Underestimation of impaired glucose tolerance and usefulness of a continuous glucose monitoring system in chronic liver disease

Background and Aim The prevalence of glucose intolerance in chronic liver disease patients is high, but glucose intolerance may be overlooked in a single blood test. The purpose of this study is to evaluate blood glucose variability in patients with chronic liver disease by a continuous glucose moni...

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Veröffentlicht in:Journal of gastroenterology and hepatology 2022-03, Vol.37 (3), p.592-599
Hauptverfasser: Ogawa, Yutaro, Nakahara, Takashi, Ono, Masafumi, Kawaguchi, Takumi, Isoda, Hiroshi, Hiramatsu, Akira, Uchikawa, Shinsuke, Fujino, Hatsue, Murakami, Eisuke, Kawaoka, Tomokazu, Yamauchi, Masami, Tsuge, Masataka, Munekage, Kensuke, Ochi, Tsunehiro, Hayes, C Nelson, Imamura, Michio, Aikata, Hiroshi, Takahashi, Hirokazu, Torimura, Takuji, Chayama, Kazuaki
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container_issue 3
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container_title Journal of gastroenterology and hepatology
container_volume 37
creator Ogawa, Yutaro
Nakahara, Takashi
Ono, Masafumi
Kawaguchi, Takumi
Isoda, Hiroshi
Hiramatsu, Akira
Uchikawa, Shinsuke
Fujino, Hatsue
Murakami, Eisuke
Kawaoka, Tomokazu
Yamauchi, Masami
Tsuge, Masataka
Munekage, Kensuke
Ochi, Tsunehiro
Hayes, C Nelson
Imamura, Michio
Aikata, Hiroshi
Takahashi, Hirokazu
Torimura, Takuji
Chayama, Kazuaki
description Background and Aim The prevalence of glucose intolerance in chronic liver disease patients is high, but glucose intolerance may be overlooked in a single blood test. The purpose of this study is to evaluate blood glucose variability in patients with chronic liver disease by a continuous glucose monitoring system (CGMS) and to examine the discrepancy between hemoglobin A1c (HbA1c) levels estimated from average blood glucose levels and HbA1c. Methods This study included 335 patients with chronic liver disease associated with glucose intolerance. A fasting blood test and 72‐h CGMS were performed. The estimated HbA1c was calculated from the average blood glucose level, and the correlation between hepatic functional reserve and blood glucose‐related parameters was analyzed. From the obtained data, we created a new formula to calculate HbA1c without using CGMS. Results As hepatic functional reserve decreased, average blood glucose and insulin resistance increased while HbA1c decreased (P 
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The purpose of this study is to evaluate blood glucose variability in patients with chronic liver disease by a continuous glucose monitoring system (CGMS) and to examine the discrepancy between hemoglobin A1c (HbA1c) levels estimated from average blood glucose levels and HbA1c. Methods This study included 335 patients with chronic liver disease associated with glucose intolerance. A fasting blood test and 72‐h CGMS were performed. The estimated HbA1c was calculated from the average blood glucose level, and the correlation between hepatic functional reserve and blood glucose‐related parameters was analyzed. From the obtained data, we created a new formula to calculate HbA1c without using CGMS. Results As hepatic functional reserve decreased, average blood glucose and insulin resistance increased while HbA1c decreased (P &lt; 0.0001). The discrepancy between the estimated HbA1c calculated from the mean blood glucose level and the serum HbA1c (ΔHbA1c) increased as the liver reserve decreased. Using multiple regression analysis, a formula based on fasting blood glucose, HbA1c, body mass index, albumin, and liver function was constructed, and its validity was demonstrated in a study using a different control group. Conclusions Hemoglobin A1c may be underestimated because of decreased hepatic functional reserve. CGMS was useful in assessing accurate glycemic control of blood glucose and in detecting postprandial hyperglycemia and nocturnal hypoglycemia. Patients with chronic hepatic impairment should be corrected for hepatic functional reserve before glycemic control.