- Research article
- Open Access
Discrimination of individuals in a general population at high-risk for alcoholic and non-alcoholic fatty liver disease based on liver stiffness: a cross section study
BMC Gastroenterology volume 11, Article number: 70 (2011)
Factors associated with liver stiffness (LS) are unknown and normal reference values for LS have not been established. Individuals at high risk for alcoholic (ALD) and non-alcoholic fatty (NAFLD) liver disease need to be non-invasively discriminated during routine health checks. Factors related to LS measured using a FibroScan and normal reference values for LS are presented in this report.
We measured LS using a FibroScan in 416 consecutive individuals who presented for routine medical checks. We also investigated the relationship between LS and age, body mass index (BMI), liver function (LF), alcohol consumption, and fatty liver determined by ultrasonography. We identified individuals at high-risk for ALD and NAFLD as having a higher LS value than the normal upper limit detected in 171 healthy controls.
The LS value for all individuals was 4.7 +/- 1.5 kPa (mean +/- SD) and LS significantly and positively correlated with BMI and LF test results. The LS was significantly higher among individuals with, than without fatty liver. Liver stiffness in the 171 healthy controls was 4.3 +/- 0.81 kPa and the upper limit of LS in the normal controls was 5.9 kPa. We found that 60 (14.3%) of 416 study participants had abnormal LS. The proportion of individuals whose LS values exceeded the normal upper limit was over five-fold higher among those with, than without fatty liver accompanied by abnormal LF test results.
Liver stiffness could be used to non-invasively monitor the progression of chronic liver diseases and to discriminate individuals at high risk for ALD and NAFLD during routine health assessments.
A large body of evidence supports the importance of liver biopsies for understanding the progression of chronic liver disease . Although liver biopsy is the gold standard for diagnosing chronic liver disease and for determining the extent of liver fibrosis, adverse effects and sampling errors are associated with the procedure [2–7], because a standard liver biopsy samples only about 1/50,000 of the liver . In addition, the role of the liver biopsy in nonalcoholic fatty liver disease (NAFLD) is controversial. Arguments against routine liver biopsy include the generally benign course of NAFLD, the absence of established effective therapies even when findings indicate a need for treatment, and the risks associated with liver biopsy .
To distinguish nonalcoholic steatohepatitis (NASH) from NAFLD in routine practice is difficult. Efforts have been made to diagnose NASH using various imaging studies and blood tests, but the outcome has remained inadequate .
The FibroScan (Echo Sens, Paris, France) is a new transient elastometer that can noninvasively measure LS [11, 12]. Correlations between LS and fibrosis have been reported [13, 14] and monitoring LS might provide a method for observing and judging the progression of chronic liver diseases, including fatty liver disease .
Various clinical factors other than fibrosis itself, including necroinflammation of the liver, cholestasis and congestive heart failure can affect LS regardless of the severity of fibrosis [13, 14]. However, factors influencing LS in apparently healthy subjects other than liver fibrosis have not been sufficiently clarified [16–19]. Almost all European studies have focused on patients with chronic liver disease. Although a few studies have evaluated healthy individuals from the viewpoint of defining normal reference values for LS [16, 17], some of those included might have had subclinical liver disease. Therefore, normal reference values for of LS still need to be established based on data from healthy persons who are considered not to have liver disease at any stage.
The present study explores factors related to LS, establishes normal reference values for LS in healthy individuals, and determines whether LS can help to identify individuals at high-risk for ALD and NAFLD.
This study enrolled 423 consecutive Japanese individuals between the ages of 20 and 68 years (250 males; hepatitis B surface antigen negative; hepatitis C virus antibody negative), who presented for annual medical checkups at our health examination centre between July 2004 and April 2006. We excluded individuals with a history of any liver or cardiac diseases (especially congestive heart failure) and those who were under treatment for such conditions. We also excluded those with platelet counts < 150,000/μL. A medical history was obtained from each of the 423 persons, who then underwent a physical examination, a chest X-ray, electrocardiography and standard laboratory tests including FBS and HbA1c. Seven were excluded because LS could not be measured due to extensive intercostal subcutaneous tissue depth. Finally, 416 individual (250 males) were enrolled in this study. All participants provided written informed consent to participate in this study, which proceeded according to the Declaration of Helsinki and under the approval of our institutional review board.
