Dysregulation of adipokines levels among healthy first-degree relatives of type 2 diabetes patients

Background: Leptin, adiponectin and its ratio (L/A), as well as adipocyte fatty acid binding protein (A-FABP) have shown association to type 2 diabetes and atherosclerosis. Since first degree relatives (FDR) of type 2 diabetes are known to have higher risks of developing aforementioned diseases, thi...

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Main Authors: Dyah Purnamasari, Cindya Klarisa Simanjuntak, Christian Tricaesario, Dicky Levenus Tahapary, Dante Saksono Harbuwono, Em Yunir
Format: Article
Language:English
Published: Elsevier 2023-08-01
Series:Heliyon
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2405844023060954
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author Dyah Purnamasari
Cindya Klarisa Simanjuntak
Christian Tricaesario
Dicky Levenus Tahapary
Dante Saksono Harbuwono
Em Yunir
author_facet Dyah Purnamasari
Cindya Klarisa Simanjuntak
Christian Tricaesario
Dicky Levenus Tahapary
Dante Saksono Harbuwono
Em Yunir
author_sort Dyah Purnamasari
collection DOAJ
description Background: Leptin, adiponectin and its ratio (L/A), as well as adipocyte fatty acid binding protein (A-FABP) have shown association to type 2 diabetes and atherosclerosis. Since first degree relatives (FDR) of type 2 diabetes are known to have higher risks of developing aforementioned diseases, this study aimed to see differences in adipokines profiles between FDR of type 2 diabetes and non-FDR counterpart. Methods: Age, sex and body mass index (BMI)-matched normotensive-normoglycemic subjects, aged 19–39 years with BMI<30 kg/m2, were included in this cross-sectional study. Serum adiponectin, leptin, and A-FABP levels were measured by sandwich ELISA while HOMA-IR was calculated from fasting blood glucose and insulin levels. Results: Of 116 subjects recruited, there were significant difference of insulin level (6.00 vs 5.00 μIU/mL, P = 0.029) and HOMA-IR (1.27 vs 1.10, P = 0.028). Adiponectin, leptin, L/A ratio, and A-FABP levels were not statistically different between FDR and non-FDR groups. Stratified by BMI, non-obese FDR had higher L/A ratio (0.83 vs 0.49, P = 0.020) compared to those of corresponding non-FDR. In multivariate analysis, after adjusting for age, sex, waist circumference, BMI, and metabolic profiles (HbA1C, HOMA-IR, LDL-C, HDL-C, and triglyceride levels), FDR status became significantly associated with adiponectin level, and in non-obese subgroup, remained its significance with L/A ratio. Conclusion: The FDR status was independently associated with adiponectin level. Furthermore, higher L/A ratio was more pronounced in non-obese FDR than those of non-FDR subjects, suggesting that FDR status may already contribute to the development of adipokines dysregulation before obesity occurs.
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spelling doaj.art-3d92afd9136e409eae9364f687ef64e92023-08-30T05:52:59ZengElsevierHeliyon2405-84402023-08-0198e18887Dysregulation of adipokines levels among healthy first-degree relatives of type 2 diabetes patientsDyah Purnamasari0Cindya Klarisa Simanjuntak1Christian Tricaesario2Dicky Levenus Tahapary3Dante Saksono Harbuwono4Em Yunir5Division of Endocrinology Metabolism and Diabetes, Department of Internal Medicine, Dr. Cipto Mangunkusumo National Referral Hospital, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia; Metabolic Disorder, Cardiovascular and Aging Research Center, The Indonesian Medical Education and Research Institute, Faculty of Medicine Universitas Indonesia, Jakarta, Indonesia; Corresponding author. Division of Endocrinology Metabolism and Diabetes, Department of Internal Medicine, Dr. Cipto Mangunkusumo National Referral Hospital, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.Department of Internal Medicine, Dr. Cipto Mangunkusumo National Referral Hospital, Faculty of Medicine, Universitas Indonesia, Jakarta, IndonesiaMetabolic Disorder, Cardiovascular and Aging Research Center, The Indonesian Medical Education and Research Institute, Faculty of Medicine Universitas Indonesia, Jakarta, IndonesiaDivision of Endocrinology Metabolism