</description><identifier>ISSN: 0815-9319</identifier><identifier>EISSN: 1440-1746</identifier><identifier>DOI: 10.1111/jgh.15766</identifier><identifier>PMID: 34928509</identifier><language>eng</language><publisher>Australia: Wiley Subscription Services, Inc</publisher><subject>Blood glucose ; Blood tests ; Body mass index ; Chromium ; Chronic Disease ; Continuous glucose monitoring system (CGMS) ; Glucose ; Glucose Intolerance - diagnosis ; Glucose Intolerance - epidemiology ; Glucose monitoring ; Glucose tolerance ; Glycated Hemoglobin A - analysis ; HbA1c ; Hemoglobin ; Humans ; Hyperglycemia ; Hypoglycemia ; Insulin ; Insulin resistance ; Intolerance ; Liver cirrhosis ; Liver cirrhosis (LC) ; Liver diseases ; Liver Diseases - blood ; Monitoring systems ; Monitoring, Physiologic ; Multiple regression analysis</subject><ispartof>Journal of gastroenterology and hepatology, 2022-03, Vol.37 (3), p.592-599</ispartof><rights>2021 Journal of Gastroenterology and Hepatology Foundation and John Wiley &amp; Sons Australia, Ltd</rights><rights>2021 Journal of Gastroenterology and Hepatology Foundation and John Wiley &amp; Sons Australia, Ltd.</rights><rights>2022 Journal of Gastroenterology and Hepatology Foundation and John Wiley &amp; Sons Australia, Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4086-3587307ee9cc2a7aaa7b0a8615e6649a051568cbb24782bb6e58107dcf3537b93</citedby><cites>FETCH-LOGICAL-c4086-3587307ee9cc2a7aaa7b0a8615e6649a051568cbb24782bb6e58107dcf3537b93</cites><orcidid>0000-0001-7762-4629 ; 0000-0002-2374-2889 ; 0000-0002-1538-4946 ; 0000-0002-5530-5341 ; 0000-0002-7064-4325 ; 0000-0003-0357-2795 ; 0000-0002-0745-991X ; 0000-0002-8549-6492 ; 0000-0002-3475-5802</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjgh.15766$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjgh.15766$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34928509$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ogawa, Yutaro</creatorcontrib><creatorcontrib>Nakahara, Takashi</creatorcontrib><creatorcontrib>Ono, Masafumi</creatorcontrib><creatorcontrib>Kawaguchi, Takumi</creatorcontrib><creatorcontrib>Isoda, Hiroshi</creatorcontrib><creatorcontrib>Hiramatsu, Akira</creatorcontrib><creatorcontrib>Uchikawa, Shinsuke</creatorcontrib><creatorcontrib>Fujino, Hatsue</creatorcontrib><creatorcontrib>Murakami, Eisuke</creatorcontrib><creatorcontrib>Kawaoka, Tomokazu</creatorcontrib><creatorcontrib>Yamauchi, Masami</creatorcontrib><creatorcontrib>Tsuge, Masataka</creatorcontrib><creatorcontrib>Munekage, Kensuke</creatorcontrib><creatorcontrib>Ochi, Tsunehiro</creatorcontrib><creatorcontrib>Hayes, C Nelson</creatorcontrib><creatorcontrib>Imamura, Michio</creatorcontrib><creatorcontrib>Aikata, Hiroshi</creatorcontrib><creatorcontrib>Takahashi, Hirokazu</creatorcontrib><creatorcontrib>Torimura, Takuji</creatorcontrib><creatorcontrib>Chayama, Kazuaki</creatorcontrib><title>Underestimation of impaired glucose tolerance and usefulness of a continuous glucose monitoring system in chronic liver disease</title><title>Journal of gastroenterology and hepatology</title><addtitle>J Gastroenterol Hepatol</addtitle><description>Background and Aim The prevalence of glucose intolerance in chronic liver disease patients is high, but glucose intolerance may be overlooked in a single blood test. The purpose of this study is to evaluate blood glucose variability in