Evidence map›Paper›PMID 37415668›Full record

SynthesisFrontiers in endocrinology2023

Evidence of causality of low body mass index on risk of adolescent idiopathic scoliosis: a Mendelian randomization study.

Nao Otomo, Anas M Khanshour, Masaru Koido, Kazuki Takeda, Yukihide Momozawa, Michiaki Kubo, Yoichiro Kamatani, John A Herring, Yoji Ogura, Yohei Takahashi and 38 more

Abstract readMeta-Analysis
In one paragraph

Synthesis in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

48 authors.

Nao OtomoLaboratory for Statistical and Translational Genetics, RIKEN Center for Integrative Medical Sciences, RIKEN, Yokohama, Japan.
Anas M KhanshourCenter for Translational Research, Scottish Rite for Children, Dallas, TX, United States.
Masaru KoidoLaboratory for Statistical and Translational Genetics, RIKEN Center for Integrative Medical Sciences, RIKEN, Yokohama, Japan.
Kazuki TakedaDepartment of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Yukihide MomozawaLaboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Michiaki KuboLaboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Yoichiro KamataniDivision of Molecular Pathology, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
John A HerringDepartment of Orthopaedic Surgery , Scottish Rite for Children, Dallas, TX, United States.
Yoji OguraDepartment of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Yohei TakahashiDepartment of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Shohei MinamiDepartment of Orthopaedic Surgery, Seirei Sakura Citizen Hospital, Sakura, Japan.
Koki UnoDepartment of Orthopaedic Surgery, National Hospital Organization, Kobe Medical Center, Kobe, Japan.
Noriaki KawakamiDepartment of Orthopaedic Surgery, Meijo Hospital, Nagoya, Japan.
Manabu ItoDepartment of Orthopaedic Surgery, National Hospital Organization, Hokkaido Medical Center, Sapporo, Japan.
Tatsuya SatoDepartment of Orthopaedic Surgery, Juntendo University School of Medicine, Tokyo, Japan.
Kei WatanabeDepartment of Orthopaedic Surgery, Niigata University Medical and Dental General Hospital, Niigata, Japan.
Takashi KaitoDepartment of Orthopaedic Surgery, Osaka University Graduate School of Medicine, Suita, Japan.
Haruhisa YanagidaDepartment of Orthopaedic and Spine Surgery, Fukuoka Children's Hospital, Fukuoka, Japan.
Hiroshi TaneichiDepartment of Orthopaedic Surgery, Dokkyo Medical University School of Medicine, Mibu, Japan.
Katsumi HarimayaDepartment of Orthopaedic Surgery, Kyushu University Beppu Hospital, Beppu, Japan.
Yuki TaniguchiDepartment of Orthopaedic Surgery, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.
Hideki ShigematsuDepartment of Orthopaedic Surgery, Nara Medical University, Kashihara, Japan.
Takahiro IidaDepartment of Orthopaedic Surgery, Dokkyo Medical University Saitama Medical Center, Koshigaya, Japan.
Satoru DemuraDepartment of Orthopaedic Surgery Graduated School of Medical Science, Kanazawa University, Kanazawa, Japan.
Ryo SugawaraDepartment of Orthopaedic Surgery, Jichi Medical University, Shimotsuke, Japan.
Nobuyuki FujitaDepartment of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Mitsuru YagiDepartment of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Eijiro OkadaDepartment of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Naobumi HosoganeDepartment of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Katsuki KonoDepartment of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Masaya NakamuraDepartment of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Kazuhiro ChibaDepartment of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Toshiaki KotaniDepartment of Orthopaedic Surgery, Seirei Sakura Citizen Hospital, Sakura, Japan.
Tsuyoshi SakumaDepartment of Orthopaedic Surgery, Seirei Sakura Citizen Hospital, Sakura, Japan.
Tsutomu AkazawaDepartment of Orthopaedic Surgery, Seirei Sakura Citizen Hospital, Sakura, Japan.
Teppei SuzukiDepartment of Orthopaedic Surgery, National Hospital Organization, Kobe Medical Center, Kobe, Japan.
Kotaro NishidaDepartment of Orthopaedic Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Kenichiro KakutaniDepartment of Orthopaedic Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Taichi TsujiDepartment of Orthopaedic Surgery, Meijo Hospital, Nagoya, Japan.
Hideki SudoDepartment of Advanced Medicine for Spine and Spinal Cord Disorders, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Akira IwataDepartment of Preventive and Therapeutic Research for Metastatic Bone Tumor, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Satoshi InamiDepartment of Orthopaedic Surgery, Dokkyo Medical University School of Medicine, Mibu, Japan.
Carol A WiseCenter for Translational Research, Scottish Rite for Children, Dallas, TX, United States.
Yuta KochiDepartment of Genomic Function and Diversity, Medical Research Institute, Tokyo Medical and Dental and University, Tokyo, Japan.
Morio MatsumotoDepartment of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Shiro IkegawaLaboratory for Bone and Joint Diseases, RIKEN Center for Integrative Medical Sciences, Tokyo, Japan.
Kota WatanabeDepartment of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Chikashi TeraoLaboratory for Statistical and Translational Genetics, RIKEN Center for Integrative Medical Sciences, RIKEN, Yokohama, Japan.

Funding

Non-coding/epigenetic regulationP01HD084387 · NICHD · UT SOUTHWESTERN MEDICAL CENTER · PI Nadav Ahituv, LILIANNA SOLNICAKREZEL · 2016 to 2026
$14.2M
NICHD NIH HHS P01 HD084387
6 · The paper itself

Abstract

Introduction: Adolescent idiopathic scoliosis (AIS) is a disorder with a three-dimensional spinal deformity and is a common disease affecting 1-5% of adolescents. AIS is also known as a complex disease involved in environmental and genetic factors. A relation between AIS and body mass index (BMI) has been epidemiologically and genetically suggested. However, the causal relationship between AIS and BMI remains to be elucidated. Material and methods: Mendelian randomization (MR) analysis was performed using summary statistics from genome-wide association studies (GWASs) of AIS (Japanese cohort, 5,327 cases, 73,884 controls; US cohort: 1,468 cases, 20,158 controls) and BMI (Biobank Japan: 173430 individual; meta-analysis of genetic investigation of anthropometric traits and UK Biobank: 806334 individuals; European Children cohort: 39620 individuals; Population Architecture using Genomics and Epidemiology: 49335 individuals). In MR analyses evaluating the effect of BMI on AIS, the association between BMI and AIS summary statistics was evaluated using the inverse-variance weighted (IVW) method, weighted median method, and Egger regression (MR-Egger) methods in Japanese. Results: Significant causality of genetically decreased BMI on risk of AIS was estimated: IVW method (Estimate (beta) [SE] = -0.56 [0.16], p = 1.8 × 10 Conclusions: Our Mendelian randomization analysis using large studies of AIS and GWAS for BMI summary statistics revealed that genetic variants contributing to low BMI have a causal effect on the onset of AIS. This result was consistent with those of epidemiological studies and would contribute to the early detection of AIS.

Indexed as

Genome-Wide Association StudyScoliosisAdolescentBody Mass IndexHumansMendelian Randomization AnalysisPolymorphism, Single Nucleotideadolescent idiopathic scoliosisbody mass indexgenetic studygenome-wide association studyMendelian randomization (MR)

Identifiers

PMID37415668
PMCPMC10319580

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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.