PM20D1 is a circulating biomarker closely associated with obesity, insulin resistance and metabolic syndrome
Objective Peptidase M20 domain containing 1 (PM20D1), a secreted enzyme catalysing condensation of fatty acids and amino acids into the bioactive lipids N-acyl amino acids (NAAA), induces uncoupling protein 1 (UCP1)-independent adaptive thermogenesis in brown/beige adipocytes in mice. This study aim...
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Published in: | European journal of endocrinology Vol. 186; no. 2; pp. 151 - 161 |
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Main Authors: | , , , , , , , , , , , |
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Bioscientifica Ltd
01-02-2022
Oxford University Press |
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Abstract | Objective Peptidase M20 domain containing 1 (PM20D1), a secreted enzyme catalysing condensation of fatty acids and amino acids into the bioactive lipids N-acyl amino acids (NAAA), induces uncoupling protein 1 (UCP1)-independent adaptive thermogenesis in brown/beige adipocytes in mice. This study aimed to explore the associations of the circulating levels of PM20D1 and major NAAA with obesity-related metabolic complications in humans. Design and methods Serum concentrations of PM20D1 and NAAA (C18:1-Leu and C18:1-Phe) in 256 Chinese subjects, including 78 lean and 178 overweight/obese individuals with or without diabetes, were measured with immunoassays and liquid chromatography–mass spectrometry, respectively. The impact of sulfonylurea and rosiglitazone on their circulating levels was examined in 62 patients with type 2 diabetes. Results Serum PM20D1 level was significantly elevated in overweight/obese individuals and was closely associated with circulating levels of C18:1-Leu and C18:1-Phe. Furthermore, serum PM20D1, C18:1-Leu and C18:1-Phe concentrations correlated positively with several parameters of adiposity as well as fasting and 2 h postprandial glucose, HbA1c, fasting insulin and HOMA-IR independent of BMI and age. Moreover, a significant elevation in PM20D1, C18:1-Leu and C18:1-Phe concentrations corresponding with increases in the number of components of the metabolic syndrome (MetS) was observed. Treatment with sulfonylurea significantly decreased circulating PM20D1, C18:1-Leu and C18:1-Phe in patients with type 2 diabetes. Conclusions Increased serum levels of PM20D1 and its catalytic products NAAA are closely associated with obesity-related glucose dysregulation, insulin resistance and MetS and can be potentially used as clinical biomarkers for diagnosing and monitoring these disorders. |
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AbstractList | Objective Peptidase M20 domain containing 1 (PM20D1), a secreted enzyme catalysing condensation of fatty acids and amino acids into the bioactive lipids N-acyl amino acids (NAAA), induces uncoupling protein 1 (UCP1)-independent adaptive thermogenesis in brown/beige adipocytes in mice. This study aimed to explore the associations of the circulating levels of PM20D1 and major NAAA with obesity-related metabolic complications in humans. Design and methods Serum concentrations of PM20D1 and NAAA (C18:1-Leu and C18:1-Phe) in 256 Chinese subjects, including 78 lean and 178 overweight/obese individuals with or without diabetes, were measured with immunoassays and liquid chromatography–mass spectrometry, respectively. The impact of sulfonylurea and rosiglitazone on their circulating levels was examined in 62 patients with type 2 diabetes. Results Serum PM20D1 level was significantly elevated in overweight/obese individuals and was closely associated with circulating levels of C18:1-Leu and C18:1-Phe. Furthermore, serum PM20D1, C18:1-Leu and C18:1-Phe concentrations correlated positively with several parameters of adiposity as well as fasting and 2 h postprandial glucose, HbA1c, fasting insulin and HOMA-IR independent of BMI and age. Moreover, a significant elevation in PM20D1, C18:1-Leu and C18:1-Phe concentrations corresponding with increases in the number of components of the metabolic syndrome (MetS) was observed. Treatment with sulfonylurea significantly decreased circulating PM20D1, C18:1-Leu and C18:1-Phe in patients with type 2 diabetes. Conclusions Increased serum levels of PM20D1 and its catalytic products NAAA are closely associated with obesity-related glucose dysregulation, insulin resistance and MetS and can be potentially used as clinical biomarkers for diagnosing and monitoring these disorders. Peptidase M20 domain containing 1 (PM20D1), a secreted enzyme catalysing condensation of fatty acids and amino acids into the bioactive lipids N-acyl amino acids (NAAA), induces uncoupling protein 1 (UCP1)-independent adaptive thermogenesis in brown/beige adipocytes in mice. This study aimed to explore the associations of the circulating levels of PM20D1 and major NAAA