Pituitary & hypothalamus

Glucose metabolism, gut-brain hormones, and acromegaly treatment: an explorative single centre descriptive analysis

PituitaryPublished Descriptive study

Authors' conclusion

SSA impaired the insulin, glucagon, and incretin hormone secretions. Co-treatment with PEG seemed to counteract the somatostatinergic inhibition of the glucagon and insulin response to OGTT. We speculate that PEG may exert its action through GH-receptors on pancreatic δ-cells.

Study context

Population
Surgically treated, non-diabetic patients with acromegaly and healthy controls; Oral glucose tolerance test (OGTT) and isoglycaemic IV glucose infusion23 patients · 12 controls
Participants
15 / 4 / 11 / 12
Comparison
Acromegaly treatment regimens vs healthy controls
  • SSAn = 15
  • SSA + Pegvisomant (PEG)n = 4
  • SSA ÷ PEGn = 11reference
  • Healthy controlsn = 12reference
Outcome
Hormone responses to OGTT by treatment regimen
Methodological detailsexplorative, single-centre
  • Explorative
  • Single-centre

Main finding

As reported in the abstract

  • SSA: P = 0.001
  • SSA: P > 0.3

Further findings

OutcomeSSA + PEGSSA ÷ PEGP value
Insulin AUCSSA + PEG vs SSA ÷ PEG · increased with SSA + PEGmean 49 (SE 8.3) nmol/l*minmean 25 (SE 3.4)P = 0.007
Glucagon AUCSSA + PEG vs SSA ÷ PEG · increased with SSA + PEGmean 823 (SE 194) pmol/l*minmean 332 (SE 69)P = 0.009
GLP-1 secretionSSA + PEG vs SSA ÷ PEG · numerically increased with PEG3088 (SE 366) pmol/l*min2401 (SE 239)P = 0.3

GLP-1 secretion

GIP secretion remained significantly impaired with PEG

Radiotherapy and hydrocortisone substitution

No difference with/without radiotherapy nor with/without hydrocortisone substitution

Original publication

Glucose metabolism, gut-brain hormones, and acromegaly treatment: an explorative single centre descriptive analysis. Pituitary. Published 6 January 2023. doi:10.1007/s11102-022-01297-x

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