Abdominal ultrasonography and liver stiffness measured by transient elastography
We used ultrasonography to diagnose fatty liver based on hepatorenal contrast visualization, increased ultrasonographic signals in the liver parenchyma and decreased signals from deep areas of the liver. We also confirmed the absence of space-occupying lesions in the liver. Stiffness was measured in the right lobe of the liver accessed using a FibroScan through the intercostal spaces of participants placed in the dorsal decubitus position with the right arm in maximal abduction. Technical and procedural details have been described [13, 20]. In brief, the FibroScan is equipped with a probe that includes an ultrasonic transducer. The tip of the transducer is covered with gel and placed on a specific location. A low-frequency, mild amplitude vibration is transmitted to the liver from the tip of the transducer. This vibration induces an elastic shear wave, of which the propagation and velocity are measured by simultaneous ultrasonography and expressed in kilopascals (kPa). These properties are directly related to liver tissue stiffness. Higher values indicate increased liver stiffness. Up to 10 measurements were obtained from each participant, and LS is represented as median values. Only procedures with at least 10 valid measurements, a success rate of at least 60% and an IQR to median value ratio of < 30% were considered reliable . The success rate and IQR in this study were 94% and 17%, respectively. The FibroScan measures LS in a volume that approximates a 4-cm long cylinder with a diameter of 1 cm located between 2.5 and 6.5 cm below the skin surface. This volume is about 100-fold larger than a standard liver biopsy specimen, and thus might be more representative of the entire hepatic parenchyma. Individuals (N = 7) with intercostal subcutaneous tissues ≥ 25 mm [11–13] were excluded from the study because liver stiffness could not be measured under such conditions using the FibroScan.
Measurement of physical findings and liver function tests
Height and weight were measured and BMI was calculated. To further assess the impact of body weight, we assigned the 416 participants into groups based on BMI < 23, 23 to ≤ 25, and > 25. The thickness of the intercostal subcutaneous tissues was measured only to confirm whether LS could be measured. Daily amounts and duration of alcohol consumption were evaluated using a formal, written questionnaire and total amounts of consumed alcohol were calculated as quantities of pure alcohol. Since alcohol consumption of ≤ 20 g of per day is prerequisite for a definition of NASH, we assigned the 416 participants into groups based on daily alcohol consumption of ≤ 20 and > 20 g/day (non-/occasional and habitual consumption, respectively) [20, 22]. Liver function (LF) was tested in terms of serum levels of aspartate 2-oxoglutarate aminotransferase (AST), alanine aminotransferase (ALT) and γ-glutamyltranspeptidase (γ-GTP). The normal upper limits of AST, ALT and γ-GTP at our health centre are 35, 35 and 55 U/L, respectively. We defined normal LF tests results as each of AST, ALT and γ-GTP being within normal limits.
Influence of liver dysfunction and fatty liver on LS
The participants were separated based on LF tests results and the presence or absence of fatty liver into Group 1 (N = 260), normal LF and no fatty liver; Group 2 (N = 32), abnormal LF and no fatty liver; Group 3 (N = 60), normal LF and fatty liver; Group 4 (N = 59), abnormal LF and fatty liver.
Relationship between LS and platelet counts or platelet ratio index
We counted platelets and calculated the AST to platelet ratio index (APRI) to determine the relationship between LS and apparent liver fibrosis in all participants .