patients with chronic liver disease by a continuous glucose monitoring system (CGMS) and to examine the discrepancy between hemoglobin A1c (HbA1c) levels estimated from average blood glucose levels and HbA1c. Methods This study included 335 patients with chronic liver disease associated with glucose intolerance. A fasting blood test and 72‐h CGMS were performed. The estimated HbA1c was calculated from the average blood glucose level, and the correlation between hepatic functional reserve and blood glucose‐related parameters was analyzed. From the obtained data, we created a new formula to calculate HbA1c without using CGMS. Results As hepatic functional reserve decreased, average blood glucose and insulin resistance increased while HbA1c decreased (P &lt; 0.0001). The discrepancy between the estimated HbA1c calculated from the mean blood glucose level and the serum HbA1c (ΔHbA1c) increased as the liver reserve decreased. Using multiple regression analysis, a formula based on fasting blood glucose, HbA1c, body mass index, albumin, and liver function was constructed, and its validity was demonstrated in a study using a different control group. Conclusions Hemoglobin A1c may be underestimated because of decreased hepatic functional reserve. CGMS was useful in assessing accurate glycemic control of blood glucose and in detecting postprandial hyperglycemia and nocturnal hypoglycemia. Patients with chronic hepatic impairment should be corrected for hepatic functional reserve before glycemic control.</description><subject>Blood glucose</subject><subject>Blood tests</subject><subject>Body mass index</subject><subject>Chromium</subject><subject>Chronic Disease</subject><subject>Continuous glucose monitoring system (CGMS)</subject><subject>Glucose</subject><subject>Glucose Intolerance - diagnosis</subject><subject>Glucose Intolerance - epidemiology</subject><subject>Glucose monitoring</subject><subject>Glucose tolerance</subject><subject>Glycated Hemoglobin A - analysis</subject><subject>HbA1c</subject><subject>Hemoglobin</subject><subject>Humans</subject><subject>Hyperglycemia</subject><subject>Hypoglycemia</subject><subject>Insulin</subject><subject>Insulin resistance</subject><subject>Intolerance</subject><subject>Liver cirrhosis</subject><subject>Liver cirrhosis (LC)</subject><subject>Liver diseases</subject><subject>Liver Diseases - blood</subject><subject>Monitoring systems</subject><subject>Monitoring, Physiologic</subject><subject>Multiple regression analysis</subject><issn>0815-9319</issn><issn>1440-1746</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10c1O3DAUBWALFcFAu-gLVJa6gUXgOvFflhWiQ9FIbGAdOc7N4FFiT-2k1ax4dTwdyqJSvbFkfT669iHkM4Mrltf1Zv18xYSS8ogsGOdQMMXlB7IAzURRV6w-JWcpbQCAgxIn5LTidakF1Avy8uQ7jJgmN5rJBU9DT924NS5iR9fDbENCOoUBo_EWqfEdnRP28-AxpT021AY_OT-HOb1fGIN3U4jOr2napQlH6jy1zzEfWzq4Xxhp5xKahB_JcW-GhJ_e9nPy9P328eauWD0sf9x8WxWWg5ZFJbSqQCHW1pZGGWNUC0ZLJlBKXhsQTEht27bkSpdtK1FoBqqzfSUq1dbVObk45G5j-Dnn9zajSxaHwXjMkzelZCXwEoTO9Os_dBPm6PN0WVUKdM34Xl0elI0hpYh9s435D-OuYdDsW2lyK82fVrL98pY4tyN27_JvDRlcH8BvN-Du_0nN_fLuEPkKDnaYHg</recordid><startdate>202203</startdate><enddate>202203</enddate><creator>Ogawa, Yutaro</creator><creator>Nakahara, Takashi</creator><creator>Ono, Masafumi</creator><creator>Kawaguchi, Takumi</creator><creator>Isoda, Hiroshi</creator><creator>Hiramatsu, Akira</creator><creator>Uchikawa, Shinsuke</creator><creator>Fujino, Hatsue</creator><creator>Murakami, Eisuke</creator><creator>Kawaoka, Tomokazu</creator><creator>Yamauchi, Masami</creator><creator>Tsuge, Masataka</creator><creator>Munekage, Kensuke</creator><creator>Ochi, Tsunehiro</creator><creator>Hayes, C Nelson</creator><creator>Imamura, Michio</creator><creator>Aikata, Hiroshi</creator><creator>Takahashi, Hirokazu</creator><creator>Torimura, Takuji</creator><creator>Chayama, Kazuaki</creator><general>Wiley