Evidence mapPaperPMID 34401527Full record

ArticleHealth science reports2021

Association of metformin use on metabolic acidosis in diabetic patients with chronic hepatitis B-related cirrhosis and renal impairment.

Terry Cheuk-Fung Yip, Raymond Ngai Chiu Chan, Vincent Wai-Sun Wong, Yee-Kit Tse, Lilian Yan Liang, Vicki Wing-Ki Hui, Xinrong Zhang, Guan-Lin Li, Henry Lik-Yuen Chan, Grace Lai-Hung Wong

Open access · goldAbstract read
In one paragraph

Article in Health science reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Guideline
  2. Article
  3. Article
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

10 authors at 2 institutions in 3 countries.

Terry Cheuk-Fung YipDepartment of Medicine and Therapeutics The Chinese University of Hong Kong Hong Kong China.ORCID https://orcid.org/0000-0002-1819-2464
Raymond Ngai Chiu ChanDepartment of Medicine and Therapeutics The Chinese University of Hong Kong Hong Kong China.
Vincent Wai-Sun WongDepartment of Medicine and Therapeutics The Chinese University of Hong Kong Hong Kong China.
Yee-Kit TseDepartment of Medicine and Therapeutics The Chinese University of Hong Kong Hong Kong China.
Lilian Yan LiangDepartment of Medicine and Therapeutics The Chinese University of Hong Kong Hong Kong China.
Vicki Wing-Ki HuiDepartment of Medicine and Therapeutics The Chinese University of Hong Kong Hong Kong China.
Xinrong ZhangDepartment of Medicine and Therapeutics The Chinese University of Hong Kong Hong Kong China.
Guan-Lin LiDepartment of Medicine and Therapeutics The Chinese University of Hong Kong Hong Kong China.
Henry Lik-Yuen ChanMedical Data Analytics Centre (MDAC) The Chinese University of Hong Kong Hong Kong China.
Grace Lai-Hung WongDepartment of Medicine and Therapeutics The Chinese University of Hong Kong Hong Kong China.
Chinese University of Hong Kong · HKUnion Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsMetformin is an oral anti-hyperglycemic recommended by the American Diabetes Association (ADA) as a preferred initial pharmacologic agent for type 2 diabetes. Metabolic acidosis is a rare yet severe side effect of it. We examined the association of metformin use and dosage on the risk of metabolic acidosis in diabetic patients with different degrees of chronic hepatitis B (CHB)-related cirrhosis and chronic kidney disease (CKD).

methodsMetabolic acidosis was defined by blood pH ≤7.35, together with lactate >5 mmol/L or arterial bicarbonate ≤18 mmol/L or venous bicarbonate ≤21 mmol/L, and/or diagnosis codes. Child-Pugh class and CKD stage were included in the model as time-dependent covariates. Age, gender, comorbidities, and use of relevant medications were adjusted as covariates. Maximum daily dose of metformin was classified into ≤1000 mg and >1000 mg.

resultsWe identified 4431 diabetic patients with CHB-related cirrhosis between 2000 and 2017 from a territory-wide database in Hong Kong. The risk of metabolic acidosis increased with Child-Pugh class B and C cirrhosis regardless of CKD stage (adjusted subdistribution hazard ratio [aSHR] ranged from 3.50 to 86.16). Metformin use was associated with a higher risk in patients with Child-Pugh class B or C cirrhosis and stage 3A CKD or above (aSHR ranged from 1.55 to 2.46). In stage 4/5 CKD, a daily dose of metformin ≤1000 mg was still associated with a higher risk of metabolic acidosis regardless of the severity of cirrhosis (aSHR ranged from 2.45 to 3.92).

conclusionIn conclusion, patients with Child-Pugh class B cirrhosis or above were at a higher risk of metabolic acidosis. Metformin further increased the risk in patients with Child-Pugh class B cirrhosis or above and stage 3A CKD or above. Dose adjustment in stage 4/5 CKD did not reduce the risk of metabolic acidosis.

Indexed as

Child‐Pugh scorechronic kidney diseaseshepatic complicationsmetabolic acidosismetformin

Identifiers

PMID34401527
PMCPMC8358231
OpenAlexW3194609101

What Socratic holds

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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 Socratic graph.