Determination of normal reference values for liver stiffness
We selected healthy control candidates based on the following criteria: BMI < 23 kg/m2, normal LF, no findings of fatty liver by ultrasonography and daily alcohol consumption ≤ 20 g/day. We defined being overweight and obesity based on the World Health Organization (WHO) criteria for the Western Pacific Region as BMI ≥ 23 and ≥ 25 kg/m2, respectively [22, 24]. None of our healthy control candidates fulfilled the criteria for metabolic syndrome proposed by International Diabetes Federation . Furthermore, to establish normal reference values based on stricter criteria, candidates had to meet any one of the following conditions: triglycerides, < 150 mg/dL; HDL cholesterol, ≥ 40 mg/dL in men and ≥ 50 mg/dL in women; blood pressure, < 130/85 mmHg and fasting plasma glucose, < 100 mg/dL. We excluded six candidates because of high blood pressure. We finally selected 165 (77 males) of the 416 participants who met the criteria described above as normal controls (Figure 1)
Continuous variables are expressed as means ± SD. The relationship between LS and each variable was assessed using Pearson's correlation coefficient and LS was compared between two groups using the unpaired Student's t-test. Differences among more than three groups were analyzed using the analysis of variance (ANOVA) when variables were normally distributed, followed by multiple comparisons. Categorical data were compared using the χ2 test and the Cochran-Armitage test for trends. Both univariate and multivariate analyses were performed using logistic regression models. P < 0.05 was considered to represent a statistically significant difference. Data were statistically analysed using JMP 9.01 software (SAS Institute Inc., Cary, NC).
Table 1 shows the background characteristics of all participants and controls. The value for LS in all (N = 416) participants was 4.73 ± 1.54 kPa (range, 2.3-18.6 kPa) and that in healthy controls (N = 165) was 4.30 ± 0.81 kPa (range, 2.7-7.4 kPa) with a normal upper limit of 5.9 kPa (mean + 2SD). Liver stiffness tended to increase with age in all participants, although the difference did not reach statistical significance (p = 0.11).
Liver stiffness values were significantly higher in males than in females among all participants (4.88 ± 1.77 vs. 4.52 ± 1.11 kPa, respectively, p = 0.02), but did not significantly differ between healthy control males and females (4.41 ± 0.79 vs. 4.20 ± 0.83 kPa, respectively, p = 0.10).
Liver stiffness significantly correlated with BMI in all participants (Table 2). Mean LS based on BMI (ANOVA p < 0.0001; Figure 2) and the proportion of those with LS beyond the normal upper limit (x 2 = 14.31, p = 0.0008) also significantly differed among the three groups. The Cochran-Armitage test for trend also showed a linear trend for proportions across these groups (Z = 3.84, p < 0.0001).
Values for LS were significantly higher among individuals with, than without fatty liver. Ratios of those with LS above normal upper limit significantly differed (x 2 = 37.54, p < 0.0001; Figure 3).
Liver stiffness did not correlate with daily or total alcohol consumption (Table 2) and did not significantly differ between those with no or occasional alcohol consumption, and those with habitual consumption. However the ratio of those with LS above the normal upper limit was significantly higher in the group who habitually consumed alcohol (x 2 = 7.15, p = 0.008; Figure 4).
Liver stiffness significantly and positively correlated with levels of AST or ALT, and with APRI but not with γ-GTP (Table 2) or platelet counts in all participants.
We found that 60 (14.3%) of the 416 participants had higher LS. We also found that LS significantly differed between the presence and absence of fatty liver (ANOVA, p < 0.0001) when the participants were assigned to four groups based on the results of LF tests. In addition, LS was the highest in Group 4, and higher in Group 3 than in Group 1 according to multiple comparisons (Figure 5). Nineteen (7.1%), 4 (12.5%), 14 (23.3%) and 23 (39.0%) participants in Groups 1, 2, 3 and 4, respectively, had LS values above the normal upper limit and the proportions significantly differed among the four groups (x 2 = 37.54, p < 0.0001). The Cochran-Armitage test for trend also showed a linear trend in proportions across the four groups (Z = 6.48, p < 0.0001; Figure 6).
Figure 7 shows a comparison of liver stiffness among four groups based on alcohol consumption and fatty liver. All participants were assigned to two groups based on alcohol consumption and then each group was subdivided into two groups based on the presence or absence of fatty liver according to ultrasonography (Groups A, B, C and D). About 7% (6.9% and 7.5%) of all participants had LS above 5.9 kPa among those with NAFLD or ALD regardless of fatty liver. We could not exclude subclinical fatty changes that were undetectable by ultrasonography in Groups A and C. We thus speculated that liver stiffness can discriminate hepatic abnormalities more effectively than conventional ultrasonography.
