Evidence map›Paper›PMID 40459998›Full record

Trial reportAging cell2025

Nicotinamide Riboside Supplementation Benefits in Patients With Werner Syndrome: A Double-Blind Randomized Crossover Placebo-Controlled Trial.

Mayumi Shoji, Hisaya Kato, Masaya Koshizaka, Hiyori Kaneko, Yusuke Baba, Takahiro Ishikawa, Naoya Teramoto, Daisuke Kinoshita, Ayano Yamaguchi, Yukari Maeda and 6 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Aging cell, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Review
  6. NADNature metabolism · 2025
    Review
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

16 authors.

Mayumi ShojiDepartment of Endocrinology, Hematology and Gerontology, Chiba University Graduate School of Medicine, Chiba, Japan.
Hisaya KatoDepartment of Endocrinology, Hematology and Gerontology, Chiba University Graduate School of Medicine, Chiba, Japan.
Masaya KoshizakaDepartment of Endocrinology, Hematology and Gerontology, Chiba University Graduate School of Medicine, Chiba, Japan.ORCID 0000-0001-7374-9993
Hiyori KanekoDepartment of Endocrinology, Hematology and Gerontology, Chiba University Graduate School of Medicine, Chiba, Japan.
Yusuke BabaDepartment of Endocrinology, Hematology and Gerontology, Chiba University Graduate School of Medicine, Chiba, Japan.
Takahiro IshikawaDepartment of Endocrinology, Hematology and Gerontology, Chiba University Graduate School of Medicine, Chiba, Japan.
Naoya TeramotoDepartment of Endocrinology, Hematology and Gerontology, Chiba University Graduate School of Medicine, Chiba, Japan.
Daisuke KinoshitaDepartment of Endocrinology, Hematology and Gerontology, Chiba University Graduate School of Medicine, Chiba, Japan.
Ayano YamaguchiDepartment of Endocrinology, Hematology and Gerontology, Chiba University Graduate School of Medicine, Chiba, Japan.
Yukari MaedaDepartment of Endocrinology, Hematology and Gerontology, Chiba University Graduate School of Medicine, Chiba, Japan.
Yosuke InabaClinical Research Center, Chiba University Hospital, Chiba, Japan.
Yuki ShikoClinical Research Center, Chiba University Hospital, Chiba, Japan.
Yoshihito OzawaClinical Research Center, Chiba University Hospital, Chiba, Japan.
Vilhelm A BohrLaboratory of Molecular Gerontology, National Institute on Aging, NIH, Baltimore, Maryland, USA.ORCID 0000-0003-4823-6429
Yoshiro MaezawaDepartment of Endocrinology, Hematology and Gerontology, Chiba University Graduate School of Medicine, Chiba, Japan.
Koutaro YokoteDepartment of Endocrinology, Hematology and Gerontology, Chiba University Graduate School of Medicine, Chiba, Japan.

Funding

Japan Agency for Medical Research and Development JP21jm0210096Japan Agency for Medical Research and Development JP22ym0126066Japan Agency for Medical Research and Development JP23ek0109622Japan Agency for Medical Research and Development JP24ek0109713Japan Society for the Promotion of Science JP21K19437Japan Society for the Promotion of Science JP22KK0284Japan Society for the Promotion of Science JP23H00417Japan Society for the Promotion of Science JP23K14705Japan Society for the Promotion of Science JP24K10525the Ministry of Health, Labour and Welfare Research on Rare and Intractable Diseases Program JP21FC1016the Ministry of Health, Labour and Welfare Research on Rare and Intractable Diseases Program JP21FC2001the Ministry of Health, Labour and Welfare Research on Rare and Intractable Diseases Program JP24FC1013
6 · The paper itself

Abstract

Werner syndrome (WS) is a rare hereditary progeroid syndrome caused by mutations in the WRN gene. Patients frequently develop various age-associated diseases prematurely, often leading to early mortality (≤ 60 years of age). Depletion of nicotinamide adenine dinucleotide (NAD)

Indexed as

Dietary SupplementsNiacinamideWerner SyndromeAdultCross-Over StudiesDouble-Blind MethodFemaleHumansMaleMiddle AgedPyridinium CompoundsNiacinamidenicotinamide-beta-ribosidePyridinium Compoundsarterial stiffnesscardio–ankle vascular indexcreatinineintractable skin ulcersmetabolomenicotinamide ribosideWerner syndrome

Identifiers

PMID40459998
PMCPMC12341770

What OpenQuestion holds

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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.