Loading…
Sodium–glucose cotransporter 2 inhibitor‐induced changes in body composition and simultaneous changes in metabolic profile: 52‐week prospective LIGHT (Luseogliflozin: the Components of Weight Loss in Japanese Patients with Type 2 Diabetes Mellitus) Study
Aims/Introduction It is unclear how changes in body composition induced by sodium–glucose cotransporter 2 (SGLT2) inhibitor treatment correlate with metabolic profile changes. We aimed to clarify how metabolic profile changes correlate with body component changes, and if SGLT2 inhibitor treatment ca...
Saved in:
Published in: | Journal of diabetes investigation 2019-01, Vol.10 (1), p.108-117 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c6271-5a11bcaca59dc427c4aba0cadb711d2c00aee4dd9e3e98c6544fedbb7e4bf8e13 |
---|---|
cites | cdi_FETCH-LOGICAL-c6271-5a11bcaca59dc427c4aba0cadb711d2c00aee4dd9e3e98c6544fedbb7e4bf8e13 |
container_end_page | 117 |
container_issue | 1 |
container_start_page | 108 |
container_title | Journal of diabetes investigation |
container_volume | 10 |
creator | Sasaki, Takashi Sugawara, Masahiro Fukuda, Masahiro |
description | Aims/Introduction
It is unclear how changes in body composition induced by sodium–glucose cotransporter 2 (SGLT2) inhibitor treatment correlate with metabolic profile changes. We aimed to clarify how metabolic profile changes correlate with body component changes, and if SGLT2 inhibitor treatment causes sarcopenia and bone mineral content (BMC) loss.
Materials and Methods
Moderately obese Japanese type 2 diabetes patients, treated with luseogliflozin for a year, were observed prospectively and evaluated for body composition changes. We analyzed the changes in the individual body components during treatment, and their correlation with other clinical variables.
Results
The efficacy analysis set comprised 37 of 43 enrolled patients. The total fat mass significantly decreased early in the treatment at and after week 4, with a mean decrease of −1.97 kg (95% confidence interval −2.66 to −1.28) at week 24. The visceral fat area at week 24 showed an average downward trend, although this was not significant. The changes in visceral fat area in individual patients showed a significant negative correlation with the extent of the baseline visceral fat area (r = −0.399, P = 0.023). The skeletal muscle mass index showed a significant but small change at and after week 36. The BMC profile showed a transient significant decrease only at week 12. No significant change in BMC was noted at other time‐points.
Conclusions
Luseogliflozin treatment brought about favorable changes in body composition and metabolism of moderately obese Japanese type 2 diabetes patients, accompanied by body fat reduction, and minimal muscle and BMC reduction.
Luseogliflozin treatment was found to be capable of controlling T2D with favorable changes in the body composition and metabolism accompanied by minimal muscle and BMC reduction, even in moderately obese patients. The changes in the visceral fat area at Week 24 in individual patients showed a significant negative correlation with the respective visceral fat area levels at the baseline (r = −0.457, P = 0.0085). |
doi_str_mv | 10.1111/jdi.12851 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_8775fe4e338645c58be36928852b6948</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_8775fe4e338645c58be36928852b6948</doaj_id><sourcerecordid>2163026956</sourcerecordid><originalsourceid>FETCH-LOGICAL-c6271-5a11bcaca59dc427c4aba0cadb711d2c00aee4dd9e3e98c6544fedbb7e4bf8e13</originalsourceid><addsrcrecordid>eNp1ks1u1DAQxwMqolXpgRdAlrjQw7axkzhJD0hoC-1Wi0DqIo6WPyaJlyQOttPVcuojIPGGfRK8u6VqD8zF1sx_fjOjmSh6jeMTHOx0qfQJJkWGn0cHJE7jCcYk3Xv4Y7ofHTm3jIMlRUFp_jLaJyWlcV6Qg2d710bpsbu7_VO3ozQOkDTe8t4NxnqwiCDdN1pob-zd7W_dq1GCQrLhfQ0uxJAwah1yusE47bXpEe8VcrobW897MKN7LO7Ac2FaLdFgTaVbOEMZCdwVwI-Nyw0gvb4BNJ9dXC7Qu_nowNStrlrzS_dnyDeApptaPfTeIVOh76DrxqO5cdsCV3wIVcMUX7nXW81K-wYt1gOEUc41F-BDK5-hbbUf3TG69qNav4peVLx1cHT_HkbfPn1cTC8n8y8Xs-mH-URSkuNJxjEWkkuelUqmJJcpFzyWXIkcY0VkHHOAVKkSEigLSbM0rUAJkUMqqgJwchjNdlxl-JINVnfcrpnhmm0dxtaMW69lC6zI86yCFJKkoGkms0JAQktSFBkRtEyLwHq_Yw2j6EDJMKzl7RPo00ivG1abG0YTvMkPgLf3AGt-juA8W5rR9mF-RjBNYkLLjAbV8U4lw3acheqhAo7Z5v5YuD-2vb-gffO4pQflv2sLgtOdYBVWv_4_iV2dz3bIv_477fc</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2163026956</pqid></control><display><type>article</type><title>Sodium–glucose