Roles of alcohol drinking pattern in fatty liver in Japanese women
Purpose Several studies have reported an inverse association between moderate alcohol consumption and prevalence of fatty liver (FL) in men. We aimed to clarify this association in women. Methods We collected health checkup data from 4,921 Japanese women without concurrent liver disease (mean age 46...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Moriya, Akio [verfasserIn] Iwasaki, Yoshiaki [verfasserIn] Ohguchi, Souhei [verfasserIn] Kayashima, Eizo [verfasserIn] Mitsumune, Tadahiko [verfasserIn] Ikeda, Fusao [verfasserIn] Ando, Masaharu [verfasserIn] Yamamoto, Kazuhide [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2013 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Hepatology international - New York, NY : Springer, 2007, 7(2013), 3 vom: Juli, Seite 859-868 |
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| Übergeordnetes Werk: |
volume:7 ; year:2013 ; number:3 ; month:07 ; pages:859-868 |
| Links: |
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| DOI / URN: |
10.1007/s12072-013-9449-9 |
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| Katalog-ID: |
SPR024206946 |
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| 100 | 1 | |a Moriya, Akio |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Roles of alcohol drinking pattern in fatty liver in Japanese women |
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| 520 | |a Purpose Several studies have reported an inverse association between moderate alcohol consumption and prevalence of fatty liver (FL) in men. We aimed to clarify this association in women. Methods We collected health checkup data from 4,921 Japanese women without concurrent liver disease (mean age 46.4 years) and performed a cross-sectional study to evaluate the influence of alcohol drinking patterns (frequency and amount) on the prevalence of FL as assessed by ultrasonography. Results Alcohol consumption was reported in 30.8 % of participants, and FL was observed in 13.8 % (15.5 % nondrinkers, 10.1 % drinkers). Alcohol consumption was inversely associated with FL prevalence [adjusted odds ratio (AOR) 0.79, 95 % confidence interval (CI) 0.63–0.98]. In analyses stratified by drinking frequency and/or amount of alcohol consumed, the risk of FL decreased for the following categories: 0.1–19.9 g/drinking day (AOR 0.61, 95 % CI 0.44–0.83) and 0.1–69.9 g/week (AOR 0.74, 95 % CI 0.55–0.98). The amount of alcohol consumed directly correlated with the prevalence of FL in daily drinkers (p < 0.05), whereas there was no correlation between the frequency of alcohol consumption and FL prevalence. Alanine aminotransferase levels were significantly lower for the following categories: 0.1–19.9 g/drinking day for 1–3 days a week (p = 0.016) and 0.1–69.9 g within 1–3 drinking days a week (p = 0.004). Conclusions Minimal alcohol consumption appears to have protective effects against nonalcoholic FL disease in women, although an increase in the amount of alcohol consumed appears to nullify the protective effect. | ||
| 650 | 4 | |a Nonalcoholic fatty liver disease |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Metabolic syndrome |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Alcohol consumption |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Drinking frequency |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Ultrasonography |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Iwasaki, Yoshiaki |e verfasserin |4 aut | |
| 700 | 1 | |a Ohguchi, Souhei |e verfasserin |4 aut | |
| 700 | 1 | |a Kayashima, Eizo |e verfasserin |4 aut | |
| 700 | 1 | |a Mitsumune, Tadahiko |e verfasserin |4 aut | |
| 700 | 1 | |a Ikeda, Fusao |e verfasserin |4 aut | |
| 700 | 1 | |a Ando, Masaharu |e verfasserin |4 aut | |
| 700 | 1 | |a Yamamoto, Kazuhide |e verfasserin |4 aut | |
