Evidence map›Paper›PMID 32822391›Full record

ArticlePloS one2020

Clinical spectrum of non-alcoholic fatty liver disease in patients with diabetes mellitus.

Kaina Chen, Wei Kwan Sng, Joanne Hui-Min Quah, Jin Liu, Bee Yen Chong, Hwee Khim Lee, Xue Fei Wang, Ngiap Chuan Tan, Pik-Eu Chang, Hong Chang Tan and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.9field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
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  8. The impact of obesity: a narrative review.Singapore medical journal · 2023
    Review
  9. Article
  10. Article
  11. Article
  12. Fatty Liver Disease-Alcoholic and Non-Alcoholic: Similar but Different.International journal of molecular sciences · 2022
    Review
  13. Article
  14. Article
  15. Article
  16. Noninvasive, Blood-Based Biomarkers as Screening Tools for Hepatic Fibrosis in People With Type 2 Diabetes.Clinical diabetes : a publication of the American Diabetes Association · 2022
    Article
  17. Review
  18. Article
  19. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Kaina ChenDepartment of Gastroenterology & Hepatology, Singapore General Hospital, Singapore, Singapore.ORCID 0000-0002-0778-7294
Wei Kwan SngSingHealth Polyclinics, Singapore, Singapore.
Joanne Hui-Min QuahDuke NUS Medical School, Singapore, Singapore.
Jin LiuDuke NUS Medical School, Singapore, Singapore.
Bee Yen ChongSingHealth Polyclinics, Singapore, Singapore.
Hwee Khim LeeSingHealth Polyclinics, Singapore, Singapore.
Xue Fei WangSingHealth Polyclinics, Singapore, Singapore.
Ngiap Chuan TanDuke NUS Medical School, Singapore, Singapore.
Pik-Eu ChangDepartment of Gastroenterology & Hepatology, Singapore General Hospital, Singapore, Singapore.
Hong Chang TanDepartment of Endocrinology, Singapore General Hospital, Singapore, Singapore.
Yong Mong BeeDepartment of Endocrinology, Singapore General Hospital, Singapore, Singapore.
George Boon Bee GohDepartment of Gastroenterology & Hepatology, Singapore General Hospital, Singapore, Singapore.
SingHealth Polyclinics · SGSingapore General Hospital · SGDuke-NUS Medical School · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNon-alcoholic fatty liver disease (NAFLD) is increasingly widespread with an overall global estimated prevalence of 25%. Type 2 diabetes Mellitus (T2DM) is a key contributor to NAFLD progression and predicts moderate-severe liver fibrosis and mortality. However, there is currently no uniform consensus on routine NAFLD screening among T2DM patients, and the risk factors of NAFLD and advanced fibrosis among T2DM patients remain to be clarified fully.

aimWe explored the prevalence, clinical spectrum, and risk factors of NAFLD and liver fibrosis among T2DM patients.

methodsThis is a cross-sectional study that enrolled subjects from a primary care clinic and a diabetes centre in Singapore. Subjects aged 21 to 70 years of all ethnic groups with an established T2DM diagnosis were included. Subjects with chronic liver diseases of other aetiologies were excluded. All subjects underwent transient elastography for hepatic steatosis and fibrosis assessment. Their demographics, anthropometric measurements and clinical parameters were collected. Statistical analysis was performed using STATA/SE16.0 software.

resultsAmong 449 enrolled T2DM subjects, 436 with complete data and valid transient elastography results were analysed. Overall, 78.72% (344/436) of the T2DM subjects had NAFLD, of which 13.08% (45/344) had increased liver stiffness. Higher ALT level (OR = 1.08; 95% CI: 1.03-1.14; p = 0.004), obesity (BMI ≥ 27.5 kg/m2, OR = 2.64; 95% CI: 1.28-5.44; p = 0.008) and metabolic syndrome (OR = 4.36; 95% CI 1.40-13.58; p = 0.011) were independent factors associated with increased CAP (NAFLD). Higher AST level (OR = 1.06; 95% CI: 1.02-1.11; p = 0.008), CAP value (OR = 1.02; 95% CI: 1.00-1.03; p = 0.003), lower platelet count (OR = 0.99; 95% CI: 0.98-1.00; p = 0.009) and concomitant hypertension (OR = 4.56; 95% CI: 1.18-17.62; p = 0.028) were independent factors associated with increased liver stiffness.

conclusionsOur study demonstrated a considerably high prevalence of NAFLD among T2DM patients, with the proportion of advanced liver fibrosis among T2DM NAFLD patients much higher than the general population. Given that NAFLD is largely asymptomatic, increased awareness and vigilance for identifying NAFLD and increased liver stiffness among T2DM patients should be advocated.

Indexed as

AdultAgedCross-Sectional StudiesDiabetes Mellitus, Type 2Elasticity Imaging TechniquesFemaleHumansLiver CirrhosisMaleMiddle AgedNon-alcoholic Fatty Liver DiseasePrevalenceRisk FactorsSingaporeYoung Adult

Identifiers

PMID32822391
PMCPMC7446805
OpenAlexW3080104603

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.