and Diabetes, Department of Internal Medicine, Dr. Cipto Mangunkusumo National Referral Hospital, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia; Metabolic Disorder, Cardiovascular and Aging Research Center, The Indonesian Medical Education and Research Institute, Faculty of Medicine Universitas Indonesia, Jakarta, IndonesiaDivision of Endocrinology Metabolism and Diabetes, Department of Internal Medicine, Dr. Cipto Mangunkusumo National Referral Hospital, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia; Metabolic Disorder, Cardiovascular and Aging Research Center, The Indonesian Medical Education and Research Institute, Faculty of Medicine Universitas Indonesia, Jakarta, IndonesiaDivision of Endocrinology Metabolism and Diabetes, Department of Internal Medicine, Dr. Cipto Mangunkusumo National Referral Hospital, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia; Metabolic Disorder, Cardiovascular and Aging Research Center, The Indonesian Medical Education and Research Institute, Faculty of Medicine Universitas Indonesia, Jakarta, IndonesiaBackground: Leptin, adiponectin and its ratio (L/A), as well as adipocyte fatty acid binding protein (A-FABP) have shown association to type 2 diabetes and atherosclerosis. Since first degree relatives (FDR) of type 2 diabetes are known to have higher risks of developing aforementioned diseases, this study aimed to see differences in adipokines profiles between FDR of type 2 diabetes and non-FDR counterpart. Methods: Age, sex and body mass index (BMI)-matched normotensive-normoglycemic subjects, aged 19–39 years with BMI<30 kg/m2, were included in this cross-sectional study. Serum adiponectin, leptin, and A-FABP levels were measured by sandwich ELISA while HOMA-IR was calculated from fasting blood glucose and insulin levels. Results: Of 116 subjects recruited, there were significant difference of insulin level (6.00 vs 5.00 μIU/mL, P = 0.029) and HOMA-IR (1.27 vs 1.10, P = 0.028). Adiponectin, leptin, L/A ratio, and A-FABP levels were not statistically different between FDR and non-FDR groups. Stratified by BMI, non-obese FDR had higher L/A ratio (0.83 vs 0.49, P = 0.020) compared to those of corresponding non-FDR. In multivariate analysis, after adjusting for age, sex, waist circumference, BMI, and metabolic profiles (HbA1C, HOMA-IR, LDL-C, HDL-C, and triglyceride levels), FDR status became significantly associated with adiponectin level, and in non-obese subgroup, remained its significance with L/A ratio. Conclusion: The FDR status was independently associated with adiponectin level. Furthermore, higher L/A ratio was more pronounced in non-obese FDR than those of non-FDR subjects, suggesting that FDR status may already contribute to the development of adipokines dysregulation before obesity occurs.http://www.sciencedirect.com/science/article/pii/S2405844023060954Family historyInsulin resistanceLeptinAdiponectinAdipokinesType 2 diabetes mellitus
spellingShingle Dyah Purnamasari
Cindya Klarisa Simanjuntak
Christian Tricaesario
Dicky Levenus Tahapary
Dante Saksono Harbuwono
Em Yunir
Dysregulation of adipokines levels among healthy first-degree relatives of type 2 diabetes patients
Heliyon
Family history
Insulin resistance
Leptin
Adiponectin
Adipokines
Type 2 diabetes mellitus
title Dysregulation of adipokines levels among healthy first-degree relatives of type 2 diabetes patients
title_full Dysregulation of adipokines levels among healthy first-degree relatives of type 2 diabetes patients
title_fullStr Dysregulation of adipokines levels among healthy first-degree relatives of type 2 diabetes patients
title_full_unstemmed Dysregulation of adipokines levels among healthy first-degree relatives of type 2 diabetes patients
title_short Dysregulation of adipokines levels among healthy first-degree relatives of type 2 diabetes patients
title_sort dysregulation of adipokines levels among healthy first degree relatives of type 2 diabetes patients
topic Family history
Insulin resistance
Leptin
Adiponectin
Adipokines
Type 2 diabetes mellitus
url http://www.sciencedirect.com/science/article/pii/S2405844023060954
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