Evidence map›Paper›PMID 37463486›Full record

ArticleThe Journal of clinical endocrinology and metabolism2023

Nonalcoholic Fatty Liver Disease Incidence and Remission and Their Predictors During 7 Years of Follow-up Among Finns.

Satu Korpimäki, Suvi P Rovio, Markus Juonala, Nina Hutri-Kähönen, Terho Lehtimäki, Tomi P Laitinen, Päivi Tossavainen, Eero Jokinen, Britt-Marie Loo, Satu Männistö and 8 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

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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

18 authors at 9 institutions in 1 country.

Satu KorpimäkiDepartment of Clinical Physiology and Nuclear Medicine, Tampere University Hospital and Faculty of Medicine and Health Technology, Tampere University, 33100 Tampere, Finland.ORCID 0000-0002-2308-6180
Suvi P RovioResearch Centre of Applied and Preventive Cardiovascular Medicine, University of Turku, 20520 Turku, Finland.
Markus JuonalaDivision of Medicine, Turku University Hospital, 20521 Turku, Finland.ORCID 0000-0001-9498-364X
Nina Hutri-KähönenDepartment of Pediatrics, Tampere University Hospital and Faculty of Medicine and Health Technology, Tampere University, 33100 Tampere, Finland.
Terho LehtimäkiDepartment of Clinical Chemistry, Fimlab Laboratories and Faculty of Medicine and Health Technology, Finnish Cardiovascular Research Center-Tampere, Tampere University, 33100 Tampere, Finland.
Tomi P LaitinenDepartment of Clinical Physiology and Nuclear Medicine, Kuopio University Hospital and University of Eastern Finland, 70211 Kuopio, Finland.
Päivi TossavainenDepartment of Pediatrics and Adolescent Medicine, Oulu University Hospital, MRC Oulu and Research Unit of Clinical Medicine, University of Oulu, 90220 Oulu, Finland.
Eero JokinenDepartment of Pediatric Cardiology, Hospital for Children and Adolescents, University of Helsinki, 00290 Helsinki, Finland.
Britt-Marie LooJoint Clinical Biochemistry Laboratory, Turku University Hospital and University of Turku, 20500 Turku, Finland.
Satu MännistöDepartment of Chronic Disease Prevention, Finnish Institute for Health and Welfare, 00271 Helsinki, Finland.
Tuija TammelinLikes, School of Health and Social Studies, Jamk University of Applied Sciences, 40101 Jyväskylä, Finland.
Atte HaaralaDepartment of Clinical Physiology and Nuclear Medicine, Tampere University Hospital and Faculty of Medicine and Health Technology, Tampere University, 33100 Tampere, Finland.
Heikki AatolaDepartment of Clinical Physiology and Nuclear Medicine, Tampere University Hospital and Faculty of Medicine and Health Technology, Tampere University, 33100 Tampere, Finland.
Gaber KomarDepartment of Radiology, Turku University Hospital, 20521 Turku, Finland.
Jorma ViikariDivision of Medicine, Turku University Hospital, 20521 Turku, Finland.
Olli RaitakariResearch Centre of Applied and Preventive Cardiovascular Medicine, University of Turku, 20520 Turku, Finland.
Mika KähönenDepartment of Clinical Physiology and Nuclear Medicine, Tampere University Hospital and Faculty of Medicine and Health Technology, Tampere University, 33100 Tampere, Finland.
Katja PahkalaResearch Centre of Applied and Preventive Cardiovascular Medicine, University of Turku, 20520 Turku, Finland.
University of Turku · FITampere University Hospital · FIFinnish Institute for Health and Welfare · FIJAMK University of Applied Sciences · FIOulu University Hospital · FITampere University · FITurku University Hospital · FIUniversity of Eastern Finland · FIUniversity of Helsinki · FI

Funding

European Research Council 742927
6 · The paper itself

Abstract

contextThe incidence and remission of nonalcoholic fatty liver disease (NAFLD) are sparsely studied outside Asia.

objectiveThis prospective study aimed to investigate NAFLD incidence and remission, and their predictors among a general Finnish population.

methodsThe applied cohort included 1260 repeatedly studied middle-aged participants with data on liver ultrasound and no excessive alcohol intake. Hepatic steatosis was assessed by liver ultrasound with a 7.2-year study interval. Comprehensive data on health parameters and lifestyle factors were available.

resultsAt baseline, 1079 participants did not have NAFLD, and during the study period 198 of them developed NAFLD. Of the 181 participants with NAFLD at baseline, 40 achieved NAFLD remission. Taking multicollinearity into account, key predictors for incident NAFLD were baseline age (odds ratio 1.07; 95% CI, 1.02-1.13; P = .009), waist circumference (WC) (2.77, 1.91-4.01 per 1 SD; P < .001), and triglycerides (2.31, 1.53-3.51 per 1 SD; P < .001) and alanine aminotransferase (ALAT) (1.90, 1.20-3.00 per 1 SD; P = .006) concentrations as well as body mass index (BMI) change (4.12, 3.02-5.63 per 1 SD; P < .001). Predictors of NAFLD remission were baseline aspartate aminotransferase (ASAT) concentration (0.23, 0.08-0.67 per 1 SD; P = .007) and WC change (0.38, 0.25-0.59 per 1 SD; P < .001).

conclusionDuring follow-up, NAFLD developed for every fifth participant without NAFLD at baseline, and one-fifth of those with NAFLD at baseline had achieved NAFLD remission. NAFLD became more prevalent during the follow-up period. From a clinical perspective, key factors predicting NAFLD incidence and remission were BMI and WC change independent of their baseline level.

Indexed as

Non-alcoholic Fatty Liver DiseaseBody Mass IndexFinlandFollow-Up StudiesHumansIncidenceMiddle AgedProspective StudiesRisk Factorsdeterminantsgeneral populationincidencenonalcoholic fatty liver diseasepreventionremission

Identifiers

PMID37463486
PMCPMC10735312
OpenAlexW4384664057

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.