Hepatokine leukocyte cell‐derived chemotaxin 2 as a biomarker of insulin resistance, liver enzymes, and metabolic dysfunction‐associated steatotic liver disease in the general population

ABSTRACT Aims/Introduction Leukocyte cell‐derived chemotaxin 2 (LECT2) is an obesity‐associated hepatokine that causes skeletal muscle insulin resistance. Since LECT2 is up‐regulated by the inactivation of the energy sensor AMPK in the liver, we hypothesized that LECT2 has potential as a biomarker f...

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Main Authors: Keita Suzuki, Hiromasa Tsujiguchi, Akinori Hara, Yumie Takeshita, Hisanori Goto, Yujiro Nakano, Reina Yamamoto, Hiroaki Takayama, Atsushi Tajima, Tatsuya Yamashita, Masao Honda, Hiroyuki Nakamura, Toshinari Takamura
Format: Article
Language:English
Published: Wiley 2025-02-01
Series:Journal of Diabetes Investigation
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Online Access:https://doi.org/10.1111/jdi.14351
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author Keita Suzuki
Hiromasa Tsujiguchi
Akinori Hara
Yumie Takeshita
Hisanori Goto
Yujiro Nakano
Reina Yamamoto
Hiroaki Takayama
Atsushi Tajima
Tatsuya Yamashita
Masao Honda
Hiroyuki Nakamura
Toshinari Takamura
author_facet Keita Suzuki
Hiromasa Tsujiguchi
Akinori Hara
Yumie Takeshita
Hisanori Goto
Yujiro Nakano
Reina Yamamoto
Hiroaki Takayama
Atsushi Tajima
Tatsuya Yamashita
Masao Honda
Hiroyuki Nakamura
Toshinari Takamura
author_sort Keita Suzuki
collection DOAJ
description ABSTRACT Aims/Introduction Leukocyte cell‐derived chemotaxin 2 (LECT2) is an obesity‐associated hepatokine that causes skeletal muscle insulin resistance. Since LECT2 is up‐regulated by the inactivation of the energy sensor AMPK in the liver, we hypothesized that LECT2 has potential as a biomarker for metabolic dysfunction‐associated steatotic liver disease (MASLD). Therefore, we investigated whether circulating LECT2 levels are associated with insulin sensitivity, liver enzymes, and MASLD. Materials and Methods This cross‐sectional study included 138 Japanese individuals. Plasma LECT2 levels were measured using fasting blood samples. B‐mode ultrasonography was used to assess hepatic steatosis. Results The mean age and body mass index (BMI) of participants were 63.5 ± 10.2 years and 23.0 ± 3.1 kg/m2, respectively. Higher LECT2 levels positively correlated with homeostatic model assessment for insulin resistance (HOMA‐IR) values and negatively correlated with the quantitative insulin sensitivity check index (QUICKI) among all participants (HOMA‐IR; non‐standardized β (B) = 6.38, P < 0.01: QUICKI; B = −161, P < 0.01). These correlations were stronger in the low BMI group (HOMA‐IR; B = 13.85, P < 0.01: QUICKI; B = −180, P < 0.01). LECT2 levels also positively correlated with gamma‐glutamyl transferase levels (B = 0.01, P = 0.01) and alanine aminotransferase levels (B = 0.33, P = 0.02). Higher LECT2 levels correlated with the prevalence of MASLD (odds ratio = 1.14, P = 0.02). Conclusions The present results suggest the potential of plasma LECT2 levels as a biomarker for insulin resistance in individuals who are not overweight and the prevalence of MASLD in the general population.