cotransporter 2 inhibitor‐induced changes in body composition and simultaneous changes in metabolic profile: 52‐week prospective LIGHT (Luseogliflozin: the Components of Weight Loss in Japanese Patients with Type 2 Diabetes Mellitus) Study</title><source>Publicly Available Content Database</source><source>Wiley Open Access</source><source>PubMed Central</source><creator>Sasaki, Takashi ; Sugawara, Masahiro ; Fukuda, Masahiro</creator><creatorcontrib>Sasaki, Takashi ; Sugawara, Masahiro ; Fukuda, Masahiro</creatorcontrib><description>Aims/Introduction
It is unclear how changes in body composition induced by sodium–glucose cotransporter 2 (SGLT2) inhibitor treatment correlate with metabolic profile changes. We aimed to clarify how metabolic profile changes correlate with body component changes, and if SGLT2 inhibitor treatment causes sarcopenia and bone mineral content (BMC) loss.
Materials and Methods
Moderately obese Japanese type 2 diabetes patients, treated with luseogliflozin for a year, were observed prospectively and evaluated for body composition changes. We analyzed the changes in the individual body components during treatment, and their correlation with other clinical variables.
Results
The efficacy analysis set comprised 37 of 43 enrolled patients. The total fat mass significantly decreased early in the treatment at and after week 4, with a mean decrease of −1.97 kg (95% confidence interval −2.66 to −1.28) at week 24. The visceral fat area at week 24 showed an average downward trend, although this was not significant. The changes in visceral fat area in individual patients showed a significant negative correlation with the extent of the baseline visceral fat area (r = −0.399, P = 0.023). The skeletal muscle mass index showed a significant but small change at and after week 36. The BMC profile showed a transient significant decrease only at week 12. No significant change in BMC was noted at other time‐points.
Conclusions
Luseogliflozin treatment brought about favorable changes in body composition and metabolism of moderately obese Japanese type 2 diabetes patients, accompanied by body fat reduction, and minimal muscle and BMC reduction.
Luseogliflozin treatment was found to be capable of controlling T2D with favorable changes in the body composition and metabolism accompanied by minimal muscle and BMC reduction, even in moderately obese patients. The changes in the visceral fat area at Week 24 in individual patients showed a significant negative correlation with the respective visceral fat area levels at the baseline (r = −0.457, P = 0.0085).</description><identifier>ISSN: 2040-1116</identifier><identifier>EISSN: 2040-1124</identifier><identifier>DOI: 10.1111/jdi.12851</identifier><identifier>PMID: 29660782</identifier><language>eng</language><publisher>Japan: John Wiley & Sons, Inc</publisher><subject>Asians ; Blood Glucose - drug effects ; Body composition ; Body Composition - drug effects ; Body fat ; Body weight loss ; Bone mineral content ; Diabetes ; Diabetes mellitus ; Diabetes mellitus (non-insulin dependent) ; Diabetes Mellitus, Type 2 - drug therapy ; Diabetes Mellitus, Type 2 - metabolism ; Dual‐energy X‐ray absorption ; Female ; Humans ; Hypoglycemic Agents - therapeutic use ; Intra-Abdominal Fat - metabolism ; Japan ; Male ; Metabolism ; Middle Aged ; Na+/glucose cotransporter ; Original ; Patients ; Prospective Studies ; Sarcopenia ; Skeletal muscle ; Sodium ; Sodium-Glucose Transporter 2 - metabolism ; Sodium-Glucose Transporter 2 Inhibitors - therapeutic use ; Sorbitol - analogs & derivatives ; Sorbitol - therapeutic use ; Visceral fat ; Weight Loss - drug effects</subject><ispartof>Journal of diabetes investigation, 2019-01, Vol.10 (1), p.108-117</ispartof><rights>2018 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd</rights><rights>2018 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd.</rights><rights>2019. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). 