A Novel Role of Growth Differentiation Factor (GDF)-15 in Overlap with Sedentary Lifestyle and Cognitive Risk in COPD
Sedentary behavior and cognitive impairment have a direct impact on patients’ outcomes. An energy metabolic disorder may be involved in the overlap of these comorbid conditions (motoric cognitive risk (MCR)) in patients with chronic obstructive pulmonary disease (COPD). We aimed to explore the linka...
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Published in | Journal of clinical medicine Vol. 9; no. 9; p. 2737 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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24.08.2020
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ISSN | 2077-0383 2077-0383 |
DOI | 10.3390/jcm9092737 |
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Abstract | Sedentary behavior and cognitive impairment have a direct impact on patients’ outcomes. An energy metabolic disorder may be involved in the overlap of these comorbid conditions (motoric cognitive risk (MCR)) in patients with chronic obstructive pulmonary disease (COPD). We aimed to explore the linkage between a proapoptotic protein, growth differentiation factor (GDF)-15, and MCR. Physical activity (PA), cognitive function (Japanese version of the Montreal Cognitive Assessment: MOCA-J), and the serum GDF-15 levels were assessed in healthy subjects (n = 14), asthmatics (n = 22), and COPD patients (n = 28). In the entire cohort, serum GDF-15 had negative correlations with exercise (Ex) (ρ = −0.43, p < 0.001) and MoCA-J (ρ = −0.44, p < 0.001), and Ex and MOCA-J showed a positive correlation (ρ = 0.52, p < 0.0001). Compared to healthy subjects and asthmatics, COPD patients showed the highest serum GDF-15 levels and had a significantly higher proportion of subjects with MCR (both sedentary lifestyle (EX < 1.5) and cognitive risk (MoCA-J ≤ 25)). Also, we found that serum GDF-15 has a screening potential (100% sensitivity) greater than aging (67% sensitivity) for detecting MCR in COPD patients. In conclusion, higher serum GDF-15 had interrelationships with a sedentary lifestyle and cognitive risk. This protein was not disease-specific but could be a screening biomarker to detect MCR related to poor health outcomes of COPD patients. |
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AbstractList | Sedentary behavior and cognitive impairment have a direct impact on patients’ outcomes. An energy metabolic disorder may be involved in the overlap of these comorbid conditions (motoric cognitive risk (MCR)) in patients with chronic obstructive pulmonary disease (COPD). We aimed to explore the linkage between a proapoptotic protein, growth differentiation factor (GDF)-15, and MCR. Physical activity (PA), cognitive function (Japanese version of the Montreal Cognitive Assessment: MOCA-J), and the serum GDF-15 levels were assessed in healthy subjects (
n
= 14), asthmatics (
n
= 22), and COPD patients (
n
= 28). In the entire cohort, serum GDF-15 had negative correlations with exercise (Ex) (
ρ
= −0.43,
p
< 0.001) and MoCA-J (
ρ
= −0.44,
p
< 0.001), and Ex and MOCA-J showed a positive correlation (
ρ
= 0.52,
p
< 0.0001). Compared to healthy subjects and asthmatics, COPD patients showed the highest serum GDF-15 levels and had a significantly higher proportion of subjects with MCR (both sedentary lifestyle (EX < 1.5) and cognitive risk (MoCA-J ≤ 25)). Also, we found that serum GDF-15 has a screening potential (100% sensitivity) greater than aging (67% sensitivity) for detecting MCR in COPD patients. In conclusion, higher serum GDF-15 had interrelationships with a sedentary lifestyle and cognitive risk. This protein was not disease-specific but could be a screening biomarker to detect MCR related to poor health outcomes of COPD patients. Sedentary behavior and cognitive impairment have a direct impact on patients’ outcomes. An energy metabolic disorder may be involved in the overlap of these comorbid conditions (motoric cognitive risk (MCR)) in patients with chronic obstructive pulmonary disease (COPD). We aimed to explore the linkage between a proapoptotic protein, growth differentiation factor (GDF)-15, and MCR. Physical activity (PA), cognitive function (Japanese version of the Montreal Cognitive Assessment: MOCA-J), and the serum GDF-15 levels were assessed in healthy subjects (n = 14), asthmatics (n = 22), and COPD patients (n = 28). In the entire