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10.1007/s12072-013-9449-9 doi (DE-627)SPR024206946 (SPR)s12072-013-9449-9-e DE-627 ger DE-627 rakwb eng 610 ASE 44.87 bkl Moriya, Akio verfasserin aut Roles of alcohol drinking pattern in fatty liver in Japanese women 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Purpose Several studies have reported an inverse association between moderate alcohol consumption and prevalence of fatty liver (FL) in men. We aimed to clarify this association in women. Methods We collected health checkup data from 4,921 Japanese women without concurrent liver disease (mean age 46.4 years) and performed a cross-sectional study to evaluate the influence of alcohol drinking patterns (frequency and amount) on the prevalence of FL as assessed by ultrasonography. Results Alcohol consumption was reported in 30.8 % of participants, and FL was observed in 13.8 % (15.5 % nondrinkers, 10.1 % drinkers). Alcohol consumption was inversely associated with FL prevalence [adjusted odds ratio (AOR) 0.79, 95 % confidence interval (CI) 0.63–0.98]. In analyses stratified by drinking frequency and/or amount of alcohol consumed, the risk of FL decreased for the following categories: 0.1–19.9 g/drinking day (AOR 0.61, 95 % CI 0.44–0.83) and 0.1–69.9 g/week (AOR 0.74, 95 % CI 0.55–0.98). The amount of alcohol consumed directly correlated with the prevalence of FL in daily drinkers (p < 0.05), whereas there was no correlation between the frequency of alcohol consumption and FL prevalence. Alanine aminotransferase levels were significantly lower for the following categories: 0.1–19.9 g/drinking day for 1–3 days a week (p = 0.016) and 0.1–69.9 g within 1–3 drinking days a week (p = 0.004). Conclusions Minimal alcohol consumption appears to have protective effects against nonalcoholic FL disease in women, although an increase in the amount of alcohol consumed appears to nullify the protective effect. Nonalcoholic fatty liver disease (dpeaa)DE-He213 Metabolic syndrome (dpeaa)DE-He213 Alcohol consumption (dpeaa)DE-He213 Drinking frequency (dpeaa)DE-He213 Ultrasonography (dpeaa)DE-He213 Iwasaki, Yoshiaki verfasserin aut Ohguchi, Souhei verfasserin aut Kayashima, Eizo verfasserin aut Mitsumune, Tadahiko verfasserin aut Ikeda, Fusao verfasserin aut Ando, Masaharu verfasserin aut Yamamoto, Kazuhide verfasserin aut Enthalten in Hepatology international New York, NY : Springer, 2007 7(2013), 3 vom: Juli, Seite 859-868 (DE-627)524620733 (DE-600)2270316-0 1936-0541 nnns volume:7 year:2013 number:3 month:07 pages:859-868 https://dx.doi.org/10.1007/s12072-013-9449-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.87 ASE AR 7 2013 3 07 859-868 |
| spelling |
10.1007/s12072-013-9449-9 doi (DE-627)SPR024206946 (SPR)s12072-013-9449-9-e DE-627 ger DE-627 rakwb eng 610 ASE 44.87 bkl Moriya, Akio verfasserin aut Roles of alcohol drinking pattern in fatty liver in Japanese women 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Purpose Several studies have reported an inverse association between moderate alcohol consumption and prevalence of fatty liver (FL) in men. We aimed to clarify this association in women. Methods We collected health checkup data from 4,921 Japanese women without concurrent liver disease (mean age 46.4 years) and performed a cross-sectional study to evaluate the influence of alcohol drinking patterns (frequency and amount) on the prevalence of FL as assessed by ultrasonography. Results Alcohol consumption was reported in 30.8 % of participants, and FL was observed in 13.8 % (15.5 % nondrinkers, 10.1 % drinkers). Alcohol consumption was inversely associated with FL prevalence [adjusted odds ratio (AOR) 0.79, 95 % confidence interval (CI) 0.63–0.98]. In analyses stratified by drinking frequency and/or amount of alcohol consumed, the risk of FL decreased for the following categories: 0.1–19.9 g/drinking day (AOR 0.61, 95 % CI 0.44–0.83) and 0.1–69.9 g/week (AOR 0.74, 95 % CI 0.55–0.98). The amount of alcohol consumed directly correlated with the prevalence of FL in daily drinkers (p < 0.05), whereas there was no correlation between the frequency of alcohol consumption and FL prevalence. Alanine aminotransferase levels were significantly lower for the following categories: 0.1–19.9 g/drinking day for 1–3 days a week (p = 0.016) and 0.1–69.9 g within 1–3 drinking days a week (p = 0.004). Conclusions Minimal alcohol consumption appears to have protective effects against nonalcoholic FL disease in women, although an increase in the amount of alcohol consumed appears to nullify the protective effect. Nonalcoholic fatty liver disease (dpeaa)DE-He213 Metabolic syndrome (dpeaa)DE-He213 Alcohol consumption (dpeaa)DE-He213 Drinking frequency (dpeaa)DE-He213 Ultrasonography (dpeaa)DE-He213 Iwasaki, Yoshiaki verfasserin aut Ohguchi, Souhei verfasserin aut Kayashima, Eizo verfasserin aut Mitsumune, Tadahiko verfasserin aut Ikeda, Fusao verfasserin aut Ando, Masaharu verfasserin aut Yamamoto, Kazuhide verfasserin aut Enthalten in Hepatology international New York, NY : Springer, 2007 7(2013), 3 vom: Juli, Seite 859-868 (DE-627)524620733 (DE-600)2270316-0 1936-0541 nnns volume:7 year:2013 number:3 month:07 pages:859-868 https://dx.doi.org/10.1007/s12072-013-9449-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.87 ASE AR 7 2013 3 07 859-868 |
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10.1007/s12072-013-9449-9 doi (DE-627)SPR024206946 (SPR)s12072-013-9449-9-e DE-627 ger DE-627 rakwb eng 610 ASE 44.87 bkl Moriya, Akio verfasserin aut Roles of alcohol drinking pattern in fatty liver in Japanese women 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Purpose Several studies have reported an inverse association between moderate alcohol consumption and prevalence of fatty liver (FL) in men. We aimed to clarify this association in women. Methods We collected health checkup data from 4,921 Japanese women without concurrent liver disease (mean age 46.4 years) and performed a cross-sectional study to evaluate the influence of alcohol drinking patterns (frequency and amount) on the prevalence of FL as assessed by ultrasonography. Results Alcohol consumption was reported in 30.8 % of participants, and FL was observed in 13.8 % (15.5 % nondrinkers, 10.1 % drinkers). Alcohol consumption was inversely associated with FL prevalence [adjusted odds ratio (AOR) 0.79, 95 % confidence interval (CI) 0.63–0.98]. In analyses stratified by drinking frequency and/or amount of alcohol consumed, the risk of FL decreased for the following categories: 0.1–19.9 g/drinking day (AOR 0.61, 95 % CI 0.44–0.83) and 0.1–69.9 g/week (AOR 0.74, 95 % CI 0.55–0.98). The amount of alcohol consumed directly correlated with the prevalence of FL in daily drinkers (p < 0.05), whereas there was no correlation between the frequency of alcohol consumption and FL prevalence. Alanine aminotransferase levels were significantly lower for the following categories: 0.1–19.9 g/drinking day for 1–3 days a week (p = 0.016) and 0.1–69.9 g within 1–3 drinking days a week (p = 0.004). Conclusions Minimal alcohol consumption appears to have protective effects against nonalcoholic FL disease in women, although an increase in the amount of alcohol consumed appears to nullify the protective effect. Nonalcoholic fatty liver disease (dpeaa)DE-He213 Metabolic syndrome (dpeaa)DE-He213 Alcohol consumption (dpeaa)DE-He213 Drinking frequency (dpeaa)DE-He213 Ultrasonography (dpeaa)DE-He213 Iwasaki, Yoshiaki verfasserin aut Ohguchi, Souhei verfasserin aut Kayashima, Eizo verfasserin aut Mitsumune, Tadahiko verfasserin aut Ikeda, Fusao verfasserin aut Ando, Masaharu verfasserin aut Yamamoto, Kazuhide verfasserin aut Enthalten in Hepatology international New York, NY : Springer, 2007 7(2013), 3 vom: Juli, Seite 859-868 (DE-627)524620733 (DE-600)2270316-0 1936-0541 nnns volume:7 year:2013 number:3 month:07 pages:859-868 https://dx.doi.org/10.1007/s12072-013-9449-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.87 ASE AR 7 2013 3 07 859-868 |
| allfieldsGer |
10.1007/s12072-013-9449-9 doi (DE-627)SPR024206946 (SPR)s12072-013-9449-9-e DE-627 ger DE-627 rakwb eng 610 ASE 44.87 bkl Moriya, Akio verfasserin aut Roles of alcohol drinking pattern in fatty liver in Japanese women 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Purpose Several studies have reported an inverse association between moderate alcohol consumption and prevalence of fatty liver (FL) in men. We aimed to clarify this association in women. Methods We collected health checkup data from 4,921 Japanese women without concurrent liver disease (mean age 46.4 years) and performed a cross-sectional study to evaluate the influence of alcohol drinking patterns (frequency and amount) on the prevalence of FL as assessed by ultrasonography. Results Alcohol consumption was reported in 30.8 % of participants, and FL was observed in 13.8 % (15.5 % nondrinkers, 10.1 % drinkers). Alcohol consumption was inversely