Evidence map›Paper›PMID 34704233›Full record

ArticleInternational journal of hematology2022

Identification of an asymptomatic Shwachman-Bodian-Diamond syndrome mutation in a patient with acute myeloid leukemia.

Sho Shibata, Shojiro Inano, Mizuki Watanabe, Kensuke Fujiwara, Hiroo Ueno, Yasuhito Nannya, Junya Kanda, Naoto Kawasaki, Yoshio Okamoto, Yoko Takiuchi and 5 more

Abstract readCase Reports
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In one paragraph

Article in International journal of hematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 38% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

15 authors at 3 institutions in 1 country.

Sho Shibata *Department of Hematology, Kitano Hospital, 2-4-20, Ougimachi, Kita-ku, Osaka, Japan.
Shojiro Inano *Department of Hematology, Kitano Hospital, 2-4-20, Ougimachi, Kita-ku, Osaka, Japan. shoin@kuhp.kyoto-u.ac.jp.ORCID http://orcid.org/0000-0003-0210-1158
Mizuki WatanabeDepartment of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Kensuke FujiwaraDepartment of Hematology, Hyogo Prefectural Amagasaki General Medical Center, Amagasaki, Japan.
Hiroo UenoDepartment of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Yasuhito NannyaDepartment of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Junya KandaDepartment of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Naoto KawasakiDepartment of Hematology, Kitano Hospital, 2-4-20, Ougimachi, Kita-ku, Osaka, Japan.
Yoshio OkamotoDepartment of Hematology, Kitano Hospital, 2-4-20, Ougimachi, Kita-ku, Osaka, Japan.
Yoko TakiuchiDepartment of Hematology, Kitano Hospital, 2-4-20, Ougimachi, Kita-ku, Osaka, Japan.
Akiko FukunagaDepartment of Hematology, Kitano Hospital, 2-4-20, Ougimachi, Kita-ku, Osaka, Japan.
Sumie TabataDepartment of Hematology, Kitano Hospital, 2-4-20, Ougimachi, Kita-ku, Osaka, Japan.
Seishi OgawaDepartment of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Akifumi Takaori-KondoDepartment of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Toshiyuki KitanoDepartment of Hematology, Kitano Hospital, 2-4-20, Ougimachi, Kita-ku, Osaka, Japan.
Kitano Hospital · JPKyoto University · JPHyogo Prefectural Amagasaki General Medical Center · JP

Funding

ministry of education, culture, sports, science and technology hp160219ministry of education, culture, sports, science and technology JP20cm0106501h0005
6 · The paper itself

Abstract

Shwachman-Diamond syndrome (SDS) is an autosomal recessive inherited disorder characterized by bone marrow failure, exocrine pancreatic dysfunction, and skeletal abnormalities. SDS is typically caused by a pathogenic mutation in the Shwachman-Bodian-Diamond Syndrome (SBDS) gene. Patients with SDS have an increased risk of developing acute myeloid leukemia (AML) and myelodysplastic syndromes. We identified germline biallelic SBDS mutations (p.K62X and p.I167M) in a 50-year-old AML patient who had never experienced the typical symptoms of SDS. The K62X mutation is one of the most common pathogenic mutations, whereas the significance of the I167M mutation was unclear. Based on cellular experiments, we concluded that the I167M mutation contributed to the development of AML, and chemotherapy including topoisomerase inhibitors, which induce DNA double-strand breaks, may have been toxic to this patient. Our experience indicates that some asymptomatic Shwachman-Bodian-Diamond syndrome mutations contribute to the development of leukemia, and that careful treatment selection may be warranted for patients harboring these mutations.

Indexed as

DNADNA RepairFemaleGenes, RecessiveGerm-Line MutationHumansLeukemia, Myeloid, AcuteMiddle AgedMyelodysplastic SyndromesProteinsShwachman-Diamond SyndromeTopoisomerase InhibitorsDNAProteinsSBDS protein, humanTopoisomerase InhibitorsAcute myeloid leukemiaDNA double-strand break repairShwachman–Diamond syndrome

Identifiers

PMID34704233
OpenAlexW3210424073

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.