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Abdominal fat depots and their association with insulin resistance in patients with type 2 diabetes
Asian-Indians show thin fat phenotype, characterized by predominantly central deposition of excess fat. The roles of abdominal subcutaneous fat (SAT), intra-peritoneal adipose tissue, and fat depots surrounding the vital organs (IPAT-SV) and liver fat in insulin resistance (IR), type-2 diabetes (T2D...
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Published in: | PloS one 2023-12, Vol.18 (12), p.e0295492-e0295492 |
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creator | Garg, Umesh Kumar Mathur, Nitish Sahlot, Rahul Tiwari, Pradeep Sharma, Balram Saxena, Aditya Jainaw, Raj Kamal Agarwal, Laxman Gupta, Shalu Mathur, Sandeep Kumar |
description | Asian-Indians show thin fat phenotype, characterized by predominantly central deposition of excess fat. The roles of abdominal subcutaneous fat (SAT), intra-peritoneal adipose tissue, and fat depots surrounding the vital organs (IPAT-SV) and liver fat in insulin resistance (IR), type-2 diabetes (T2D) and metabolic syndrome (MetS) in this population are sparsely investigated.
Assessment of liver fat, SAT and IPAT-SV by MRI in subjects with T2D and MetS; and to investigate its correlation with IR, specifically according to different quartiles of HOMA-IR.
Eighty T2D and the equal number of age sex-matched normal glucose tolerant controls participated in this study. Abdominal SAT, IPAT-SV and liver fat were measured using MRI. IR was estimated by the Homeostatic Model Assessment for Insulin Resistance (HOMA-IR).
T2D and MetS subjects have higher quantity liver fat and IPAT-SV fat than controls (P = 9 x 10-4 and 4 x 10-4 for T2D and 10-4 and 9 x 10-3 for MetS subjects respectively). MetS subjects also have higher SAT fat mass (P = 0.012), but not the BMI adjusted SAT fat mass (P = 0.48). Higher quartiles of HOMA-IR were associated with higher BMI, W:H ratio, waist circumference, and higher liver fat mass (ANOVA Test P = 0.020, 0.030, 2 x 10-6 and 3 x 10-3 respectively with F-values 3.35, 3.04, 8.82, 4.47 respectively). In T2D and MetS subjects, HOMA-IR showed a moderately strong correlation with liver fat (r = 0.467, P < 3 x 10-5 and r = 0.493, P < 10-7), but not with SAT fat and IPAT-SV. However, in MetS subjects IPAT-SV fat mass showed borderline correlation with IR (r = 0.241, P < 0.05), but not with the BMI adjusted IPAT-SV fat mass (r = 0.13, P = 0.26). In non-T2D and non-MetS subjects, no such correlation was seen. On analyzing the correlation between the three abdominal adipose compartment fat masses and IR according to its severity, the correlation with liver fat mass becomes stronger with increasing quartiles of HOMA-IR, and the strongest correlation is seen in the highest quartile (r = 0.59, P < 10-3). On the other hand, SAT fat mass tended to show an inverse relation with IR with borderline negative correlation in the highest quartile (r = -0.284, P < 0.05). IPAT-SV fat mass did not show any statistically significant correlation with HOMA-IR, but in the highest quartile it showed borderline, but statistically insignificant positive correlation (P = 0.07).
In individuals suffering from T2D and MetS, IR shows a trend towards positive and borderline neg |
doi_str_mv | 10.1371/journal.pone.0295492 |
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Assessment of liver fat, SAT and IPAT-SV by MRI in subjects with T2D and MetS; and to investigate its correlation with IR, specifically according to different quartiles of HOMA-IR.
Eighty T2D and the equal number of age sex-matched normal glucose tolerant controls participated in this study. Abdominal SAT, IPAT-SV and liver fat were measured using MRI. IR was estimated by the Homeostatic Model Assessment for Insulin Resistance (HOMA-IR).