associated with FL prevalence [adjusted odds ratio (AOR) 0.79, 95 % confidence interval (CI) 0.63–0.98]. In analyses stratified by drinking frequency and/or amount of alcohol consumed, the risk of FL decreased for the following categories: 0.1–19.9 g/drinking day (AOR 0.61, 95 % CI 0.44–0.83) and 0.1–69.9 g/week (AOR 0.74, 95 % CI 0.55–0.98). The amount of alcohol consumed directly correlated with the prevalence of FL in daily drinkers (p < 0.05), whereas there was no correlation between the frequency of alcohol consumption and FL prevalence. Alanine aminotransferase levels were significantly lower for the following categories: 0.1–19.9 g/drinking day for 1–3 days a week (p = 0.016) and 0.1–69.9 g within 1–3 drinking days a week (p = 0.004). Conclusions Minimal alcohol consumption appears to have protective effects against nonalcoholic FL disease in women, although an increase in the amount of alcohol consumed appears to nullify the protective effect. Nonalcoholic fatty liver disease (dpeaa)DE-He213 Metabolic syndrome (dpeaa)DE-He213 Alcohol consumption (dpeaa)DE-He213 Drinking frequency (dpeaa)DE-He213 Ultrasonography (dpeaa)DE-He213 Iwasaki, Yoshiaki verfasserin aut Ohguchi, Souhei verfasserin aut Kayashima, Eizo verfasserin aut Mitsumune, Tadahiko verfasserin aut Ikeda, Fusao verfasserin aut Ando, Masaharu verfasserin aut Yamamoto, Kazuhide verfasserin aut Enthalten in Hepatology international New York, NY : Springer, 2007 7(2013), 3 vom: Juli, Seite 859-868 (DE-627)524620733 (DE-600)2270316-0 1936-0541 nnns volume:7 year:2013 number:3 month:07 pages:859-868 https://dx.doi.org/10.1007/s12072-013-9449-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.87 ASE AR 7 2013 3 07 859-868 |
| allfieldsSound |
10.1007/s12072-013-9449-9 doi (DE-627)SPR024206946 (SPR)s12072-013-9449-9-e DE-627 ger DE-627 rakwb eng 610 ASE 44.87 bkl Moriya, Akio verfasserin aut Roles of alcohol drinking pattern in fatty liver in Japanese women 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Purpose Several studies have reported an inverse association between moderate alcohol consumption and prevalence of fatty liver (FL) in men. We aimed to clarify this association in women. Methods We collected health checkup data from 4,921 Japanese women without concurrent liver disease (mean age 46.4 years) and performed a cross-sectional study to evaluate the influence of alcohol drinking patterns (frequency and amount) on the prevalence of FL as assessed by ultrasonography. Results Alcohol consumption was reported in 30.8 % of participants, and FL was observed in 13.8 % (15.5 % nondrinkers, 10.1 % drinkers). Alcohol consumption was inversely associated with FL prevalence [adjusted odds ratio (AOR) 0.79, 95 % confidence interval (CI) 0.63–0.98]. In analyses stratified by drinking frequency and/or amount of alcohol consumed, the risk of FL decreased for the following categories: 0.1–19.9 g/drinking day (AOR 0.61, 95 % CI 0.44–0.83) and 0.1–69.9 g/week (AOR 0.74, 95 % CI 0.55–0.98). The amount of alcohol consumed directly correlated with the prevalence of FL in daily drinkers (p < 0.05), whereas there was no correlation between the frequency of alcohol consumption and FL prevalence. Alanine aminotransferase levels were significantly lower for the following categories: 0.1–19.9 g/drinking day for 1–3 days a week (p = 0.016) and 0.1–69.9 g within 1–3 drinking days a week (p = 0.004). Conclusions Minimal alcohol consumption appears to have protective effects against nonalcoholic FL disease in women, although an increase in the amount of alcohol consumed appears to nullify the protective effect. Nonalcoholic fatty liver disease (dpeaa)DE-He213 Metabolic syndrome (dpeaa)DE-He213 Alcohol consumption (dpeaa)DE-He213 Drinking frequency (dpeaa)DE-He213 Ultrasonography (dpeaa)DE-He213 Iwasaki, Yoshiaki verfasserin aut Ohguchi, Souhei verfasserin aut Kayashima, Eizo verfasserin aut Mitsumune, Tadahiko verfasserin aut Ikeda, Fusao verfasserin aut Ando, Masaharu verfasserin aut Yamamoto, Kazuhide verfasserin aut Enthalten in Hepatology international New York, NY : Springer, 2007 7(2013), 3 vom: Juli, Seite 859-868 (DE-627)524620733 (DE-600)2270316-0 1936-0541 nnns volume:7 year:2013 number:3 month:07 pages:859-868 https://dx.doi.org/10.1007/s12072-013-9449-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.87 ASE AR 7 2013 3 07 859-868 |