Univariate analysis found that BMI, alcohol consumption, abnormal LF test results, fatty liver and APRI were associated with LS.
We excluded abnormal LF test results and fatty liver as confounding factors in multivariate analysis because these can result from a higher BMI or habitual alcohol consumption. We also excluded APRI because this merely reflected serum levels of AST in this study population. Finally, we included BMI and alcohol consumption in the multivariate analysis model.
Multivariate analysis revealed that BMI (23 - 25 kg/m2: odds ratio (OR), 2.21; 95% confidence interval (CI), 1.06-4.46; p = 0.033; ≥ 25 kg/m2: OR, 3.25; 95% CI, 1.62-6.43; p = 0.001) was the only independent predictor of higher LS (Table 3).
We described factors related to LS and defined normal reference values for liver stiffness among healthy control individuals. We also showed that individuals at high risk for ALD and NAFLD could be discriminated by measuring LS using a FibroScan, which is useful for assessing patients with confirmed chronic liver disease . However, few studies have examined its relevance to a first-line diagnosis of liver disorders and to identifying patients at high risk during routine medical checks.
The present study found no significant statistical differences between healthy control males and females, although all enrolled participants significantly differed. Whether gender should be taken into account when interpreting liver stiffness has been disputed, because several confounders between gender and BMI, metabolic syndrome, and alcohol consumption have not been appropriately adjusted [16, 17, 19].
We investigated which factors are related to LS before determining the normal upper limit of LS. Factors associated with LS in all participants were BMI, the presence of fatty liver, alcohol consumption and serum levels of AST and ALT. These findings suggested that being overweight (including obesity), habitual alcohol consumption and abnormal LF test results are important factors associated with a higher LS. We then selected those who met our criteria for normal controls based on these findings.
One of the major reasons for the higher LS in individuals with a high BMI seemed to be liver steatosis caused by NAFLD or ALD. Mean liver stiffness was higher in individuals with, than without fatty liver, but the distribution of LS widely overlapped between the two groups. We speculated that factors in addition to steatosis would be involved in increased LS. We considered that the mechanisms involved in the increase in the LS in our study population might be related to inflammatory cell invasion, liver cell degeneration and liver fibrosis as well as steatosis, all of which have been pathologically demonstrated in patients with NASH and ALD . Whether or not simple steatosis alone would increase LS remains to be resolved.
The normal upper limit of LS was determined based on patients with a BMI < 23 kg/m2 in this study. However, if the upper limit was based on the WHO global criteria for obesity of BMI ≥ 25 kg/m2, , then LS and the upper limit of LS in controls would be 4.44 ± 1.05 and 6.5 kPa, respectively.
Daily or total alcohol consumption significantly and positively correlated with γ-GTP levels in our study population (data not shown) as described [29, 30]. The absence of correlations between LS and daily or total alcohol consumption can be explained by individual genetic differences in alcohol metabolism and the presence of a higher LS in patients with NAFLD [23, 31]. The ratio of individuals with LS beyond the normal upper limit was significantly higher among those who habitually consumed alcohol than in those who did not consume, or who occasionally consumed alcohol. Therefore, alcohol consumption seems to be an important factor that affects LS. Although a normal upper limit of LS was established for participants who consumed ≤ 20 g of alcohol/day, LS and the upper limits of LS in controls (N = 91 of 165) who did not consume alcohol were 4.15 ± 0.66 and 5.5 kPa, respectively. This normal upper limit of LS was essentially equivalent to that reported by Kim et al. We considered that to determine the effect of consuming a very small amount of alcohol on LS in this population would be almost impossible, so we adopted alcohol consumption criteria of ≤ 20 g/day.
The present study found that LS was related to AST and ALT levels or APRI, which significantly correlates with stage of fibrosis and with a higher correlation coefficient than platelet count or AST levels alone in patients with chronic hepatitis C infection . Because our study population was limited to individuals who presented for annual medical checkups, LS was more closely correlated with AST than with APRI, and did not associate with platelet counts. Liver damage that causes AST/ALT elevation also appeared to influence LS, because LS is higher even in patients with acute viral hepatitis but without liver fibrosis .