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><citedby>FETCH-LOGICAL-c6271-5a11bcaca59dc427c4aba0cadb711d2c00aee4dd9e3e98c6544fedbb7e4bf8e13</citedby><cites>FETCH-LOGICAL-c6271-5a11bcaca59dc427c4aba0cadb711d2c00aee4dd9e3e98c6544fedbb7e4bf8e13</cites><orcidid>0000-0002-1413-6983 ; 0000-0003-0172-8661</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2163026956/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2163026956?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11562,25753,27924,27925,37012,44590,46052,46476,53791,53793,74998</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29660782$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sasaki, Takashi</creatorcontrib><creatorcontrib>Sugawara, Masahiro</creatorcontrib><creatorcontrib>Fukuda, Masahiro</creatorcontrib><title>Sodium–glucose cotransporter 2 inhibitor‐induced changes in body composition and simultaneous changes in metabolic profile: 52‐week prospective LIGHT (Luseogliflozin: the Components of Weight Loss in Japanese Patients with Type 2 Diabetes Mellitus) Study</title><title>Journal of diabetes investigation</title><addtitle>J Diabetes Investig</addtitle><description>Aims/Introduction
It is unclear how changes in body composition induced by sodium–glucose cotransporter 2 (SGLT2) inhibitor treatment correlate with metabolic profile changes. We aimed to clarify how metabolic profile changes correlate with body component changes, and if SGLT2 inhibitor treatment causes sarcopenia and bone mineral content (BMC) loss.
Materials and Methods
Moderately obese Japanese type 2 diabetes patients, treated with luseogliflozin for a year, were observed prospectively and evaluated for body composition changes. We analyzed the changes in the individual body components during treatment, and their correlation with other clinical variables.
Results
The efficacy analysis set comprised 37 of 43 enrolled patients. The total fat mass significantly decreased early in the treatment at and after week 4, with a mean decrease of −1.97 kg (95% confidence interval −2.66 to −1.28) at week 24. The visceral fat area at week 24 showed an average downward trend, although this was not significant. The changes in visceral fat area in individual patients showed a significant negative correlation with the extent of the baseline visceral fat area (r = −0.399, P = 0.023). The skeletal muscle mass index showed a significant but small change at and after week 36. The BMC profile showed a transient significant decrease only at week 12. No significant change in BMC was noted at other time‐points.
Conclusions
Luseogliflozin treatment brought about favorable changes in body composition and metabolism of moderately obese Japanese type 2 diabetes patients, accompanied by body fat reduction, and minimal muscle and BMC reduction.
Luseogliflozin treatment was found to be capable of controlling T2D with favorable changes in the body composition and metabolism accompanied by minimal muscle and BMC reduction, even in moderately obese patients. The changes in the visceral fat area at Week 24 in individual patients showed a significant negative correlation with the respective visceral fat area levels at the baseline (r = −0.457, P = 0.0085).</description><subject>Asians</subject><subject>Blood Glucose - drug effects</subject><subject>Body composition</subject><subject>Body Composition - drug effects</subject><subject>Body fat</subject><subject>Body weight loss</subject><subject>Bone mineral content</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Diabetes Mellitus, Type 2 - drug therapy</subject><subject>Diabetes Mellitus, Type 2 - metabolism</subject><subject>Dual‐energy X‐ray absorption</subject><subject>Female</subject><subject>Humans</subject><subject>Hypoglycemic Agents - therapeutic use</subject><subject>Intra-Abdominal Fat - metabolism</subject><subject>Japan</subject><subject>Male</subject><subject>Metabolism</subject><subject>Middle Aged</subject><subject>Na+/glucose cotransporter</subject><subject>Original</subject><subject>Patients</subject><subject>Prospective Studies</subject><subject>Sarcopenia</subject><subject>Skeletal muscle</subject><subject>Sodium</subject><subject>Sodium-Glucose Transporter 2 - metabolism</subject><subject>Sodium-Glucose Transporter 2 Inhibitors - therapeutic use</subject><subject>Sorbitol - analogs & derivatives</subject><subject>Sorbitol - therapeutic use</subject><subject>Visceral fat</subject><subject>Weight