Evidence map›Paper›PMID 33692422›Full record

ArticleScientific reports2021

A Chinese multicenter retrospective study of isolated increased nuchal translucency associated chromosome anomaly and prenatal diagnostic suggestions.

Hua Jin, Juan Wang, Guoying Zhang, Hongyan Jiao, Jiansheng Zhu, Zhimin Li, Chen Chen, XuanPing Zhang, Huan Huang, JiaYin Wang

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

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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

10 authors at 6 institutions in 1 country.

Hua Jin *Department of Prenatal Diagnosis, Ji'nan Maternal and Child Health Care Hospital, Ji'nan, Shandong, China.
Juan Wang *School of Computer Science and Technology, Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Guoying ZhangDepartment of Obstetrics and Gynecology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Hongyan JiaoDepartment of The Branch Center of Prenatal Diagnosis, Shijiazhuang Maternal and Child Care Service Hospital, Shijiazhuang, Hebei, China.
Jiansheng ZhuMedical Genetic Center, Maternity and Child Health Hospital of Anhui Province, Affiliated Maternity and Child Health Hospital of Anhui Medical University, Anhui, China.
Zhimin LiSchool of Computer Science and Technology, Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Chen ChenZhejiang Annoroad Biotechnology Co., Ltd, Zhejiang, China.
XuanPing ZhangSchool of Computer Science and Technology, Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Huan HuangDepartment of Obstetrics and Gynecology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China. huanghuan@njmu.edu.cn.
JiaYin WangSchool of Computer Science and Technology, Xi'an Jiaotong University, Xi'an, Shaanxi, China. wangjiayin@mail.xjtu.edu.cn.
Xi'an Jiaotong University · CNAnhui Medical University · CNAnnoroad Gene Technology (China) · CNFirst Hospital of Shijiazhuang · CNJiangsu Province Hospital · CNNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extensive researches involving fetuses with multiple ultrasound anomalies have been conducted over the years, but only few were focused on the isolated increased nuchal translucency (NT). On top of that, these limited number of researches were all designed as single-arm studies and the control group was missing. In this study, we conducted a multicenter, retrospective study using amniotic fluid samples collected from 1197 pregnant women having fetuses with isolated increased NT (INT group) or normal NT values (NNT group). Copy number variation sequencing (CNV-seq) was performed to determine their chromosome status and pathogenic variations were validated using SNP array. Overall, 59 chromosome aneuploidies, 34 pathogenic CNVs and 23 copy number variants of unknown significance (VOUS CNVs) were discovered. the INT group had a significantly higher proportion of aneuploidy (19.44%) and pathogenic CNV (8.33%) than the control group (3.49% and 2.30% respectively), and 88.89% of the pathogenic CNVs were related to heart defects. Additionally, more male fetuses were presented in the INT group (68.51%), but they did not have a higher risk (Relative Risk = 1.03) of carrying pathogenic chromosome variations than female fetuses. Our results demonstrated that fetuses with isolated increased NT had a distinct pattern of chromosome abnormality and majority of detected pathogenic CNVs could be linked to the congenital heart disease. Furthermore, because a considerable proportion of pathogenic CNVs were detected, we strongly recommend to perform a joint test of karyotyping and CNV analysis in prenatal diagnosis for fetuses with isolated increased NT in order to decrease the incident of missed diagnosis.

Indexed as

AneuploidyChromosome DisordersDNA Copy Number VariationsNuchal Translucency MeasurementPrenatal DiagnosisFemaleHumansMalePregnancy

Identifiers

PMID33692422
PMCPMC7947009
OpenAlexW3176400667

What OpenQuestion holds

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Registered trials

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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.