Univariate analysis indicated that BMI, alcohol consumption, LF test results and fatty liver status were associated with LS. Among these, the three BMI categories were significantly associated with fatty liver (χ2 = 100.69, p < 0.0001). Alcohol consumption also significantly associated with abnormal LF test results (χ2 = 26.8, p < 0.0001). We assumed that being overweight and habitual alcohol consumption can cause abnormal LF tests results and fatty liver, so BMI and alcohol consumption were included in the multivariate logistic regression model. Finally, BMI was identified, as the only independent predictor of higher LS and LS was significantly higher even in the group with BMI 23 - 25 kg/m2. Although interpreting LS might be subject to ethnic differences, we considered that our BMI criteria were appropriate for inclusion among normal reference values. Cobbold et al. have highlighted some issues regarding LS and BMI .
Table 4 summarizes two published reports and our study. Roulot et al.  examined a large cohort of apparently healthy individuals with no evidence of liver disease and established normal liver stiffness values (5.60 ± 1.30 kPa in males, 5.05 ± 1.49 kPa in females. Although their normal upper limit of liver stiffness were relatively high and almost corresponded to METAVIRE fibrosis stage 2 (LS = 7.2 kPa) [14, 19].
Kim et al.  established a normal liver stiffness value (4.5 ± 0.4 kPa) based on a study of 69 healthy liver and kidney donors who passed screening evaluations for transplantation, whose laboratory findings were normal, and who could be regarded as being healthy and free of liver disease. Our normal upper limits of liver stiffness were nearly equivalent to theirs, which was lower than that of Roulot et al. The study population and criteria for healthy controls shown in Table 4 probably can account for these differences.
Liver disorders are usually screened during routine medical checkups or in clinical practice using LF tests and ultrasonography. Figures 5, 6 and 7 show that LS (in addition to a standard set of LF tests and ultrasonography) can discriminate individuals at high risk for non-alcoholic and alcoholic liver diseases.
While investigations of the pathogenesis of various liver diseases are important, liver biopsies are not always feasible because of adverse effects, and were unobtainable from our population from an ethical standpoint. Nevertheless, our reference values for LS would be useful to select candidates for liver biopsy and thus decrease the rate of unnecessary procedures.
In conclusion, our study uncovered several factors that are associated with LS, and showed that measuring LS is a non-invasive, simple and efficient method of identifying individuals at high risk for ALD and NAFLD. Future studies should investigate pathological factors other than fibrosis that influence LS in clinical populations.
alcoholic liver disease
ratio of aspartate 2-oxoglutarate aminotransferase to platelet ratio index
aspartate 2-oxoglutarate aminotransferase
body mass index
nonalcoholic fatty liver disease
Neuschwander-Tetri BA, Caldwell SH: Nonalcoholic steatohepatitis: summary of an AASLD Single Topic Conference. Hepatology. 2003, 37: 1202-19. 10.1053/jhep.2003.50193.
Ratziu V, Charlotte F, Heurtier A, Gombert S, Giral P, Bruckert E, Grimaidi A, Capron F: Sampling variability of liver biopsy in nonalcoholic fatty liver disease. Gastroenterology. 2005, 128: 1898-906. 10.1053/j.gastro.2005.03.084.
Bedossa P, Dargere D, Paradis V: Sampling variability of liver fibrosis in chronic hepatitis C. Hepatology. 2003, 38: 1449-57.
Maharaj B, Maharaja RJ, Leary WP, Coopan RM, Naran AD, Pirie D: Sampling variability and its influence on the diagnostic yield of percutaneous needle biopsy of the liver. Lancet. 1986, 8: 523-5. 10.1016/S0140-6736(86)90883-4.
Regev A, Berho M, Jeffers LJ, Milikowski C, Molina EG, Pyrsopoulos NT, Feng Z-Z, Reddy KR, Schiff ER: Sampling error and intraobserver variation in liver biopsy in patients with chronic HCV infection. Am J Gastroenterol. 2002, 97: 2614-8. 10.1111/j.1572-0241.2002.06038.x.
