Evidence map›Paper›PMID 34992430›Full record

ArticlePharmacogenomics and personalized medicine2021

Isotretinoin Induced Hyperlipidemia and Impact of Leptin Gene

Amal A Mohamed, Alshymaa Hassnine, Amr Elsayed, Mahmoud Montaser, Yasmeen Ismail, Ahmed El-Demery, Eman Sultan, Rania S Abdel Aziz, Eman Eldemiry, Radwa Hagag and 2 more

Open access · goldAbstract read
In one paragraph

Article in Pharmacogenomics and personalized medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 21% 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, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Review
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

12 authors at 9 institutions in 1 country.

Amal A MohamedBiochemistry and Molecular Biology Department, National Hepatology & Tropical Medicine Research Institute, Cairo, Egypt.
Alshymaa HassnineGastroenterology and Tropical Medicine Department, Faculty of Medicine, Minia University, Minia, Egypt.ORCID 0000-0003-1352-0948
Amr ElsayedGastroenterology and Tropical Medicine Department, Faculty of Medicine, Minia University, Minia, Egypt.
Mahmoud MontaserDepartment of Dermatology, Andrology and STDs, Faculty of Medicine, Minia University, Minia, Egypt.
Yasmeen IsmailClinical Pharmacology Department, Faculty of Medicine, Benha University, Benha, Egypt.
Ahmed El-DemeryBiochemistry Department, Faculty of Medicine, October 6 University, 6th of October City, Egypt.
Eman SultanClinical Nutrition Department, National Nutrition Institute, Cairo, Egypt.
Rania S Abdel AzizClinical and Chemical Pathology Department, National Cancer Institute, Cairo University, Cairo, Egypt.
Eman EldemiryFaculty of Pharmacy, Fellow of Clinical Pharmacology, Cairo University Hospitals, Giza, Egypt.
Radwa HagagPharmacy Practice and Clinical Pharmacy Department, Faculty of Pharmacy, Egyptian Russian University, Badr City, Egypt.
Amal A El-KholyClinical Pharmacy Department, Faculty of Pharmacy, Ain Shams University, Cairo, Egypt.ORCID 0000-0003-4917-6392
Eman SalahDepartment of Dermatology, Andrology, Sexual Medicine and STDs, Faculty of Medicine, Helwan University, Cairo, Egypt.
Minia University · EGAin Shams University · EGBenha University · EGCairo University · EGCairo University hospitals · EGEgyptian Russian University · EGHelwan University · EGNational Water Research Center · EGOctober 6 University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcne vulgaris (AV) is a chronic inflammatory disease that affects the pilosebaceous unit. Leptin (LEP) gene polymorphisms is associated with higher risk of multiple disorders. Insulin-like growth factor-1 (IGF-1) exerts comedogenic effect by stimulating the sebaceous glands. Isotretinoin is an effective oral therapy for AV with many side effects including hyperlipidemia and increased serum levels of liver enzymes. PURPOSE: To evaluate the impact of LEP gene rs7799039 polymorphism in acne patients' clinical response lipid profile and liver enzymes following 6 months oral isotretinoin therapy in Egyptian AV patients.

methodsOne hundred eligible AV patients received 0.5 mg/kg oral isotretinoin for 6 months. Patients' demographics and clinical data were obtained. Body mass index (BMI), lipid profile, liver enzymes and IGF-1 were measured at baseline and after 6 months of therapy. Genotyping was done for LEP gene

resultsSix month administration of oral isotretinoin in Egyptian AV patients is associated with significantly elevated aspartate transaminase (AST) in CC and AC genotypes (P<0.001). Significant alanine aminotransferase (ALT) elevation was observed in CC, AC and AA genotypes (P <0.001, 0.004, 0.002, respectively). Total cholesterol (TC), triglycerides (TG) and low density lipoprotein (LDL) were elevated significantly P<0.001) in the three genotypes. IGF-1 was decreased significantly in CC and AC genotypes (P<0.001). CC genotype is associated with highest response (P<0.001).

conclusionLEP rs7799039 gene had an impact on the clinical response, lipid profile and liver enzymes in AV patients treated with oral isotretinoin. LEP rs7799039 CC genotype is predicted to be the treatment candidate for 6 month oral isotretinoin.

Indexed as

IGF-1insulin-like growth factor-1isotretinoinLEPleptinlipidliver enzymes

Identifiers

PMID34992430
PMCPMC8714009
OpenAlexW4200318821

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.