Evidence map›Paper›PMID 42507316›Full record

Observational studyJournal of endocrinological investigation2026

Effect of metreleptin treatment in congenital generalized lipodystrophy: a retrospective analysis from the MENA region.

Majid Alfadhel, Afaf Alsagheir, Azza Al Shidhani, Ahmed Ali Nahari, Yasser Binafif, Najya Attia, Nasser Aljuhani, Khulood Najdeyah, Haya Alkhayyat, Jamal Al Jubeh and 11 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Journal of endocrinological investigation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

21 authors.

Majid AlfadhelMedical Genomic Research Department, King Abdullah International Medical Research Center (KAIMRC), King Saud Bin Abdulaziz University for Health Sciences (KSAU-HS), Ministry of National Guard Health Affairs (MNG-HA), Riyadh, Saudi Arabia. dralfadhelm@gmail.com.ORCID http://orcid.org/0000-0002-9427-7240
Afaf AlsagheirKing Faisal Specialist Hospital, Al Mathar Ash Shamali, Riyadh, Saudi Arabia.
Azza Al ShidhaniChild Health Department, Sultan Qaboos University Hospital, University Medical City, Sultan Qaboos University, Muscat, Oman.
Ahmed Ali NahariJazan Specialist Hospital, Jazan Health Cluster, Jazan, Saudi Arabia.
Yasser BinafifEast Jeddah Hospital, King Abdallah Rd, Al Sulaymaniyah, Jeddah, Saudi Arabia.
Najya AttiaKing Saud bin Abdulaziz University for Health Sciences, Department of Pediatrics, King Abdullah Specialist Children Hospital, King Abdullah International Medical Research Center, Ministry of National Guard Health Affairs, Jeddah, Saudi Arabia.
Nasser AljuhaniEast Jeddah Hospital, King Abdallah Rd, Al Sulaymaniyah, Jeddah, Saudi Arabia.
Khulood NajdeyahKing Abdulaziz Hospital, Jeddah, Saudi Arabia.
Haya AlkhayyatMilitary Hospital, BDF Royal Medical Services, Riffa, Bahrain.
Jamal Al JubehSheikh Khalifa Medical City, Al Karamah St, Al Manhal, Abu Dhabi, United Arab Emirates.
Imad BremaKing Fahad Medical City, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
Najah DoubaKing Saud Medical City, Riyadh, Saudi Arabia.
Elham AlamiriSulaiman Alhabib Hospital, DHCC, Dubai, United Arab Emirates.
Mouza Al YahyaeiNational Diabetes and Endocrine Center, Royal Hospital, Ministry of Health, Muscat, Sultanate of Oman.
Saleha BabliPrince Sultan Military Medical City, Riyadh, Saudi Arabia.
Mohammed AlqahtaniAbha Maternity and Children Hospital, Abha, Saudi Arabia.
Amal Al-QahtaniAbha Maternity and Children Hospital, Abha, Saudi Arabia.
Ibrahim Al AlwanMedical Genomic Research Department, King Abdullah International Medical Research Center (KAIMRC), King Saud Bin Abdulaziz University for Health Sciences (KSAU-HS), Ministry of National Guard Health Affairs (MNG-HA), Riyadh, Saudi Arabia.
Nadia HergliChiesi Farmaceutici, Parma, Italy.
Saif Al YaarubiOman Medical Specialty Board, Muscat, Oman.
Rebecca J BrownNational Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD, USA.

Funding

Chiesi Farmaceutici Chiesi Farmaceutici
6 · The paper itself

Abstract

purposeCongenital generalized lipodystrophy (CGL) is characterized by near-total loss of body fat, leptin deficiency, and severe metabolic complications. Clinical data show that metreleptin improves metabolic control in CGL; however, data from the Middle East and North Africa (MENA) is limited. We assessed the real-world effectiveness and safety of metreleptin in patients with CGL from this region.

methodsWe conducted a multicenter, retrospective chart review of patients with CGL. Baseline, 6 ± 2months (short-term), 2 ± 1years (long-term), and >3 years follow-up data were analyzed. Median changes from baseline were calculated for short- and long-term assessments; >3 years data were reviewed individually. Safety was evaluated up to 90 days after last dose.

resultsThirty-eight patients were included (82% female; median age at baseline, 6.3 years). Median treatment duration with metreleptin was 25 months (max dose, 10 mg/day). Significant short-term median reductions from baseline were observed for HbA1c (- 1.4%; n = 26), fasting plasma glucose (- 0.5 mmol/L; n = 21); fasting triglycerides (TG; -1.5 mmol/L; n = 26), alanine aminotransferase (- 18 IU/L, n = 27) and aspartate aminotransferase (- 7 IU/L, n = 27) (all p ≤ 0.02). These reductions were significant at long-term follow-up (p < 0.01) except for aspartate aminotransferase. At short-term follow-up, 50.0% of patients achieved  ≥1%  reduction in HbA1c and 65.4% had a  ≥30% reduction in TG; corresponding long-term patient proportions were 46.7% and 61.5%. Most patients with >3 years follow-up showed improvement/maintenance of metabolic parameters. Overall, metreleptin was well tolerated with no new safety signals detected.

conclusionsOur findings support early intervention with metreleptin for sustained diabetes and hypertriglyceridemia control in CGL.

Indexed as

BiomarkersLeptinLipodystrophy, Congenital GeneralizedAfrica, NorthernBlood GlucoseChildChild, PreschoolFemaleFollow-Up StudiesGlycated HemoglobinHumansMaleMiddle EastPrognosisRetrospective StudiesTreatment OutcomeBiomarkersBlood GlucoseGlycated HemoglobinLeptinmetreleptinCongenital generalized lipodystrophyHbA1cMetabolic diseaseMetreleptinTriglycerides

Identifiers

PMID42507316
PMCPMC13627170

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.