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spelling doaj-art-27f6288c3c2e409fafc912f719179bf22025-02-01T10:02:01ZengWileyJournal of Diabetes Investigation2040-11162040-11242025-02-0116229830810.1111/jdi.14351Hepatokine leukocyte cell‐derived chemotaxin 2 as a biomarker of insulin resistance, liver enzymes, and metabolic dysfunction‐associated steatotic liver disease in the general populationKeita Suzuki0Hiromasa Tsujiguchi1Akinori Hara2Yumie Takeshita3Hisanori Goto4Yujiro Nakano5Reina Yamamoto6Hiroaki Takayama7Atsushi Tajima8Tatsuya Yamashita9Masao Honda10Hiroyuki Nakamura11Toshinari Takamura12Kanazawa University Advanced Preventive Medical Sciences Research Center Kanazawa Ishikawa JapanKanazawa University Advanced Preventive Medical Sciences Research Center Kanazawa Ishikawa JapanKanazawa University Advanced Preventive Medical Sciences Research Center Kanazawa Ishikawa JapanDepartment of Endocrinology and Metabolism Kanazawa University Graduate School of Medical Sciences Kanazawa Ishikawa JapanDepartment of Endocrinology and Metabolism Kanazawa University Graduate School of Medical Sciences Kanazawa Ishikawa JapanDepartment of Endocrinology and Metabolism Kanazawa University Graduate School of Medical Sciences Kanazawa Ishikawa JapanDepartment of Endocrinology and Metabolism Kanazawa University Graduate School of Medical Sciences Kanazawa Ishikawa JapanDepartment of Endocrinology and Metabolism Kanazawa University Graduate School of Medical Sciences Kanazawa Ishikawa JapanKanazawa University Advanced Preventive Medical Sciences Research Center Kanazawa Ishikawa JapanDepartment of Gastroenterology Kanazawa University Graduate School of Medical Sciences Kanazawa Ishikawa JapanDepartment of Gastroenterology Kanazawa University Graduate School of Medical Sciences Kanazawa Ishikawa JapanKanazawa University Advanced Preventive Medical Sciences Research Center Kanazawa Ishikawa JapanDepartment of Endocrinology and Metabolism Kanazawa University Graduate School of Medical Sciences Kanazawa Ishikawa JapanABSTRACT Aims/Introduction Leukocyte cell‐derived chemotaxin 2 (LECT2) is an obesity‐associated hepatokine that causes skeletal muscle insulin resistance. Since LECT2 is up‐regulated by the inactivation of the energy sensor AMPK in the liver, we hypothesized that LECT2 has potential as a biomarker for metabolic dysfunction‐associated steatotic liver disease (MASLD). Therefore, we investigated whether circulating LECT2 levels are associated with insulin sensitivity, liver enzymes, and MASLD. Materials and Methods This cross‐sectional study included 138 Japanese individuals. Plasma LECT2 levels were measured using fasting blood samples. B‐mode ultrasonography was used to assess hepatic steatosis. Results The mean age and body mass index (BMI) of participants were 63.5 ± 10.2 years and 23.0 ± 3.1 kg/m2, respectively. Higher LECT2 levels positively correlated with homeostatic model assessment for insulin resistance (HOMA‐IR) values and negatively correlated with the quantitative insulin sensitivity check index (QUICKI) among all participants (HOMA‐IR; non‐standardized β (B) = 6.38, P < 0.01: QUICKI; B = −161, P < 0.01). These correlations were stronger in the low BMI group (HOMA‐IR; B = 13.85, P < 0.01: QUICKI; B = −180, P < 0.01). LECT2 levels also positively correlated with gamma‐glutamyl transferase levels (B = 0.01, P = 0.01) and alanine aminotransferase levels (B = 0.33, P = 0.02). Higher LECT2 levels correlated with the prevalence of MASLD (odds ratio = 1.14, P = 0.02). Conclusions The present results suggest the potential of plasma LECT2 levels as a biomarker for insulin resistance in individuals who are not overweight and the prevalence of MASLD in the general population.https://doi.org/10.1111/jdi.14351Insulin resistanceLECT2MASLD
spellingShingle Keita Suzuki
Hiromasa Tsujiguchi
Akinori Hara
Yumie Takeshita
Hisanori Goto
Yujiro Nakano
Reina Yamamoto
Hiroaki Takayama
Atsushi Tajima
Tatsuya Yamashita
Masao Honda
Hiroyuki Nakamura
Toshinari Takamura
Hepatokine leukocyte cell‐derived chemotaxin 2 as a biomarker of insulin resistance, liver enzymes, and metabolic dysfunction‐associated steatotic liver disease in the general population
Journal of Diabetes Investigation
Insulin resistance
LECT2
MASLD
title Hepatokine leukocyte cell‐derived chemotaxin 2 as a biomarker of insulin resistance, liver enzymes, and metabolic dysfunction‐associated steatotic liver disease in the general population
title_full Hepatokine leukocyte cell‐derived chemotaxin 2 as a biomarker of insulin resistance, liver enzymes, and metabolic dysfunction‐associated steatotic liver disease in the general population
title_fullStr Hepatokine leukocyte cell‐derived chemotaxin 2 as a biomarker of insulin resistance, liver enzymes, and metabolic dysfunction‐associated steatotic liver disease in the general population
title_full_unstemmed Hepatokine leukocyte cell‐derived chemotaxin 2 as a biomarker of insulin resistance, liver enzymes, and metabolic dysfunction‐associated steatotic liver disease in the general population
title_short Hepatokine leukocyte cell‐derived chemotaxin 2 as a biomarker of insulin resistance, liver enzymes, and metabolic dysfunction‐associated steatotic liver disease in the general population
title_sort hepatokine leukocyte cell derived chemotaxin 2 as a biomarker of insulin resistance liver enzymes and metabolic dysfunction associated steatotic liver disease in the general population
topic Insulin resistance
LECT2
MASLD
url https://doi.org/10.1111/jdi.14351
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