with obesity-related metabolic complications in humans. Serum concentrations of PM20D1 and NAAA (C18:1-Leu and C18:1-Phe) in 256 Chinese subjects, including 78 lean and 178 overweight/obese individuals with or without diabetes, were measured with immunoassays and liquid chromatography-mass spectrometry, respectively. The impact of sulfonylurea and rosiglitazone on their circulating levels was examined in 62 patients with type 2 diabetes. Serum PM20D1 level was significantly elevated in overweight/obese individuals and was closely associated with circulating levels of C18:1-Leu and C18:1-Phe. Furthermore, serum PM20D1, C18:1-Leu and C18:1-Phe concentrations correlated positively with several parameters of adiposity as well as fasting and 2 h postprandial glucose, HbA1c, fasting insulin and HOMA-IR independent of BMI and age. Moreover, a significant elevation in PM20D1, C18:1-Leu and C18:1-Phe concentrations corresponding with increases in the number of components of the metabolic syndrome (MetS) was observed. Treatment with sulfonylurea significantly decreased circulating PM20D1, C18:1-Leu and C18:1-Phe in patients with type 2 diabetes. Increased serum levels of PM20D1 and its catalytic products NAAA are closely associated with obesity-related glucose dysregulation, insulin resistance and MetS and can be potentially used as clinical biomarkers for diagnosing and monitoring these disorders. OBJECTIVEPeptidase M20 domain containing 1 (PM20D1), a secreted enzyme catalysing condensation of fatty acids and amino acids into the bioactive lipids N-acyl amino acids (NAAA), induces uncoupling protein 1 (UCP1)-independent adaptive thermogenesis in brown/beige adipocytes in mice. This study aimed to explore the associations of the circulating levels of PM20D1 and major NAAA with obesity-related metabolic complications in humans. DESIGN AND METHODSSerum concentrations of PM20D1 and NAAA (C18:1-Leu and C18:1-Phe) in 256 Chinese subjects, including 78 lean and 178 overweight/obese individuals with or without diabetes, were measured with immunoassays and liquid chromatography-mass spectrometry, respectively. The impact of sulfonylurea and rosiglitazone on their circulating levels was examined in 62 patients with type 2 diabetes. RESULTSSerum PM20D1 level was significantly elevated in overweight/obese individuals and was closely associated with circulating levels of C18:1-Leu and C18:1-Phe. Furthermore, serum PM20D1, C18:1-Leu and C18:1-Phe concentrations correlated positively with several parameters of adiposity as well as fasting and 2 h postprandial glucose, HbA1c, fasting insulin and HOMA-IR independent of BMI and age. Moreover, a significant elevation in PM20D1, C18:1-Leu and C18:1-Phe concentrations corresponding with increases in the number of components of the metabolic syndrome (MetS) was observed. Treatment with sulfonylurea significantly decreased circulating PM20D1, C18:1-Leu and C18:1-Phe in patients with type 2 diabetes. CONCLUSIONSIncreased serum levels of PM20D1 and its catalytic products NAAA are closely associated with obesity-related glucose dysregulation, insulin resistance and MetS and can be potentially used as clinical biomarkers for diagnosing and monitoring these disorders. Objective Peptidase M20 domain containing 1 (PM20D1), a secreted enzyme catalysing condensation of fatty acids and amino acids into the bioactive lipids N-acyl amino acids (NAAA), induces uncoupling protein 1 (UCP1)-independent adaptive thermogenesis in brown/beige adipocytes in mice. This study aimed to explore the associations of the circulating levels of PM20D1 and major NAAA with obesity-related metabolic complications in humans. Design and methods Serum concentrations of PM20D1 and NAAA (C18:1-Leu and C18:1-Phe) in 256 Chinese subjects, including 78 lean and 178 overweight/obese individuals with or without diabetes, were measured with immunoassays and liquid chromatography–mass spectrometry, respectively. The impact of sulfonylurea and rosiglitazone on their circulating levels was examined in 62 patients with type 2 diabetes. Results Serum PM20D1 level was significantly elevated in overweight/obese individuals and was closely associated with circulating levels of C18:1-Leu and C18:1-Phe. Furthermore, serum PM20D1, C18:1-Leu and C18:1-Phe concentrations correlated positively with several parameters of adiposity as well as fasting and 2 h postprandial glucose, HbA1c, fasting insulin and HOMA-IR independent of BMI and age. Moreover, a significant elevation in PM20D1, C18:1-Leu and C18:1-Phe concentrations corresponding with increases in the number of components of the metabolic syndrome (MetS) was observed. Treatment with sulfonylurea significantly decreased circulating PM20D1, C18:1-Leu and C18:1-Phe in patients with type 2 diabetes. Conclusions Increased serum levels of PM20D1 and its catalytic products NAAA are closely associated with obesity-related glucose dysregulation, insulin resistance and MetS and can be potentially used as clinical biomarkers for diagnosing and monitoring these disorders. |
