Evidence map›Paper›PMID 32964145›Full record

ArticleJournal of clinical tuberculosis and other mycobacterial diseases2020

A pilot study on the genetic diversity of

Benjamin D Thumamo Pokam, D Yeboah-Manu, P M Teyim, P W Guemdjom, B Wabo, A B D Fankep, R E Okonu, Anne E Asuquo

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical tuberculosis and other mycobacterial diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.1field-weighted citation impact, top 53% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
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

8 authors at 3 institutions in 3 countries.

Benjamin D Thumamo PokamDepartment of Medical Laboratory Science, University of Buea, Cameroon.
D Yeboah-ManuNoguchi Memorial Institute for Medical Research, University of Ghana, Legon, Accra, Ghana.
P M TeyimDouala Tuberculosis Reference Laboratory, Littoral Region, Cameroon.
P W GuemdjomDepartment of Public Health, University of Buea, Cameroon.
B WaboDepartment of Medical Laboratory Science, University of Buea, Cameroon.
A B D FankepDepartment of Medical Laboratory Science, University of Buea, Cameroon.
R E OkonuNoguchi Memorial Institute for Medical Research, University of Ghana, Legon, Accra, Ghana.
Anne E AsuquoDepartment of Medical Laboratory Science, College of Medicine, University of Calabar, Calabar, Nigeria.
University of Buea · CMNoguchi Memorial Institute for Medical Research · GHUniversity of Calabar · NG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe re-emergence of tuberculosis (TB) worldwide, compounded by multi-drug resistance (MDR) of the causative agents constitutes a major challenge to the management of the disease. Rapid diagnosis and accurate strain identification are pivotal to the control of the disease. This pilot study investigated the genetic diversity of PATIENTS AND

methodsThis was a cross sectional hospital-based study carried out between January and December 2017 and including 158 isolates from sputum smear positive individuals [105 (66.5%) males and 53 (33.5%) females]. Sputum samples were tested using Xpert MTB/RIF, followed by culture on Lowenstein-Jensen medium. Isolates were further subjected to molecular characterization using

resultsThirteen (8.8%) of the 147 isolates with susceptibility results available were resistant to RIF. Drug resistance occurred in 5/50 (10%) female compared to 8/97 (8.2%) male (OR, 0.81; 0.25-2.62; p = 0.764), and there was no significant difference across the age ranges (p = 0.448). On the other hand, RIF resistance was associated (OR, 0.18, 95%CI, 0.05-0.69; p = 0.023) with previously treated patients [(4/14 (28.6%)] compared to new ones [9/133 (6.8%)]. The 150 identified lineages included among others 54 (36%) Cameroon, 18 (12%) UgandaI, 32 (21.3%) Haarlem, 17 (11.3%) Ghana, 9(6%) West African 1, 7(4.7%) Delhi/CAS, 4 (2.7%) LAM and 3 (2%) UgandaII. Of the 150 isolates, the major cluster was the Cameroon SIT 61, with 43(28.7%) isolates. Six (35.3%) of the 17 UgandaI sub-lineage were RIF resistant (OR, 9.58; 95%CI, 2.74-33.55, p = 0.001).

conclusionThe cosmopolitan Littoral region presents with a wide

Indexed as

CameroonRifampicin resistanceTuberculosisUgandaI sublineageXpert MTB/RIF

Identifiers

PMID32964145
PMCPMC7490731
OpenAlexW3082851457

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.