Soloway RD, Baggenstoss AH, Schoenfield LJ, Summerskill WHJ: Observer error and sampling variability tested in evaluation of hepatitis and cirrhosis by liver biopsy. Am J Dig Dis. 1971, 16: 1082-6. 10.1007/BF02235164.
Abdi W, Millan JC, Mezey E: Sampling variability on percutaneous liver biopsy. Arch Intern Med. 1979, 139: 667-9. 10.1001/archinte.139.6.667.
Bravo Arturo, Sheth Sunil, Sanjiv C: Liver biopsy. N Engl J Med. 2001, 344: 495-500. 10.1056/NEJM200102153440706.
Bayard M, Holt J, Boroughs E: Nonalcoholic fatty liver disease. Am Fam Physician. 2006, 73: 1961-8.
Saadeh S, Younossi ZM, Remer EM, Gramlich T, Ong JP, Hurley M, Mullen KD, Cooper JN, Sheridan MJ: The utility of radiological imaging in nonalcoholic fatty liver disease. Gastroenterology. 2002, 123: 745-50. 10.1053/gast.2002.35354.
Sandrin L, Tanter M, Gennisson J-L, Catheline S, Fink M: Shear elasticity probe for soft tissues with 1-D transient elastography. IEEE Trans Ultrason Ferroelectr Freq Control. 2002, 49: 436-46. 10.1109/58.996561.
Yeh W-C, Li P-C, Jeng Y-M, Hsu H-C, Kuo P-L, Li M-L, Yang P-M, Lee PH: Elastic modulus measurements of human liver and correlation with pathology. Ultrasound in Med Biol. 2002, 28: 467-74. 10.1016/S0301-5629(02)00489-1.
Ziol M, Handra-Luca A, Kettaneh A, Christidis C, Mal F, Kazemi F, Ledinghrn V, Marcellin P, Dhumeaux D, Trinchet J-C, Beaugrand M: Noninvasive assessment of liver fibrosis by measurement of stiffness in patients with chronic hepatitis C. Hepatology. 2005, 41: 48-54. 10.1002/hep.20506.
Foucher J, Chanteloup E, Vergniol J, Castera L, Bail BL, Adhoute X, Bertet J, Couzigou P, Ledinghen V: Diagnosis of cirrhosis by transient elastography (FibroScan): a prospective study. Gut. 2006, 55: 403-8. 10.1136/gut.2005.069153.
Sandrin L, Fourquet B, Hasquenoph J-M, Yon S, Fournier C, Mal F, Christidis C, Ziol M, Poulet B, Kazemi F, Beaugrand M, Palau R: Transient elastography: A new noninvasive method for assessment of hepatic fibrosis. Ultrasound in Med Biol. 2003, 29: 1705-13. 10.1016/j.ultrasmedbio.2003.07.001.
Roulot D, Czernichow S, Le Clesiau H, Costes J-L, Vergnaud A-C, Beaugrand M: Liver stiffness values in apparently healthy subjects: Influence of gender and metabolic syndrome. Journal of Hepatology. 2008, 48: 606-613. 10.1016/S0168-8278(08)60967-8.
Kim SU, Choi GH, Han WK, Kim BK, Park JK, Kim do Y, Choi JS, Yang SC, Choi EH, Ahn SH, Han KH, Chon CY: What are 'true normal' liver stiffness values using FibroScan?; a prospective study in healthy living liver and kidney donors in South Korea. Liver International. 2010, 268-274. 10.1111/j.1478-3231.2009.02172.x.
Corpechot C, El Naggar A, Poupon R: Gender and liver: Is the liver stiffness weaker in weaker sex?. Hepatology. 2006, 44: 513-514. 10.1002/hep.21306.
Cobbold Jeremy, Taylor-Robinson Simon: Liver stiffness values in healthy subjects: Implications for clinical practice. Journal of Hepatology. 2008, 48: 529-531. 10.1016/j.jhep.2008.01.005.
Kawamoto M, Mizuguchi T, Katsuramaki T, Nagayama M, Oshima H, Kawasaki H, Noboru T, Kimura Y, Hirata K: Assessment of liver fibrosis by a noninvasive method of transient elastography and biochemical markers. World J Gastroenterol. 2006, 12: 4325-30.
