Literature DB >> 29044586

Males with prolactinoma are at increased risk of incident cardiovascular disease.

Konstantinos A Toulis1,2, Tim Robbins3,4, Narendra Reddy5, Kumarendran Balachandran1, Krishna Gokhale1, Haren Wijesinghe1, Kar Keung Cheng1, Niki Karavitaki6,7, John Wass8, Krishnarajah Nirantharakumar1,6,7.   

Abstract

OBJECTIVE: To investigate whether the risk of incident cardiovascular disease (CVD) is increased in patients with prolactinoma.
DESIGN: Population-based, retrospective, open-cohort study using The Health Improvement Network (THIN) database. PATIENTS: A total of 2233 patients with prolactinoma and 10 355 matched controls (1:5 ratio) from UK General Practices contributing to THIN were included. Sex, age, body mass index and smoking status were used as matching parameters. The primary outcome was any incident CVD, defined by Read codes suggesting myocardial infarction, angina pectoris, stroke, transient ischaemic attack or heart failure. Sex-specific-adjusted incidence rate ratios (aIRRs) were calculated with Poisson regression, using clinically relevant parameters as model covariates. Sensitivity analyses were performed to check whether a change in the initial assumptions could have an impact on the findings.
RESULTS: During the 6-year observation period, the composite CVD outcome was recorded in 54 patients with prolactinoma and 180 "nonexposed" individuals. The incidence rate was 1.8 and 14.8 per 1000 person-years for the females and males with prolactinoma, respectively. The aIRRs for CVD were estimated at 0.99 [95% confidence interval (CI): 0.61-1.61, P = .968)] in female patients and 1.94 (95% CI: 1.29-2.91, P = .001) in male patients. These findings remained robust in sensitivity analyses restricting to patients with documented record of dopamine agonist treatment and those with newly diagnosed prolactinoma.
CONCLUSIONS: In contrast to females, men with prolactinoma have increased risk for incident CVD; the aetiology of this gender-specific finding remains to be elucidated.
© 2017 John Wiley & Sons Ltd.

Entities:  

Keywords:  cardiovascular disease; hyperprolactinaemia; pituitary adenoma; prolactinoma

Mesh:

Year:  2017        PMID: 29044586     DOI: 10.1111/cen.13498

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN: 0300-0664            Impact factor:   3.478


  4 in total

1.  Metabolic effects of dopamine agonists in patients with prolactinomas: a systematic review and meta-analysis.

Authors:  Sarah Byberg; Jesper Futtrup; Mikkel Andreassen; Jesper Krogh
Journal:  Endocr Connect       Date:  2019-10       Impact factor: 3.335

Review 2.  Hyperprolactinaemia.

Authors:  Irene Samperi; Kirstie Lithgow; Niki Karavitaki
Journal:  J Clin Med       Date:  2019-12-13       Impact factor: 4.241

3.  Metformin in the Treatment of Amisulpride-Induced Hyperprolactinemia: A Clinical Trial.

Authors:  Cuifang Zhu; Ruofan Li; Mingliang Ju; Xudong Xiao; Ti-Fei Yuan; Zhixing Jin; Jing Zhao
Journal:  Front Mol Neurosci       Date:  2022-05-26       Impact factor: 6.261

Review 4.  Large uremic toxins: an unsolved problem in end-stage kidney disease.

Authors:  Martin J Wolley; Colin A Hutchison
Journal:  Nephrol Dial Transplant       Date:  2018-10-01       Impact factor: 5.992

  4 in total

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