Peptides DB
Research-centric peptide and protocol reference hub
Study 11 of 29Pasireotide literaturebiorxiv-preprint · Observational2025

Prevalence, comorbidities and treatment outcomes of patients with Acromegaly in Qatar. Running title: Acromegaly in Qatar

This study highlights a prevalence of acromegaly in Qatar at 1.90 per 100,000, with over half of patients experiencing persistent disease despite surgery.

Read at biorxiv-preprintAdd to compare

Where it sits

this study against the rest of the pasireotide corpus
1
Preclinical
20
Observational · this one
0
Open-label
3
Randomised
5
Reviews

Summary and findings

This study measured the prevalence and treatment outcomes of patients with acromegaly in Qatar, involving 58 cases identified from a population of approximately 3.05 million. The study reported a prevalence of 1.90 per 100,000 and highlighted various comorbidities and treatment approaches, including a low rate of pasireotide use at 1.8%. The findings underscore the need for enhanced monitoring and treatment strategies in this population.

How much of this paper we could read: full text read (0.80). We had a clear abstract, so the summary below closely tracks the paper. What this means →
1.90 per 100,000 (95% CI: 1.41–2.39)2025

Abstract

The authors’ words, as biorxiv-preprint supplied them

<title>Abstract</title> <p><bold>Background</bold>: Acromegaly is associated with increased morbidity and reduced life expectancy. There are no previously published data on the presentation and management of patients with acromegaly in Qatar. <bold>Methods:</bold> This retrospective cohort study includes patients with acromegaly managed at Hamad Medical Corporation (HMC) between 1989 and 2024. <bold>Results:</bold> A total of 58 cases were identified in a population of ~3.05 million, yielding a prevalence of 1.90 per 100,000 (95% CI: 1.41–2.39). The mean age was 45.2±10.9 years, and 65.5% were male. The most common comorbidities were obesity (84.5%), diabetes (53.4%), and hypertension (46.6%). Tumor characteristics showed that 70.7% had macroadenomas and 12.1% had microadenomas, with a median tumor size of 14 mm (range: 11–18 mm). The most frequent histological subtype was GH-secreting adenomas (43.1%), followed by mixed GH & PRL adenomas (10.3%). Transsphenoidal surgery was performed in 87.9% of cases (52.9% at HMC, 47.1% outside Qatar), while 12.1% underwent pituitary radiotherapy. Medical therapy included octreotide (43.1%), cabergoline (32.8%), and pasireotide (1.8%), with no cases receiving pegvisomant. Postoperative MRI showed residual tumors in 41.4%, while 31.0% had no visible tumor, and MRI was not performed in 13.8%. Biochemical assessment indicated persistent disease in 53.4% of patients, while 32.8% achieved disease control, and data was not available for 13.8%. <bold>Conclusion:</bold> We report a high prevalence of acromegaly and associated comorbidities, and despite a high rate of transsphenoidal surgery, over half of patients have persistent disease, emphasizing the need for improved disease monitoring and treatment strategies in Qatar.</p>

Elsewhere in the Pasireotide corpus

BRecurrent Cushing's disease due to postoperative seeding of tumor cells in the sphenoid sinus: a case report with review of the literature.Endocrine journal · 2026 · n=1 · Not reported in abstract.HumanBPasireotide-LAR and pegvisomant combination in resistant acromegaly: a case series of predominantly mammosomatotroph adenomas.Pituitary · 2026 · n=6 · Median follow-up of 3.3 years (range 0.5 to 5.9).HumanBPredictors of in vitro response to somatostatin and dopamine receptor-targeted treatments are lacking in clinically non-functioning pituitary tumors.Journal of neuroendocrinology · 2023 · n=44 · No significant in vitro inhibition of cell proliferation was observed, ranging from -4.2% (OCT and PAS) to -7.4% (BIM-53097 + PAS).In vitroCPredictors of in vitro response to somatostatin and dopamine receptor-targeted treatments are lacking in clinically non-functioning pituitary tumors.Journal of neuroendocrinology · 2026 · No significant in vitro inhibition of cell proliferation was observed, ranging from -4.2% (OCT and PAS) to -7.4% (BIM-53097 + PAS).In vitroBApproach to the patient: precision medicine-guided evaluation and treatment of acromegaly.The Journal of clinical endocrinology and metabolism · 2026 · 80% of patients achieved hormonal control with biomarker-guided treatment.reviewBTirzepatide for pasireotide-induced hyperglycemia in a GH/TSH-producing pituitary adenoma/PitNET: a case report and literature review.Endocrine journal · 2026 · n=1 · HbA1c decreased from 7.7% to 6.3% after switching to tirzepatide.Human