Evidence map›Paper›PMID 36676716›Full record

ArticleMedicina (Kaunas, Lithuania)2022

Evaluation of Hematological, Biochemical Profiles and Molecular Detection of Envelope Gene (gp-41) in Human Immunodeficiency Virus (HIV) among Newly Diagnosed Patients.

Asfa Anjum, Abaid Ur Rehman, Hina Siddique, Ali A Rabaan, Saad Alhumaid, Mohammed Garout, Souad A Almuthree, Muhammad A Halwani, Safaa A Turkistani, Haitham Qutob and 9 more

Open access · goldAbstract read
In one paragraph

Article in Medicina (Kaunas, Lithuania), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. 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

19 authors at 16 institutions in 4 countries.

Asfa AnjumDepartment of Medical Education, University of Lahore, Lahore 54590, Pakistan.
Abaid Ur RehmanDepartment of Medical Education, Sheikh Zayed Medical College, Rahim Yar Khan 06426, Pakistan.
Hina SiddiqueDepartment of Medical Education, Fatima Jinnah Medical University, Lahore 54000, Pakistan.
Ali A RabaanDepartment of Public Health and Nutrition, The University of Haripur, Haripur 22610, Pakistan.ORCID 0000-0002-6774-9847
Saad AlhumaidAdministration of Pharmaceutical Care, Al-Ahsa Health Cluster, Ministry of Health, Al-Ahsa 31982, Saudi Arabia.ORCID 0000-0003-4552-4513
Mohammed GaroutDepartment of Community Medicine and Health Care for Pilgrims, Faculty of Medicine, Umm Al-Qura University, Makkah 21955, Saudi Arabia.
Souad A AlmuthreeDepartment of Infectious Disease, King Abdullah Medical City, Makkah 43442, Saudi Arabia.
Muhammad A HalwaniDepartment of Medical Microbiology, Faculty of Medicine, Al Baha University, Al Baha 4781, Saudi Arabia.
Safaa A TurkistaniFakeeh College for Medical Science, Jeddah 21134, Saudi Arabia.ORCID 0000-0002-8607-5251
Haitham QutobDepartment of Medical Laboratory Technology, Faculty of Applied Medical Sciences, King Abdulaziz University, Rabigh 25732, Saudi Arabia.ORCID 0000-0003-2897-2250
Hawra AlbayatInfectious Disease Department, King Saud Medical City, Riyadh 7790, Saudi Arabia.
Mohammed AljeldahDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, University of Hafr Al Batin, Hafr Al Batin 39831, Saudi Arabia.ORCID 0000-0001-5335-2809
Basim R Al ShammariDepartment of Internal Medicine, College of Medicine, King Saud University, Riyadh 11362, Saudi Arabia.ORCID 0000-0002-3522-0607
Fatimah S AlshahraniDivision of Infectious Diseases, Department of Internal Medicine, College of Medicine, King Saud University and King Saud University Medical City, Riyadh 11451, Saudi Arabia.ORCID 0000-0002-4646-7488
Ali S AlghamdiDiagnostic Laboratory, Prince Sultan Military Medical City, Riyadh 12477, Saudi Arabia.
Sami M AlduwaihiDiagnostic Laboratory, Prince Sultan Military Medical City, Riyadh 12477, Saudi Arabia.
Adil A AlibraheemENT Department, Prince Sultan Military Medical City, Riyadh 12477, Saudi Arabia.
Shah ZebDepartment of Microbiology, Faculty of Biomedical and Health Science, The University of Haripur, Haripur 22610, Pakistan.
Basit ZeshanDepartment of Microbiology, Faculty of Life Sciences, University of Central Punjab, Lahore 54000, Pakistan.ORCID 0000-0001-5557-6523
Riyadh Armed Forces Hospital · SAAl Baha University · SAAlfaisal University · SAFatima Jinnah Medical University · PKKing Abdulaziz University · SAKing Abdullah Medical City · SAKing Saud Medical City · SAKing Saud University · SAMinistry of Health · MMShaikh Zayed Medical College and Hospital · PKSoliman Fakeeh Hospital · SAUmm al-Qura University · SAUniversiti of Malaysia Sabah · MYUniversity of Hafr Al-Batin · SAUniversity of Haripur · PKUniversity of Lahore · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Human Immunodeficiency Virus (HIV) is a highly morphic, retrovirus that rapidly evolves through mutation as well as recombination. Because of the immunocompromised status in HIV patients, there is often a higher chance of acquiring different secondary infections followed by liver cirrhosis, hepatitis B & C, and HIV-associated nephropathy. The current study was conducted to see the prevalence of secondary infections, hematological and biochemical markers for liver and renal associated diseases, and to detect the envelope gene (GP41) in newly diagnosed HIV patients. A total of 37 samples were collected from HIV-positive patients registered in different hospital settings under the National AIDS control program. The collected samples were processed for hepatitis B, hepatitis C, hematological analysis, and biochemical analysis. To identify the envelope gene in newly diagnosed HIV patients, polymerase chain reaction (PCR) was performed using four gene-specific primers. The HIV infections were seen more in male as compared to females. A significant decrease in complete blood count was observed in HIV patients when compared to healthy individuals. There was a significant increase in aspartate aminotransferase (AST), alanine aminotransferase (ALT), urea, and creatinine observed in HIV patients. No significant difference was observed in alkaline phosphatase (ALP), total bilirubin, and albumin levels when compared to healthy control. Anemia was observed in 59.4% of HIV patients. A total of three (8.1%) patients were found to be co-infected with hepatitis B and one (2.7 %) was co-infected with hepatitis C. Out of these 37 tested samples, a total of four showed the successful amplification of the envelope gene. This study provides platform for the health care facilitators to regularly monitor the signs, symptoms and clinical biomarkers of HIV-associated infections to prevent toxicity at an early stage to improve the quality of life (QoL) and minimize the mortality rate in HIV patients. Envelope gene mutating frequently results in drug resistance, and thus future research on polymorphism analysis will reveal points of substitutions to improve drug designing.

Indexed as

CoinfectionHepatitis BHepatitis CHIV InfectionsBiomarkersFemaleHepacivirusHIVHumansMalePrevalenceQuality of LifeBiomarkersAIDSblood-borne diseasescommunicable diseasesHBV-HIV co-infectionHCV-HIV co-infectionPakistanretrovirusrisk-factors

Identifiers

PMID36676716
PMCPMC9860646
OpenAlexW4313519117

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.