T2D and MetS subjects have higher quantity liver fat and IPAT-SV fat than controls (P = 9 x 10-4 and 4 x 10-4 for T2D and 10-4 and 9 x 10-3 for MetS subjects respectively). MetS subjects also have higher SAT fat mass (P = 0.012), but not the BMI adjusted SAT fat mass (P = 0.48). Higher quartiles of HOMA-IR were associated with higher BMI, W:H ratio, waist circumference, and higher liver fat mass (ANOVA Test P = 0.020, 0.030, 2 x 10-6 and 3 x 10-3 respectively with F-values 3.35, 3.04, 8.82, 4.47 respectively). In T2D and MetS subjects, HOMA-IR showed a moderately strong correlation with liver fat (r = 0.467, P < 3 x 10-5 and r = 0.493, P < 10-7), but not with SAT fat and IPAT-SV. However, in MetS subjects IPAT-SV fat mass showed borderline correlation with IR (r = 0.241, P < 0.05), but not with the BMI adjusted IPAT-SV fat mass (r = 0.13, P = 0.26). In non-T2D and non-MetS subjects, no such correlation was seen. On analyzing the correlation between the three abdominal adipose compartment fat masses and IR according to its severity, the correlation with liver fat mass becomes stronger with increasing quartiles of HOMA-IR, and the strongest correlation is seen in the highest quartile (r = 0.59, P < 10-3). On the other hand, SAT fat mass tended to show an inverse relation with IR with borderline negative correlation in the highest quartile (r = -0.284, P < 0.05). IPAT-SV fat mass did not show any statistically significant correlation with HOMA-IR, but in the highest quartile it showed borderline, but statistically insignificant positive correlation (P = 0.07).
In individuals suffering from T2D and MetS, IR shows a trend towards positive and borderline negative correlation with liver fat and SAT fat masses respectively. The positive trend with liver fat tends to become stronger with increasing quartile of IR. Therefore, these findings support the theory that possibly exhaustion of protective compartment's capacity to store excess fat results in its pathological deposition in liver as ectopic fat.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0295492</identifier><identifier>PMID: 38064530</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Abdomen ; Abdominal Fat - diagnostic imaging ; Abdominal Fat - metabolism ; Adipose tissue ; Adipose tissues ; Automation ; Blood pressure ; Body fat ; Body Mass Index ; Care and treatment ; Cholesterol ; Complications and side effects ; Correlation ; Deposition ; Dextrose ; Diabetes ; Diabetes mellitus (non-insulin dependent) ; Diabetes Mellitus, Type 2 - metabolism ; Females ; Genotype & phenotype ; Glucose ; Health aspects ; High density lipoprotein ; Humans ; Insulin ; Insulin Resistance ; Lipoproteins ; Liver ; Magnetic resonance imaging ; Measurement ; Metabolic disorders ; Metabolic Syndrome ; Pathophysiology ; Phenotypes ; Prevention ; Quartiles ; Risk factors ; Software ; Spleen ; Statistical analysis ; Triglycerides ; Type 2 diabetes ; Variance analysis</subject><ispartof>PloS one, 2023-12, Vol.18 (12), p.e0295492-e0295492</ispartof><rights>Copyright: © 2023 Garg et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</rights><rights>COPYRIGHT 2023 Public Library of Science</rights><rights>2023 Garg et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 Garg et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c586t-d6317595f547f32834c5b4d00c7741e857ae718bf77fa7acaf6733c12f6f059f3</cites><orcidid>0000-0002-7402-2785 ; 0000-0001-7494-4061</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3072928596/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3072928596?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,25732,27903,27904,36991,36992,44569,74873</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38064530$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Mashili, Fredirick Lazaro</contributor><creatorcontrib>Garg, Umesh Kumar</creatorcontrib><creatorcontrib>Mathur, Nitish</creatorcontrib><creatorcontrib>Sahlot, Rahul</creatorcontrib><creatorcontrib>Tiwari, Pradeep</creatorcontrib><creatorcontrib>Sharma, Balram</creatorcontrib><creatorcontrib>Saxena, Aditya</creatorcontrib><creatorcontrib>Jainaw, Raj Kamal</creatorcontrib><creatorcontrib>Agarwal, Laxman</creatorcontrib><creatorcontrib>Gupta, Shalu</creatorcontrib><creatorcontrib>Mathur, Sandeep Kumar</creatorcontrib><title>Abdominal fat depots and their association with insulin resistance in patients with type 2 diabetes</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Asian-Indians show thin fat phenotype, characterized by predominantly central deposition of excess fat. The roles of abdominal subcutaneous fat (SAT), intra-peritoneal adipose tissue, and fat depots surrounding the vital organs (IPAT-SV) and liver fat in insulin resistance (IR), type-2 diabetes (T2D) and metabolic syndrome (MetS) in this population are sparsely investigated.
Assessment of liver fat, SAT and IPAT-SV by MRI in subjects with T2D and MetS; and to investigate its correlation with IR, specifically according to different quartiles of HOMA-IR.
Eighty T2D and the equal number of age sex-matched normal glucose tolerant controls participated in this study. Abdominal SAT, IPAT-SV and liver fat were measured using MRI. IR was estimated by the Homeostatic Model Assessment for Insulin Resistance (HOMA-IR).