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English |
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Enthalten in Hepatology international 7(2013), 3 vom: Juli, Seite 859-868 volume:7 year:2013 number:3 month:07 pages:859-868 |
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Enthalten in Hepatology international 7(2013), 3 vom: Juli, Seite 859-868 volume:7 year:2013 number:3 month:07 pages:859-868 |
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Nonalcoholic fatty liver disease Metabolic syndrome Alcohol consumption Drinking frequency Ultrasonography |
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Hepatology international |
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Moriya, Akio @@aut@@ Iwasaki, Yoshiaki @@aut@@ Ohguchi, Souhei @@aut@@ Kayashima, Eizo @@aut@@ Mitsumune, Tadahiko @@aut@@ Ikeda, Fusao @@aut@@ Ando, Masaharu @@aut@@ Yamamoto, Kazuhide @@aut@@ |
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2013-07-01T00:00:00Z |
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We aimed to clarify this association in women. Methods We collected health checkup data from 4,921 Japanese women without concurrent liver disease (mean age 46.4 years) and performed a cross-sectional study to evaluate the influence of alcohol drinking patterns (frequency and amount) on the prevalence of FL as assessed by ultrasonography. Results Alcohol consumption was reported in 30.8 % of participants, and FL was observed in 13.8 % (15.5 % nondrinkers, 10.1 % drinkers). Alcohol consumption was inversely associated with FL prevalence [adjusted odds ratio (AOR) 0.79, 95 % confidence interval (CI) 0.63–0.98]. In analyses stratified by drinking frequency and/or amount of alcohol consumed, the risk of FL decreased for the following categories: 0.1–19.9 g/drinking day (AOR 0.61, 95 % CI 0.44–0.83) and 0.1–69.9 g/week (AOR 0.74, 95 % CI 0.55–0.98). The amount of alcohol consumed directly correlated with the prevalence of FL in daily drinkers (p < 0.05), whereas there was no correlation between the frequency of alcohol consumption and FL prevalence. Alanine aminotransferase levels were significantly lower for the following categories: 0.1–19.9 g/drinking day for 1–3 days a week (p = 0.016) and 0.1–69.9 g within 1–3 drinking days a week (p = 0.004). 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Moriya, Akio |
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Moriya, Akio ddc 610 bkl 44.87 misc Nonalcoholic fatty liver disease misc Metabolic syndrome misc Alcohol consumption misc Drinking frequency misc Ultrasonography Roles of alcohol drinking pattern in fatty liver in Japanese women |
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610 ASE 44.87 bkl Roles of alcohol drinking pattern in fatty liver in Japanese women Nonalcoholic fatty liver disease (dpeaa)DE-He213 Metabolic syndrome (dpeaa)DE-He213 Alcohol consumption (dpeaa)DE-He213 Drinking frequency (dpeaa)DE-He213 Ultrasonography (dpeaa)DE-He213 |
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roles of alcohol drinking pattern in fatty liver in japanese women |
| title_auth |
Roles of alcohol drinking pattern in fatty liver in Japanese women |
| abstract |
Purpose Several studies have reported an inverse association between moderate alcohol consumption and prevalence of fatty liver (FL) in men. We aimed to clarify this association in women. Methods We collected health checkup data from 4,921 Japanese women without concurrent liver disease (mean age 46.4 years) and performed a cross-sectional study to evaluate the influence of alcohol drinking patterns (frequency and amount) on the prevalence of FL as assessed by ultrasonography. Results Alcohol consumption was reported in 30.8 % of participants, and FL was observed in 13.8 % (15.5 % nondrinkers, 10.1 % drinkers). Alcohol consumption was inversely associated with FL prevalence [adjusted odds ratio (AOR) 0.79, 95 % confidence interval (CI) 0.63–0.98]. In analyses stratified by drinking frequency and/or amount of alcohol consumed, the risk of FL decreased for the following categories: 0.1–19.9 g/drinking day (AOR 0.61, 95 % CI 0.44–0.83) and 0.1–69.9 g/week (AOR 0.74, 95 % CI 0.55–0.98). The amount of alcohol consumed directly correlated with the prevalence of FL in daily drinkers (p < 0.05), whereas there was no correlation between the frequency of alcohol consumption and FL prevalence. Alanine aminotransferase levels were significantly lower for the following categories: 0.1–19.9 g/drinking day for 1–3 days a week (p = 0.016) and 0.1–69.9 g within 1–3 drinking days a week (p = 0.004). Conclusions Minimal alcohol consumption appears to have protective effects against nonalcoholic FL disease in women, although an increase in the amount of alcohol consumed appears to nullify the protective effect. |
