Evidence map›Paper›PMID 35759509›Full record

ArticlePLoS computational biology2022

Characterizing superspreading potential of infectious disease: Decomposition of individual transmissibility.

Shi Zhao, Marc K C Chong, Sukhyun Ryu, Zihao Guo, Mu He, Boqiang Chen, Salihu S Musa, Jingxuan Wang, Yushan Wu, Daihai He and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Inferring pathogen superspreading potential using early spatial spread patterns.medRxiv : the preprint server for health sciences · 2025
    Article
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  3. Observational
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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

11 authors at 4 institutions in 4 countries.

Shi ZhaoJC School of Public Health and Primary Care, Chinese University of Hong Kong, Hong Kong, China.ORCID 0000-0001-8722-6149
Marc K C ChongJC School of Public Health and Primary Care, Chinese University of Hong Kong, Hong Kong, China.ORCID 0000-0001-5610-1298
Sukhyun RyuDepartment of Preventive Medicine, Konyang University College of Medicine, Daejeon, South Korea.
Zihao GuoJC School of Public Health and Primary Care, Chinese University of Hong Kong, Hong Kong, China.ORCID 0000-0001-9002-0483
Mu HeDepartment of Foundational Mathematics, Xi'an Jiaotong-Liverpool University, Suzhou, China.ORCID 0000-0002-0085-7181
Boqiang ChenDepartment of Applied Mathematics, Hong Kong Polytechnic University, Hong Kong, China.ORCID 0000-0001-8726-4508
Salihu S MusaDepartment of Applied Mathematics, Hong Kong Polytechnic University, Hong Kong, China.ORCID 0000-0001-6335-2335
Jingxuan WangJC School of Public Health and Primary Care, Chinese University of Hong Kong, Hong Kong, China.ORCID 0000-0002-1570-7266
Yushan WuJC School of Public Health and Primary Care, Chinese University of Hong Kong, Hong Kong, China.ORCID 0000-0002-0687-1187
Daihai HeDepartment of Applied Mathematics, Hong Kong Polytechnic University, Hong Kong, China.ORCID 0000-0003-3253-654X
Maggie H WangJC School of Public Health and Primary Care, Chinese University of Hong Kong, Hong Kong, China.ORCID 0000-0003-1223-4595
Chinese University of Hong Kong · HKHong Kong Polytechnic University · HKKonyang University · KRXi’an Jiaotong-Liverpool University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the context of infectious disease transmission, high heterogeneity in individual infectiousness indicates that a few index cases can generate large numbers of secondary cases, a phenomenon commonly known as superspreading. The potential of disease superspreading can be characterized by describing the distribution of secondary cases (of each seed case) as a negative binomial (NB) distribution with the dispersion parameter, k. Based on the feature of NB distribution, there must be a proportion of individuals with individual reproduction number of almost 0, which appears restricted and unrealistic. To overcome this limitation, we generalized the compound structure of a Poisson rate and included an additional parameter, and divided the reproduction number into independent and additive fixed and variable components. Then, the secondary cases followed a Delaporte distribution. We demonstrated that the Delaporte distribution was important for understanding the characteristics of disease transmission, which generated new insights distinct from the NB model. By using real-world dataset, the Delaporte distribution provides improvements in describing the distributions of COVID-19 and SARS cases compared to the NB distribution. The model selection yielded increasing statistical power with larger sample sizes as well as conservative type I error in detecting the improvement in fitting with the likelihood ratio (LR) test. Numerical simulation revealed that the control strategy-making process may benefit from monitoring the transmission characteristics under the Delaporte framework. Our findings highlighted that for the COVID-19 pandemic, population-wide interventions may control disease transmission on a general scale before recommending the high-risk-specific control strategies.

Indexed as

Communicable DiseasesCOVID-19HumansLikelihood FunctionsModels, StatisticalPandemics

Identifiers

PMID35759509
PMCPMC9269899
OpenAlexW4283646773

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.