T2D and MetS subjects have higher quantity liver fat and IPAT-SV fat than controls (P = 9 x 10-4 and 4 x 10-4 for T2D and 10-4 and 9 x 10-3 for MetS subjects respectively). MetS subjects also have higher SAT fat mass (P = 0.012), but not the BMI adjusted SAT fat mass (P = 0.48). Higher quartiles of HOMA-IR were associated with higher BMI, W:H ratio, waist circumference, and higher liver fat mass (ANOVA Test P = 0.020, 0.030, 2 x 10-6 and 3 x 10-3 respectively with F-values 3.35, 3.04, 8.82, 4.47 respectively). In T2D and MetS subjects, HOMA-IR showed a moderately strong correlation with liver fat (r = 0.467, P < 3 x 10-5 and r = 0.493, P < 10-7), but not with SAT fat and IPAT-SV. However, in MetS subjects IPAT-SV fat mass showed borderline correlation with IR (r = 0.241, P < 0.05), but not with the BMI adjusted IPAT-SV fat mass (r = 0.13, P = 0.26). In non-T2D and non-MetS subjects, no such correlation was seen. On analyzing the correlation between the three abdominal adipose compartment fat masses and IR according to its severity, the correlation with liver fat mass becomes stronger with increasing quartiles of HOMA-IR, and the strongest correlation is seen in the highest quartile (r = 0.59, P < 10-3). On the other hand, SAT fat mass tended to show an inverse relation with IR with borderline negative correlation in the highest quartile (r = -0.284, P < 0.05). IPAT-SV fat mass did not show any statistically significant correlation with HOMA-IR, but in the highest quartile it showed borderline, but statistically insignificant positive correlation (P = 0.07).
In individuals suffering from T2D and MetS, IR shows a trend towards positive and borderline negative correlation with liver fat and SAT fat masses respectively. The positive trend with liver fat tends to become stronger with increasing quartile of IR. Therefore, these findings support the theory that possibly exhaustion of protective compartment's capacity to store excess fat results in its pathological deposition in liver as ectopic fat.</description><subject>Abdomen</subject><subject>Abdominal Fat - diagnostic imaging</subject><subject>Abdominal Fat - metabolism</subject><subject>Adipose tissue</subject><subject>Adipose tissues</subject><subject>Automation</subject><subject>Blood pressure</subject><subject>Body fat</subject><subject>Body Mass Index</subject><subject>Care and treatment</subject><subject>Cholesterol</subject><subject>Complications and side effects</subject><subject>Correlation</subject><subject>Deposition</subject><subject>Dextrose</subject><subject>Diabetes</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Diabetes Mellitus, Type 2 - metabolism</subject><subject>Females</subject><subject>Genotype & phenotype</subject><subject>Glucose</subject><subject>Health aspects</subject><subject>High density lipoprotein</subject><subject>Humans</subject><subject>Insulin</subject><subject>Insulin Resistance</subject><subject>Lipoproteins</subject><subject>Liver</subject><subject>Magnetic resonance imaging</subject><subject>Measurement</subject><subject>Metabolic disorders</subject><subject>Metabolic Syndrome</subject><subject>Pathophysiology</subject><subject>Phenotypes</subject><subject>Prevention</subject><subject>Quartiles</subject><subject>Risk factors</subject><subject>Software</subject><subject>Spleen</subject><subject>Statistical analysis</subject><subject>Triglycerides</subject><subject>Type 2 diabetes</subject><subject>Variance 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fat depots and their association with insulin resistance in patients with type 2 diabetes</title><author>Garg, Umesh Kumar ; Mathur, Nitish ; Sahlot, Rahul ; Tiwari, Pradeep ; Sharma, Balram ; Saxena, Aditya ; Jainaw, Raj Kamal ; Agarwal, Laxman ; Gupta, Shalu ; Mathur, Sandeep Kumar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c586t-d6317595f547f32834c5b4d00c7741e857ae718bf77fa7acaf6733c12f6f059f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Abdomen</topic><topic>Abdominal Fat - diagnostic imaging</topic><topic>Abdominal Fat - metabolism</topic><topic>Adipose tissue</topic><topic>Adipose tissues</topic><topic>Automation</topic><topic>Blood pressure</topic><topic>Body fat</topic><topic>Body Mass Index</topic><topic>Care and treatment</topic><topic>Cholesterol</topic><topic>Complications and side 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Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>Engineering Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest advanced technologies & aerospace journals</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials science collection</collection><collection>ProQuest - Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Garg, Umesh Kumar</au><au>Mathur, Nitish</au><au>Sahlot, Rahul</au><au>Tiwari, Pradeep</au><au>Sharma, Balram</au><au>Saxena, Aditya</au><au>Jainaw, Raj Kamal</au><au>Agarwal, Laxman</au><au>Gupta, Shalu</au><au>Mathur, Sandeep Kumar</au><au>Mashili, Fredirick Lazaro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Abdominal fat depots and their association with insulin resistance in patients with type 2 diabetes</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2023-12-08</date><risdate>2023</risdate><volume>18</volume><issue>12</issue><spage>e0295492</spage><epage>e0295492</epage><pages>e0295492-e0295492</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Asian-Indians show thin fat phenotype, characterized by predominantly central deposition of excess fat. The roles of abdominal subcutaneous fat (SAT), intra-peritoneal adipose tissue, and fat depots surrounding the vital organs (IPAT-SV) and liver fat in insulin resistance (IR), type-2 diabetes (T2D) and metabolic syndrome (MetS) in this population are sparsely investigated.