Author | Liu, Yan Lam, Karen S L Diaz-Canestro, Candela Cheng, Kenneth K Y Yang, Ranyao Song, Erfei Hu, Yue Lee, Chi Ho Fong, Carol Ho Yi Xu, Aimin Lin, Huige Pravelil, Aparna Padmanabhan |
AuthorAffiliation | Department of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China Department of Metabolic and Bariatric Surgery, The First Affiliated Hospital of Jinan University, Guangzhou, China Department of Medicine, The University of Hong Kong, Hong Kong, China Department of Pharmacology and Pharmacy, The University of Hong Kong, Hong Kong, China Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, China State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China |
AuthorAffiliation_xml | – name: State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China – name: Department of Medicine, The University of Hong Kong, Hong Kong, China – name: Department of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China – name: Department of Metabolic and Bariatric Surgery, The First Affiliated Hospital of Jinan University, Guangzhou, China – name: Department of Pharmacology and Pharmacy, The University of Hong Kong, Hong Kong, China – name: Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, China |
Author_xml | – sequence: 1 givenname: Ranyao surname: Yang fullname: Yang, Ranyao organization: Department of Medicine, The University of Hong Kong, Hong Kong, China – sequence: 2 givenname: Yue surname: Hu fullname: Hu, Yue organization: Department of Medicine, The University of Hong Kong, Hong Kong, China – sequence: 3 givenname: Chi Ho surname: Lee fullname: Lee, Chi Ho organization: Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, China – sequence: 4 givenname: Yan surname: Liu fullname: Liu, Yan organization: Department of Medicine, The University of Hong Kong, Hong Kong, China – sequence: 5 givenname: Candela surname: Diaz-Canestro fullname: Diaz-Canestro, Candela organization: Department of Medicine, The University of Hong Kong, Hong Kong, China – sequence: 6 givenname: Carol Ho Yi surname: Fong fullname: Fong, Carol Ho Yi organization: Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, China – sequence: 7 givenname: Huige surname: Lin fullname: Lin, Huige organization: Department of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China – sequence: 8 givenname: Kenneth K Y surname: Cheng fullname: Cheng, Kenneth K Y organization: Department of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China – sequence: 9 givenname: Aparna Padmanabhan surname: Pravelil fullname: Pravelil, Aparna Padmanabhan organization: Department of Medicine, The University of Hong Kong, Hong Kong, China – sequence: 10 givenname: Erfei surname: Song fullname: Song, Erfei organization: Department of Metabolic and Bariatric Surgery, The First Affiliated Hospital of Jinan University, Guangzhou, China – sequence: 11 givenname: Karen S L surname: Lam fullname: Lam, Karen S L email: ksllam@hku.hk, amxu@hku.hk organization: Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, China – sequence: 12 givenname: Aimin surname: Xu fullname: Xu, Aimin email: ksllam@hku.hk, amxu@hku.hk organization: Department of Pharmacology and Pharmacy, The University of Hong Kong, Hong Kong, China |
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Snippet | Objective Peptidase M20 domain containing 1 (PM20D1), a secreted enzyme catalysing condensation of fatty acids and amino acids into the bioactive lipids N-acyl... Peptidase M20 domain containing 1 (PM20D1), a secreted enzyme catalysing condensation of fatty acids and amino acids into the bioactive lipids N-acyl amino... Objective Peptidase M20 domain containing 1 (PM20D1), a secreted enzyme catalysing condensation of fatty acids and amino acids into the bioactive lipids N-acyl... OBJECTIVEPeptidase M20 domain containing 1 (PM20D1), a secreted enzyme catalysing condensation of fatty acids and amino acids into the bioactive lipids N-acyl... |
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SubjectTerms | Adipocytes Adipose tissue Adult Aged Amidohydrolases - blood Amino acids Biomarkers Biomarkers - blood Body weight Clinical Study Cross-Sectional Studies Diabetes Diabetes mellitus (non-insulin dependent) Fatty acids Female HEK293 Cells Humans Insulin Insulin resistance Insulin Resistance - physiology Lipids Liquid chromatography Male Mass spectroscopy Metabolic syndrome Metabolic Syndrome - blood Metabolic Syndrome - diagnosis Middle Aged Obesity Obesity - blood Obesity - diagnosis Overweight Patients Peptidase Rosiglitazone Serum levels Sulfonylurea Thermogenesis Uncoupling protein 1 |
Title | PM20D1 is a circulating biomarker closely associated with obesity, insulin resistance and metabolic syndrome |
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