Loss - drug effects</subject><issn>2040-1116</issn><issn>2040-1124</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1ks1u1DAQxwMqolXpgRdAlrjQw7axkzhJD0hoC-1Wi0DqIo6WPyaJlyQOttPVcuojIPGGfRK8u6VqD8zF1sx_fjOjmSh6jeMTHOx0qfQJJkWGn0cHJE7jCcYk3Xv4Y7ofHTm3jIMlRUFp_jLaJyWlcV6Qg2d710bpsbu7_VO3ozQOkDTe8t4NxnqwiCDdN1pob-zd7W_dq1GCQrLhfQ0uxJAwah1yusE47bXpEe8VcrobW897MKN7LO7Ac2FaLdFgTaVbOEMZCdwVwI-Nyw0gvb4BNJ9dXC7Qu_nowNStrlrzS_dnyDeApptaPfTeIVOh76DrxqO5cdsCV3wIVcMUX7nXW81K-wYt1gOEUc41F-BDK5-hbbUf3TG69qNav4peVLx1cHT_HkbfPn1cTC8n8y8Xs-mH-URSkuNJxjEWkkuelUqmJJcpFzyWXIkcY0VkHHOAVKkSEigLSbM0rUAJkUMqqgJwchjNdlxl-JINVnfcrpnhmm0dxtaMW69lC6zI86yCFJKkoGkms0JAQktSFBkRtEyLwHq_Yw2j6EDJMKzl7RPo00ivG1abG0YTvMkPgLf3AGt-juA8W5rR9mF-RjBNYkLLjAbV8U4lw3acheqhAo7Z5v5YuD-2vb-gffO4pQflv2sLgtOdYBVWv_4_iV2dz3bIv_477fc</recordid><startdate>201901</startdate><enddate>201901</enddate><creator>Sasaki, Takashi</creator><creator>Sugawara, Masahiro</creator><creator>Fukuda, Masahiro</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-1413-6983</orcidid><orcidid>https://orcid.org/0000-0003-0172-8661</orcidid></search><sort><creationdate>201901</creationdate><title>Sodium–glucose cotransporter 2 inhibitor‐induced changes in body composition and simultaneous changes in metabolic profile: 52‐week prospective LIGHT (Luseogliflozin: the Components of Weight Loss in Japanese Patients with Type 2 Diabetes Mellitus) Study</title><author>Sasaki, Takashi ; Sugawara, Masahiro ; Fukuda, Masahiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6271-5a11bcaca59dc427c4aba0cadb711d2c00aee4dd9e3e98c6544fedbb7e4bf8e13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Asians</topic><topic>Blood Glucose - drug effects</topic><topic>Body composition</topic><topic>Body Composition - drug effects</topic><topic>Body fat</topic><topic>Body weight loss</topic><topic>Bone mineral content</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Diabetes Mellitus, Type 2 - drug therapy</topic><topic>Diabetes Mellitus, Type 2 - metabolism</topic><topic>Dual‐energy X‐ray absorption</topic><topic>Female</topic><topic>Humans</topic><topic>Hypoglycemic Agents - therapeutic use</topic><topic>Intra-Abdominal Fat - metabolism</topic><topic>Japan</topic><topic>Male</topic><topic>Metabolism</topic><topic>Middle Aged</topic><topic>Na+/glucose cotransporter</topic><topic>Original</topic><topic>Patients</topic><topic>Prospective Studies</topic><topic>Sarcopenia</topic><topic>Skeletal muscle</topic><topic>Sodium</topic><topic>Sodium-Glucose Transporter 2 - metabolism</topic><topic>Sodium-Glucose Transporter 2 Inhibitors - therapeutic use</topic><topic>Sorbitol - analogs & derivatives</topic><topic>Sorbitol - therapeutic use</topic><topic>Visceral fat</topic><topic>Weight Loss - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sasaki, Takashi</creatorcontrib><creatorcontrib>Sugawara, Masahiro</creatorcontrib><creatorcontrib>Fukuda, Masahiro</creatorcontrib><collection>Wiley Open Access</collection><collection>Wiley-Blackwell Open Access Backfiles</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>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>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Journal of diabetes investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sasaki, Takashi</au><au>Sugawara, Masahiro</au><au>Fukuda, Masahiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sodium–glucose cotransporter 2 inhibitor‐induced changes in body composition and simultaneous changes in metabolic profile: 52‐week prospective LIGHT (Luseogliflozin: the Components of Weight Loss in Japanese Patients with Type 2 Diabetes Mellitus) Study</atitle><jtitle>Journal of diabetes investigation</jtitle><addtitle>J Diabetes Investig</addtitle><date>2019-01</date><risdate>2019</risdate><volume>10</volume><issue>1</issue><spage>108</spage><epage>117</epage><pages>108-117</pages><issn>2040-1116</issn><eissn>2040-1124</eissn><abstract>Aims/Introduction
It is unclear how changes in body composition induced by sodium–glucose cotransporter 2 (SGLT2) inhibitor treatment correlate with metabolic profile changes. We aimed to clarify how metabolic profile changes correlate with body component changes, and if SGLT2 inhibitor treatment causes sarcopenia and bone mineral content (BMC) loss.