| abstractGer |
Purpose Several studies have reported an inverse association between moderate alcohol consumption and prevalence of fatty liver (FL) in men. We aimed to clarify this association in women. Methods We collected health checkup data from 4,921 Japanese women without concurrent liver disease (mean age 46.4 years) and performed a cross-sectional study to evaluate the influence of alcohol drinking patterns (frequency and amount) on the prevalence of FL as assessed by ultrasonography. Results Alcohol consumption was reported in 30.8 % of participants, and FL was observed in 13.8 % (15.5 % nondrinkers, 10.1 % drinkers). Alcohol consumption was inversely associated with FL prevalence [adjusted odds ratio (AOR) 0.79, 95 % confidence interval (CI) 0.63–0.98]. In analyses stratified by drinking frequency and/or amount of alcohol consumed, the risk of FL decreased for the following categories: 0.1–19.9 g/drinking day (AOR 0.61, 95 % CI 0.44–0.83) and 0.1–69.9 g/week (AOR 0.74, 95 % CI 0.55–0.98). The amount of alcohol consumed directly correlated with the prevalence of FL in daily drinkers (p < 0.05), whereas there was no correlation between the frequency of alcohol consumption and FL prevalence. Alanine aminotransferase levels were significantly lower for the following categories: 0.1–19.9 g/drinking day for 1–3 days a week (p = 0.016) and 0.1–69.9 g within 1–3 drinking days a week (p = 0.004). Conclusions Minimal alcohol consumption appears to have protective effects against nonalcoholic FL disease in women, although an increase in the amount of alcohol consumed appears to nullify the protective effect. |
| abstract_unstemmed |
Purpose Several studies have reported an inverse association between moderate alcohol consumption and prevalence of fatty liver (FL) in men. We aimed to clarify this association in women. Methods We collected health checkup data from 4,921 Japanese women without concurrent liver disease (mean age 46.4 years) and performed a cross-sectional study to evaluate the influence of alcohol drinking patterns (frequency and amount) on the prevalence of FL as assessed by ultrasonography. Results Alcohol consumption was reported in 30.8 % of participants, and FL was observed in 13.8 % (15.5 % nondrinkers, 10.1 % drinkers). Alcohol consumption was inversely associated with FL prevalence [adjusted odds ratio (AOR) 0.79, 95 % confidence interval (CI) 0.63–0.98]. In analyses stratified by drinking frequency and/or amount of alcohol consumed, the risk of FL decreased for the following categories: 0.1–19.9 g/drinking day (AOR 0.61, 95 % CI 0.44–0.83) and 0.1–69.9 g/week (AOR 0.74, 95 % CI 0.55–0.98). The amount of alcohol consumed directly correlated with the prevalence of FL in daily drinkers (p < 0.05), whereas there was no correlation between the frequency of alcohol consumption and FL prevalence. Alanine aminotransferase levels were significantly lower for the following categories: 0.1–19.9 g/drinking day for 1–3 days a week (p = 0.016) and 0.1–69.9 g within 1–3 drinking days a week (p = 0.004). Conclusions Minimal alcohol consumption appears to have protective effects against nonalcoholic FL disease in women, although an increase in the amount of alcohol consumed appears to nullify the protective effect. |
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Roles of alcohol drinking pattern in fatty liver in Japanese women |
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Iwasaki, Yoshiaki Ohguchi, Souhei Kayashima, Eizo Mitsumune, Tadahiko Ikeda, Fusao Ando, Masaharu Yamamoto, Kazuhide |
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| score |
7.399974 |