular disease. Intermittent upper airway obstruction and hypoxia, hallmarks of OSA, have been shown in animal models to induce substantial changes to the gut microbiota composition, and subsequent transplantation of fecal matter to other animals induced changes in BP and glucose metabolism. RESEARCH QUESTION: Does OSA in adults associate with the composition and functional potential of the human gut microbiota? STUDY DESIGN AND METHODS: We used respiratory polygraphy data from up to 3,570 individuals 50 to 64 years of age from the population-based Swedish Cardiopulmonary bioimage Study combined with deep shotgun metagenomics of fecal samples to identify crosssectional associations between three OSA parameters covering apneas and hypopneas, cumulative sleep time in hypoxia, and number of oxygen desaturation events with gut microbiota composition. Data collection about potential confounders was based on questionnaires, onsite anthropometric measurements, plasma metabolomics, and linkage with the Swedish Prescribed Drug Register. RESULTS: We found that all three OSA parameters were associated with lower diversity of species in the gut. Furthermore, in multivariable-adjusted analysis, the OSA-related hypoxia parameters were associated with the relative abundance of 128 gut bacterial species, including higher abundance of Blautia obeum and Collinsella aerofaciens. The latter species was also independently associated with increased systolic BP. Furthermore, the cumulative time in hypoxia during sleep was associated with the abundance of genes involved in nine gut microbiota metabolic pathways, including propionate production from lactate. Finally, we observed two heterogeneous sets of plasma metabolites with opposite association with species positively and negatively associated with hypoxia parameters, respectively. INTERPRETATION: OSA-related hypoxia, but not the number of apneas/hypopneas, is associated with specific gut microbiota species and functions. Our findings lay the foundation for future research on the gut microbiota-mediated health effects of OSA.
引用
收藏
页码:503 / 516
页数:14
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