Long-term morbidity and mortality in patients diagnosed with an insulinoma

Author:

Peltola Elina12ORCID,Hannula Päivi13,Huhtala Heini4,Metso Saara13,Sand Juhani5,Laukkarinen Johanna15,Tiikkainen Mirja6,Sirén Jukka78,Soinio Minna9,Nuutila Pirjo1011,Moilanen Leena12,Laaksonen David E12,Ebeling Tapani1314,Arola Johanna1516,Schalin-Jäntti Camilla617,Jaatinen Pia123ORCID

Affiliation:

1. 1Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland

2. 2Division of Internal Medicine, Seinäjoki Central Hospital, Seinäjoki, Finland

3. 3Endocrinology, Department of Internal Medicine, Tampere University Hospital, Tampere, Finland

4. 4Faculty of Social Sciences, Tampere University, Tampere, Finland

5. 5Department of Gastroenterology and Alimentary Tract Surgery, Tampere University Hospital, Tampere, Finland

6. 6Endocrinology, Abdominal Center

7. 7Surgery, Abdominal Center, Helsinki University Hospital, Helsinki, Finland

8. 8Surgery, Abdominal Center, University of Helsinki, Helsinki, Finland

9. 9Department of Endocrinology, Division of Medicine, Turku University Hospital, Turku, Finland

10. 10Department of Endocrinology, Division of Medicine, Turku University Hospital, Turku, Finland

11. 11Turku PET Centre, University of Turku, Turku, Finland

12. 12Department of Medicine, Kuopio University Hospital, Kuopio, Finland

13. 13Faculty of Medicine, University of Oulu, Oulu, Finland

14. 14Endocrinology, Department of Medicine, Oulu University Hospital, Oulu, Finland

15. 15Pathology, HUSLAB, Helsinki University Hospital, Helsinki, Finland

16. 16Pathology, University of Helsinki, Helsinki, Finland

17. 17Endocrinology, Abdominal Center, University of Helsinki, Helsinki, Finland

Abstract

Objective Insulinomas are rare functional pancreatic neuroendocrine tumours. As previous data on the long-term prognosis of insulinoma patients are scarce, we studied the morbidity and mortality in the Finnish insulinoma cohort. Design Retrospective cohort study. Methods Incidence of endocrine, cardiovascular, gastrointestinal and psychiatric disorders, and cancers was compared in all the patients diagnosed with an insulinoma in Finland during 1980–2010 (n = 79, including two patients with multiple endocrine neoplasia type 1 syndrome), vs 316 matched controls, using the Mantel–Haenszel method. Overall survival was analysed with Kaplan–Meier and Cox regression analyses. Results The median length of follow-up was 10.7 years for the patients and 12.2 years for the controls. The long-term incidence of atrial fibrillation (rate ratio (RR): 2.07 (95% CI: 1.02–4.22)), intestinal obstruction (18.65 (2.09–166.86)), and possibly breast (4.46 (1.29–15.39) and kidney cancers (RR not applicable) was increased among insulinoma patients vs controls, P  < 0.05 for all comparisons. Endocrine disorders and pancreatic diseases were more frequent in the patients during the first year after insulinoma diagnosis, but not later on. The survival of patients with a non-metastatic insulinoma (n = 70) was similar to that of controls, but for patients with distant metastases (n = 9), the survival was significantly impaired (median 3.4 years). Conclusions The long-term prognosis of patients with a non-metastatic insulinoma is similar to the general population, except for an increased incidence of atrial fibrillation, intestinal obstruction, and possibly breast and kidney cancers. These results need to be confirmed in future studies. Metastatic insulinomas entail a markedly decreased survival.

Publisher

Bioscientifica

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

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