Evidence map›Paper›PMID 36185786›Full record

ArticleBiomedical reports2022

Direct‑acting antiviral treatment decreases serum undercarboxylated osteocalcin in male patients with chronic hepatitis C.

Tatsuki Ichikawa, Mio Yamashima, Shinobu Yamamichi, Makiko Koike, Yusuke Nakano, Tetsurou Honda, Hiroyuki Yajima, Osamu Miyazaki, Yasutaka Kuribayashi, Tomonari Ikeda and 2 more

Abstract read
In one paragraph

Article in Biomedical reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Observational
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.

Tatsuki IchikawaDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Nagasaki 850-8555, Japan.
Mio YamashimaDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Nagasaki 850-8555, Japan.
Shinobu YamamichiDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Nagasaki 850-8555, Japan.
Makiko KoikeInnovation and Translational Research Center, Nagasaki Harbor Medical Center, Nagasaki 850-8555, Japan.
Yusuke NakanoInnovation and Translational Research Center, Nagasaki Harbor Medical Center, Nagasaki 850-8555, Japan.
Tetsurou HondaDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Nagasaki 850-8555, Japan.
Hiroyuki YajimaDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Nagasaki 850-8555, Japan.
Osamu MiyazakiDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Nagasaki 850-8555, Japan.
Yasutaka KuribayashiDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Nagasaki 850-8555, Japan.
Tomonari IkedaDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Nagasaki 850-8555, Japan.
Takuma OkamuraDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Nagasaki 850-8555, Japan.
Kazuhiko NakaoDepartment of Gastroenterology and Hepatology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8501, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatic osteodystrophy (HOD) is a common complication of chronic liver disease, including viral hepatitis. Hepatitis C virus (HCV) infection is associated with an increased risk of osteoporosis and bone mineral density (BMD) loss. Direct-acting antiviral (DAA) treatment is used to treat HCV infections; however, its effects on bone metabolism have not been reported. We compared the clinical data and bone metabolic markers at the start of DAA treatment and 1 year later in 78 patients. There were 41 female and 37 male patients. HCV was successfully treated with DAA in all patients. Bone metabolic markers included undercarboxylated osteocalcin (ucOC), 25(OH) vitamin D (VD), total type I procollagen N-propeptide (P1NP), tartrate-resistant acid phosphatase 5b (TRACP-5b), and BMD. BMD was measured in the lumbar spine (mean, L2-L4) and femoral neck using dual-energy X-ray absorptiometry. ucOC in males decreased at 1 year after treatment initiation but not in females. In males, ucOC changes were related to alterations in proteins induced by vitamin K absence-II (PIVKA-II), hemoglobin A1c, and TRACP-5b, which contributed to P1NP and lumbar BMD at the start of DAA. Changes in ucOC among women contributed to the changes in grip strength and TRACP-5b levels. DAA treatment improved ucOC, a useful bone metabolic marker, in HCV-infected male patients. Changes in ucOC contributed to changes in PIVKA-II that likely ameliorated the vitamin K deficiency. DAA treatment has been reported to improve various extrahepatic disorders and abnormal bone metabolism, especially in HOD.

Indexed as

bone metabolic markerdirect-acting antivirushepatitis C virusundercarboxylated osteocalcin

Identifiers

PMID36185786
PMCPMC9523435

What OpenQuestion holds

Textmetadata
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.