Subscription Services, Inc</general><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>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7762-4629</orcidid><orcidid>https://orcid.org/0000-0002-2374-2889</orcidid><orcidid>https://orcid.org/0000-0002-1538-4946</orcidid><orcidid>https://orcid.org/0000-0002-5530-5341</orcidid><orcidid>https://orcid.org/0000-0002-7064-4325</orcidid><orcidid>https://orcid.org/0000-0003-0357-2795</orcidid><orcidid>https://orcid.org/0000-0002-0745-991X</orcidid><orcidid>https://orcid.org/0000-0002-8549-6492</orcidid><orcidid>https://orcid.org/0000-0002-3475-5802</orcidid></search><sort><creationdate>202203</creationdate><title>Underestimation of impaired glucose tolerance and usefulness of a continuous glucose monitoring system in chronic liver disease</title><author>Ogawa, Yutaro ; Nakahara, Takashi ; Ono, Masafumi ; Kawaguchi, Takumi ; Isoda, Hiroshi ; Hiramatsu, Akira ; Uchikawa, Shinsuke ; Fujino, Hatsue ; Murakami, Eisuke ; Kawaoka, Tomokazu ; Yamauchi, Masami ; Tsuge, Masataka ; Munekage, Kensuke ; Ochi, Tsunehiro ; Hayes, C Nelson ; Imamura, Michio ; Aikata, Hiroshi ; Takahashi, Hirokazu ; Torimura, Takuji ; Chayama, Kazuaki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4086-3587307ee9cc2a7aaa7b0a8615e6649a051568cbb24782bb6e58107dcf3537b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Blood glucose</topic><topic>Blood tests</topic><topic>Body mass index</topic><topic>Chromium</topic><topic>Chronic Disease</topic><topic>Continuous glucose monitoring system (CGMS)</topic><topic>Glucose</topic><topic>Glucose Intolerance - diagnosis</topic><topic>Glucose Intolerance - epidemiology</topic><topic>Glucose monitoring</topic><topic>Glucose tolerance</topic><topic>Glycated Hemoglobin A - analysis</topic><topic>HbA1c</topic><topic>Hemoglobin</topic><topic>Humans</topic><topic>Hyperglycemia</topic><topic>Hypoglycemia</topic><topic>Insulin</topic><topic>Insulin resistance</topic><topic>Intolerance</topic><topic>Liver cirrhosis</topic><topic>Liver cirrhosis (LC)</topic><topic>Liver diseases</topic><topic>Liver Diseases - blood</topic><topic>Monitoring systems</topic><topic>Monitoring, Physiologic</topic><topic>Multiple regression analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ogawa, Yutaro</creatorcontrib><creatorcontrib>Nakahara, Takashi</creatorcontrib><creatorcontrib>Ono, Masafumi</creatorcontrib><creatorcontrib>Kawaguchi, Takumi</creatorcontrib><creatorcontrib>Isoda, Hiroshi</creatorcontrib><creatorcontrib>Hiramatsu, Akira</creatorcontrib><creatorcontrib>Uchikawa, Shinsuke</creatorcontrib><creatorcontrib>Fujino, Hatsue</creatorcontrib><creatorcontrib>Murakami, Eisuke</creatorcontrib><creatorcontrib>Kawaoka, Tomokazu</creatorcontrib><creatorcontrib>Yamauchi, Masami</creatorcontrib><creatorcontrib>Tsuge, Masataka</creatorcontrib><creatorcontrib>Munekage, Kensuke</creatorcontrib><creatorcontrib>Ochi, Tsunehiro</creatorcontrib><creatorcontrib>Hayes, C Nelson</creatorcontrib><creatorcontrib>Imamura, Michio</creatorcontrib><creatorcontrib>Aikata, Hiroshi</creatorcontrib><creatorcontrib>Takahashi, Hirokazu</creatorcontrib><creatorcontrib>Torimura, Takuji</creatorcontrib><creatorcontrib>Chayama, Kazuaki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of gastroenterology and hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ogawa, Yutaro</au><au>Nakahara, Takashi</au><au>Ono, Masafumi</au><au>Kawaguchi, Takumi</au><au>Isoda, Hiroshi</au><au>Hiramatsu, Akira</au><au>Uchikawa, Shinsuke</au><au>Fujino, Hatsue</au><au>Murakami, Eisuke</au><au>Kawaoka, Tomokazu</au><au>Yamauchi, Masami</au><au>Tsuge, Masataka</au><au>Munekage, Kensuke</au><au>Ochi, Tsunehiro</au><au>Hayes, C