cohort, serum GDF-15 had negative correlations with exercise (Ex) (ρ = −0.43, p < 0.001) and MoCA-J (ρ = −0.44, p < 0.001), and Ex and MOCA-J showed a positive correlation (ρ = 0.52, p < 0.0001). Compared to healthy subjects and asthmatics, COPD patients showed the highest serum GDF-15 levels and had a significantly higher proportion of subjects with MCR (both sedentary lifestyle (EX < 1.5) and cognitive risk (MoCA-J ≤ 25)). Also, we found that serum GDF-15 has a screening potential (100% sensitivity) greater than aging (67% sensitivity) for detecting MCR in COPD patients. In conclusion, higher serum GDF-15 had interrelationships with a sedentary lifestyle and cognitive risk. This protein was not disease-specific but could be a screening biomarker to detect MCR related to poor health outcomes of COPD patients. Sedentary behavior and cognitive impairment have a direct impact on patients' outcomes. An energy metabolic disorder may be involved in the overlap of these comorbid conditions (motoric cognitive risk (MCR)) in patients with chronic obstructive pulmonary disease (COPD). We aimed to explore the linkage between a proapoptotic protein, growth differentiation factor (GDF)-15, and MCR. Physical activity (PA), cognitive function (Japanese version of the Montreal Cognitive Assessment: MOCA-J), and the serum GDF-15 levels were assessed in healthy subjects ( = 14), asthmatics ( = 22), and COPD patients ( = 28). In the entire cohort, serum GDF-15 had negative correlations with exercise (Ex) ( = -0.43, < 0.001) and MoCA-J ( = -0.44, < 0.001), and Ex and MOCA-J showed a positive correlation ( = 0.52, < 0.0001). Compared to healthy subjects and asthmatics, COPD patients showed the highest serum GDF-15 levels and had a significantly higher proportion of subjects with MCR (both sedentary lifestyle (EX < 1.5) and cognitive risk (MoCA-J ≤ 25)). Also, we found that serum GDF-15 has a screening potential (100% sensitivity) greater than aging (67% sensitivity) for detecting MCR in COPD patients. In conclusion, higher serum GDF-15 had interrelationships with a sedentary lifestyle and cognitive risk. This protein was not disease-specific but could be a screening biomarker to detect MCR related to poor health outcomes of COPD patients. Sedentary behavior and cognitive impairment have a direct impact on patients' outcomes. An energy metabolic disorder may be involved in the overlap of these comorbid conditions (motoric cognitive risk (MCR)) in patients with chronic obstructive pulmonary disease (COPD). We aimed to explore the linkage between a proapoptotic protein, growth differentiation factor (GDF)-15, and MCR. Physical activity (PA), cognitive function (Japanese version of the Montreal Cognitive Assessment: MOCA-J), and the serum GDF-15 levels were assessed in healthy subjects (n = 14), asthmatics (n = 22), and COPD patients (n = 28). In the entire cohort, serum GDF-15 had negative correlations with exercise (Ex) (ρ = -0.43, p < 0.001) and MoCA-J (ρ = -0.44, p < 0.001), and Ex and MOCA-J showed a positive correlation (ρ = 0.52, p < 0.0001). Compared to healthy subjects and asthmatics, COPD patients showed the highest serum GDF-15 levels and had a significantly higher proportion of subjects with MCR (both sedentary lifestyle (EX < 1.5) and cognitive risk (MoCA-J ≤ 25)). Also, we found that serum GDF-15 has a screening potential (100% sensitivity) greater than aging (67% sensitivity) for detecting MCR in COPD patients. In conclusion, higher serum GDF-15 had interrelationships with a sedentary lifestyle and cognitive risk. This protein was not disease-specific but could be a screening biomarker to detect MCR related to poor health outcomes of COPD patients.Sedentary behavior and cognitive impairment have a direct impact on patients' outcomes. An energy metabolic disorder may be involved in the overlap of these comorbid conditions (motoric cognitive risk (MCR)) in patients with chronic obstructive pulmonary disease (COPD). We aimed to explore the linkage between a proapoptotic protein, growth differentiation factor (GDF)-15, and MCR. Physical activity (PA), cognitive function (Japanese version of the Montreal Cognitive Assessment: MOCA-J), and the serum GDF-15 levels were assessed in healthy subjects (n = 14), asthmatics (n = 22), and COPD patients (n = 28). In the entire cohort, serum GDF-15 had negative correlations with exercise (Ex) (ρ = -0.43, p < 0.001) and MoCA-J (ρ = -0.44, p < 0.001), and Ex and MOCA-J showed a positive correlation (ρ = 0.52, p < 0.0001). Compared to healthy subjects and asthmatics, COPD patients showed the highest serum GDF-15 levels and had a significantly higher proportion of subjects with MCR (both sedentary lifestyle (EX < 1.5) and cognitive risk (MoCA-J ≤ 25)). Also, we found that serum GDF-15 has a screening potential (100% sensitivity) greater than aging (67% sensitivity) for detecting MCR in COPD patients. In conclusion, higher serum GDF-15 had interrelationships with a sedentary lifestyle and cognitive risk. This protein was not disease-specific but could be a screening biomarker to detect MCR related to poor health outcomes of COPD patients. |
Author | Ohata, Shuichiro Kakugawa, Tomoyuki Suga, Kazuyoshi Oishi, Keiji Ohteru, Yuichi Matsunaga, Kazuto Doi, Keiko Takahashi, Shun Chikumoto, Ayumi Harada, Misa Yamaji, Yoshikazu Edakuni, Nobutaka Hirano, Tsunahiko Asami-Noyama, Maki Murata, Yoriyuki Yasuda, Kasumi Suizu, Sumiteru Hamada, Kazuki Matsuda, Kazuki Uehara, Sho Donishi, Tomohiro Mimura, Yusuke Murakawa, Keita |
AuthorAffiliation | 3 Department of System Neurophysiology, Graduate School of Wakayama Medical University, Wakayama 641-8510, Japan; tdonishi@wakayama-med.ac.jp 7 Department of Pulmonology and Gerontology Graduate School of Medicine, Yamaguchi University, Ube 755-8505, Japan; tomoyukikakugawa@gmail.com 1 Department of Respiratory Medicine and Infectious Disease, Graduate School of Medicine, Yamaguchi University, Ube 755-8505, Japan; decem119@yamaguchi-u.ac.jp (K.D.); kazmatsu@yamaguchi-u.ac.jp (K.M.); hara-da@yamaguchi-u.ac.jp (M.H.); relativity.theory135@gmail.com (S.S.); murakawakeita124@gmail.com (K.M.); chiku05@yamaguchi-u.ac.jp (A.C.); yohteru@yamaguchi-u.ac.jp (Y.O.); k0m1a2t8s1u1d2a1@gmail.com (K.M.); n010eb.mie@gmail.com (S.U.); khamada@yamaguchi-u.ac.jp (K.H.); j015ebponyou@gmail.com (S.O.); yyamaji@yamaguchi-u.ac.jp (Y.Y.); noyamama@yamaguchi-u.ac.jp (M.A.-N.); edakuni@yamaguchi-u.ac.jp (N.E.) 2 Department of Neuropsychiatry, Wakayama Medical University, Wakayama 641-8510, Japan; t-shun@wakayama-m |
AuthorAffiliation_xml | – name: 7 Department of Pulmonology and Gerontology Graduate School of Medicine, Yamaguchi University, Ube 755-8505, Japan; tomoyukikakugawa@gmail.com – name: 5 Department of Medicine and Clinical Science, Graduate School of Medicine, Yamaguchi University, Ube 755-8505, Japan; ohishk@yamaguchi-u.ac.jp (K.O.); ymurata-ygc@umin.ac.jp (Y.M.) – name: 1 Department of Respiratory Medicine and Infectious Disease, Graduate School of Medicine, Yamaguchi University, Ube 755-8505, Japan; decem119@yamaguchi-u.ac.jp (K.D.); kazmatsu@yamaguchi-u.ac.jp (K.M.); hara-da@yamaguchi-u.ac.jp (M.H.); relativity.theory135@gmail.com (S.S.); murakawakeita124@gmail.com (K.M.); chiku05@yamaguchi-u.ac.jp (A.C.); yohteru@yamaguchi-u.ac.jp (Y.O.); k0m1a2t8s1u1d2a1@gmail.com (K.M.); n010eb.mie@gmail.com (S.U.); khamada@yamaguchi-u.ac.jp (K.H.); j015ebponyou@gmail.com (S.O.); yyamaji@yamaguchi-u.ac.jp (Y.Y.); noyamama@yamaguchi-u.ac.jp (M.A.-N.); edakuni@yamaguchi-u.ac.jp (N.E.) – name: 2 Department of Neuropsychiatry, Wakayama Medical University, Wakayama 641-8510, Japan; t-shun@wakayama-med.ac.jp (S.T.); y-kasumi@wakayama-med.ac.jp (K.Y.) – name: 3 Department of System Neurophysiology, Graduate School of Wakayama Medical University, Wakayama 641-8510, Japan; tdonishi@wakayama-med.ac.jp – name: 6 Department of Clinical Research, National Hospital Organization Yamaguchi Ube Medical Center, Ube 755-0241, Japan; mimuray-yumc@umin.ac.jp – name: 4 Department of Radiology, Semui PET Screening and Radiatiotherapeutic Site, St. Hill Hospital, Ube 755-0155, Japan; sugar@sthill-hp.or.jp |
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Keywords | comorbidity motoric cognitive risk cognitive impairment aging GDF-15 sedentary COPD |
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SubjectTerms | Age Aging Asthma Biomarkers Chronic illnesses Chronic obstructive pulmonary disease Clinical medicine Cognitive ability Comorbidity Inflammation Lifestyles Lung diseases Metabolic disorders Musculoskeletal system Proteins Sedentary behavior Trends |
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Title | A Novel Role of Growth Differentiation Factor (GDF)-15 in Overlap with Sedentary Lifestyle and Cognitive Risk in COPD |
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