Alexandre D, Roxana S, Alina P: Feasibility, accuracy and reproducibility of transient elastography. Medical Ultrasonography. 2009, 11: 31-35.
Ko GTC, Chan JCN, Cockram CS: Prediction of hypertension, diabetes, dyslipidemia or albuminuria using simple anthropometric indexes in Hong Kong Chinese. Int J Obes. 1999, 23: 1136-42. 10.1038/sj.ijo.0801043.
Luczak SE, Elvine-Kreis B, Shea SH: Genetic risk for alcoholism relates to level of response to alcohol in Asian-American men and women. J Stud Alcohol. 2002, 63: 74-82.
Deurenberg-Yap M, Yian TB, Kai CS: Manifestation of cardiovascular risk factors at low levels of body mass index and waist-to-hip ratio in Singaporean Chinese. Asian Pacific J Clin Nutr. 1999, 8: 177-83. 10.1046/j.1440-6047.1999.00091.x.
Alberti KG, Zimmet P, Shaw J: The metabolic syndrome - a new worldwide definition. Lancet. 2005, 366: 1059-62. 10.1016/S0140-6736(05)67402-8.
Paolo DP, Silvia C: Is transient elastography a useful tool for screening liver disease?. World J Gastroenterol. 2009, 15: 1409-1414. 10.3748/wjg.15.1409.
Matteoni CA, Younossi ZM, Gramlich T, Boparai N, Liu YC, McCllough AJ: Nonalcoholic fatty liver disease: A spectrum of clinical and pathological severity. Gastroenterology. 1999, 116: 1413-9. 10.1016/S0016-5085(99)70506-8.
Pi-Sunyer FX, Becker DM, Bouchard C, et al: Clinical Guidelines of the Identification, Evaluation, and Treatment of Overweight and Obesity in Adults. 1998, NIH Publication No.98-4083, Bethesda, MD: National Institutes of Health, 11-22.
Rudio C, Gil V, Belda J: Diagnostic efficacy of biological markers of alcohol consumption for the detection of excessive drinkers. An Med Interna. 1996, 13: 274-278.
Alta D, Ludemann J, Piek M: Distribution and dose response of laboratory markers to alcohol consumption in a general population: results of the study of health in Pomerania (SHIP). J Stud Alcohol. 2003, 64: 75-82.
Cook TA, Luczak SE, Shea SH: Associations of ALDH2 and ADH1B genotypes with response to alcohol in Asian Americans. J Stud Alcohol. 2005, 66: 196-204.
Chun-Tao W, Joel KG, Robert JF, Kalbfleisch JD, Marrero JA, Conjeevaram HS, Lok ASF: A simple noninvasive index can predict both significant fibrosis and cirrhosis in patients with chronic hepatitis C. Hepatology. 2003, 38: 518-526.
Arena U, Vizzutti F, Corti G, Ambu S, Stasi C, Bresci S, Moscarella S, Boddi V, Petrarca A, Laffi G, Marra F, Pinzani M: Acute viral hepatitis increases liver stiffness values measured by transient elastography. Hepatology. 2008, 47: 380-384. 10.1002/hep.22007.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-230X/11/70/prepub
We are grateful to Dr. Kiwamu Okita and Dr. Chihiro Sekiya for valuable suggestions.
The authors declare that they have no competing interests.
MB carried out this study, participated in the conception and design of the study. KF conceptualized, edited the manuscript for important intellectual content and has read and approved the final version of the manuscript. HB performed participated in the analysis and interpretation of the data. KK performed participated in the analysis and interpretation of the data. KS performed participated in the analysis and interpretation of the data. All authors read and approved the final manuscript.
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Baba, M., Furuya, K., Bandou, H. et al. Discrimination of individuals in a general population at high-risk for alcoholic and non-alcoholic fatty liver disease based on liver stiffness: a cross section study. BMC Gastroenterol 11, 70 (2011). https://doi.org/10.1186/1471-230X-11-70
- Body Mass Index
- Alcohol Consumption
- Fatty Liver
- Liver Fibrosis
- Nonalcoholic Fatty Liver Disease