Nelson</au><au>Imamura, Michio</au><au>Aikata, Hiroshi</au><au>Takahashi, Hirokazu</au><au>Torimura, Takuji</au><au>Chayama, Kazuaki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Underestimation of impaired glucose tolerance and usefulness of a continuous glucose monitoring system in chronic liver disease</atitle><jtitle>Journal of gastroenterology and hepatology</jtitle><addtitle>J Gastroenterol Hepatol</addtitle><date>2022-03</date><risdate>2022</risdate><volume>37</volume><issue>3</issue><spage>592</spage><epage>599</epage><pages>592-599</pages><issn>0815-9319</issn><eissn>1440-1746</eissn><abstract>Background and Aim The prevalence of glucose intolerance in chronic liver disease patients is high, but glucose intolerance may be overlooked in a single blood test. The purpose of this study is to evaluate blood glucose variability in patients with chronic liver disease by a continuous glucose monitoring system (CGMS) and to examine the discrepancy between hemoglobin A1c (HbA1c) levels estimated from average blood glucose levels and HbA1c. Methods This study included 335 patients with chronic liver disease associated with glucose intolerance. A fasting blood test and 72‐h CGMS were performed. The estimated HbA1c was calculated from the average blood glucose level, and the correlation between hepatic functional reserve and blood glucose‐related parameters was analyzed. From the obtained data, we created a new formula to calculate HbA1c without using CGMS. Results As hepatic functional reserve decreased, average blood glucose and insulin resistance increased while HbA1c decreased (P &lt; 0.0001). The discrepancy between the estimated HbA1c calculated from the mean blood glucose level and the serum HbA1c (ΔHbA1c) increased as the liver reserve decreased. Using multiple regression analysis, a formula based on fasting blood glucose, HbA1c, body mass index, albumin, and liver function was constructed, and its validity was demonstrated in a study using a different control group. Conclusions Hemoglobin A1c may be underestimated because of decreased hepatic functional reserve. CGMS was useful in assessing accurate glycemic control of blood glucose and in detecting postprandial hyperglycemia and nocturnal hypoglycemia. Patients with chronic hepatic impairment should be corrected for hepatic functional reserve before glycemic control.</abstract><cop>Australia</cop><pub>Wiley Subscription Services, Inc</pub><pmid>34928509</pmid><doi>10.1111/jgh.15766</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-7762-4629</orcidid><orcidid>https://orcid.org/0000-0002-2374-2889</orcidid><orcidid>https://orcid.org/0000-0002-1538-4946</orcidid><orcidid>https://orcid.org/0000-0002-5530-5341</orcidid><orcidid>https://orcid.org/0000-0002-7064-4325</orcidid><orcidid>https://orcid.org/0000-0003-0357-2795</orcidid><orcidid>https://orcid.org/0000-0002-0745-991X</orcidid><orcidid>https://orcid.org/0000-0002-8549-6492</orcidid><orcidid>https://orcid.org/0000-0002-3475-5802</orcidid></addata></record>
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subjects Blood glucose
Blood tests
Body mass index
Chromium
Chronic Disease
Continuous glucose monitoring system (CGMS)
Glucose
Glucose Intolerance - diagnosis
Glucose Intolerance - epidemiology
Glucose monitoring
Glucose tolerance
Glycated Hemoglobin A - analysis
HbA1c
Hemoglobin
Humans
Hyperglycemia
Hypoglycemia
Insulin
Insulin resistance
Intolerance
Liver cirrhosis
Liver cirrhosis (LC)
Liver diseases
Liver Diseases - blood
Monitoring systems
Monitoring, Physiologic
Multiple regression analysis
title Underestimation of impaired glucose tolerance and usefulness of a continuous glucose monitoring system in chronic liver disease
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