Materials and Methods
Moderately obese Japanese type 2 diabetes patients, treated with luseogliflozin for a year, were observed prospectively and evaluated for body composition changes. We analyzed the changes in the individual body components during treatment, and their correlation with other clinical variables.
Results
The efficacy analysis set comprised 37 of 43 enrolled patients. The total fat mass significantly decreased early in the treatment at and after week 4, with a mean decrease of −1.97 kg (95% confidence interval −2.66 to −1.28) at week 24. The visceral fat area at week 24 showed an average downward trend, although this was not significant. The changes in visceral fat area in individual patients showed a significant negative correlation with the extent of the baseline visceral fat area (r = −0.399, P = 0.023). The skeletal muscle mass index showed a significant but small change at and after week 36. The BMC profile showed a transient significant decrease only at week 12. No significant change in BMC was noted at other time‐points.
Conclusions
Luseogliflozin treatment brought about favorable changes in body composition and metabolism of moderately obese Japanese type 2 diabetes patients, accompanied by body fat reduction, and minimal muscle and BMC reduction.
Luseogliflozin treatment was found to be capable of controlling T2D with favorable changes in the body composition and metabolism accompanied by minimal muscle and BMC reduction, even in moderately obese patients. The changes in the visceral fat area at Week 24 in individual patients showed a significant negative correlation with the respective visceral fat area levels at the baseline (r = −0.457, P = 0.0085).</abstract><cop>Japan</cop><pub>John Wiley & Sons, Inc</pub><pmid>29660782</pmid><doi>10.1111/jdi.12851</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-1413-6983</orcidid><orcidid>https://orcid.org/0000-0003-0172-8661</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2040-1116 |
ispartof | Journal of diabetes investigation, 2019-01, Vol.10 (1), p.108-117 |
issn | 2040-1116 2040-1124 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_8775fe4e338645c58be36928852b6948 |
source | Publicly Available Content Database; Wiley Open Access; PubMed Central |
subjects | Asians Blood Glucose - drug effects Body composition Body Composition - drug effects Body fat Body weight loss Bone mineral content Diabetes Diabetes mellitus Diabetes mellitus (non-insulin dependent) Diabetes Mellitus, Type 2 - drug therapy Diabetes Mellitus, Type 2 - metabolism Dual‐energy X‐ray absorption Female Humans Hypoglycemic Agents - therapeutic use Intra-Abdominal Fat - metabolism Japan Male Metabolism Middle Aged Na+/glucose cotransporter Original Patients Prospective Studies Sarcopenia Skeletal muscle Sodium Sodium-Glucose Transporter 2 - metabolism Sodium-Glucose Transporter 2 Inhibitors - therapeutic use Sorbitol - analogs & derivatives Sorbitol - therapeutic use Visceral fat Weight Loss - drug effects |
title | Sodium–glucose cotransporter 2 inhibitor‐induced changes in body composition and simultaneous changes in metabolic profile: 52‐week prospective LIGHT (Luseogliflozin: the Components of Weight Loss in Japanese Patients with Type 2 Diabetes Mellitus) Study |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T14%3A23%3A06IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Sodium%E2%80%93glucose%20cotransporter%202%20inhibitor%E2%80%90induced%20changes%20in%20body%20composition%20and%20simultaneous%20changes%20in%20metabolic%20profile:%2052%E2%80%90week%20prospective%20LIGHT%20(Luseogliflozin:%20the%20Components%20of%20Weight%20Loss%20in%20Japanese%20Patients%20with%20Type%202%20Diabetes%20Mellitus)%20Study&rft.jtitle=Journal%20of%20diabetes%20investigation&rft.au=Sasaki,%20Takashi&rft.date=2019-01&rft.volume=10&rft.issue=1&rft.spage=108&rft.epage=117&rft.pages=108-117&rft.issn=2040-1116&rft.eissn=2040-1124&rft_id=info:doi/10.1111/jdi.12851&rft_dat=%3Cproquest_doaj_%3E2163026956%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c6271-5a11bcaca59dc427c4aba0cadb711d2c00aee4dd9e3e98c6544fedbb7e4bf8e13%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2163026956&rft_id=info:pmid/29660782&rfr_iscdi=true |