Assessment of liver fat, SAT and IPAT-SV by MRI in subjects with T2D and MetS; and to investigate its correlation with IR, specifically according to different quartiles of HOMA-IR.
Eighty T2D and the equal number of age sex-matched normal glucose tolerant controls participated in this study. Abdominal SAT, IPAT-SV and liver fat were measured using MRI. IR was estimated by the Homeostatic Model Assessment for Insulin Resistance (HOMA-IR).
T2D and MetS subjects have higher quantity liver fat and IPAT-SV fat than controls (P = 9 x 10-4 and 4 x 10-4 for T2D and 10-4 and 9 x 10-3 for MetS subjects respectively). MetS subjects also have higher SAT fat mass (P = 0.012), but not the BMI adjusted SAT fat mass (P = 0.48). Higher quartiles of HOMA-IR were associated with higher BMI, W:H ratio, waist circumference, and higher liver fat mass (ANOVA Test P = 0.020, 0.030, 2 x 10-6 and 3 x 10-3 respectively with F-values 3.35, 3.04, 8.82, 4.47 respectively). In T2D and MetS subjects, HOMA-IR showed a moderately strong correlation with liver fat (r = 0.467, P < 3 x 10-5 and r = 0.493, P < 10-7), but not with SAT fat and IPAT-SV. However, in MetS subjects IPAT-SV fat mass showed borderline correlation with IR (r = 0.241, P < 0.05), but not with the BMI adjusted IPAT-SV fat mass (r = 0.13, P = 0.26). In non-T2D and non-MetS subjects, no such correlation was seen. On analyzing the correlation between the three abdominal adipose compartment fat masses and IR according to its severity, the correlation with liver fat mass becomes stronger with increasing quartiles of HOMA-IR, and the strongest correlation is seen in the highest quartile (r = 0.59, P < 10-3). On the other hand, SAT fat mass tended to show an inverse relation with IR with borderline negative correlation in the highest quartile (r = -0.284, P < 0.05). IPAT-SV fat mass did not show any statistically significant correlation with HOMA-IR, but in the highest quartile it showed borderline, but statistically insignificant positive correlation (P = 0.07).
In individuals suffering from T2D and MetS, IR shows a trend towards positive and borderline negative correlation with liver fat and SAT fat masses respectively. The positive trend with liver fat tends to become stronger with increasing quartile of IR. Therefore, these findings support the theory that possibly exhaustion of protective compartment's capacity to store excess fat results in its pathological deposition in liver as ectopic fat.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>38064530</pmid><doi>10.1371/journal.pone.0295492</doi><tpages>e0295492</tpages><orcidid>https://orcid.org/0000-0002-7402-2785</orcidid><orcidid>https://orcid.org/0000-0001-7494-4061</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2023-12, Vol.18 (12), p.e0295492-e0295492 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_3072928596 |
source | Open Access: PubMed Central; ProQuest - Publicly Available Content Database |
subjects | Abdomen Abdominal Fat - diagnostic imaging Abdominal Fat - metabolism Adipose tissue Adipose tissues Automation Blood pressure Body fat Body Mass Index Care and treatment Cholesterol Complications and side effects Correlation Deposition Dextrose Diabetes Diabetes mellitus (non-insulin dependent) Diabetes Mellitus, Type 2 - metabolism Females Genotype & phenotype Glucose Health aspects High density lipoprotein Humans Insulin Insulin Resistance Lipoproteins Liver Magnetic resonance imaging Measurement Metabolic disorders Metabolic Syndrome Pathophysiology Phenotypes Prevention Quartiles Risk factors Software Spleen Statistical analysis Triglycerides Type 2 diabetes Variance analysis |
title | Abdominal fat depots and their association with insulin resistance in patients with type 2 diabetes |
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