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IGF-1

Insulin-like Growth Factor 1, Somatomedin C

Quick Stats
Studies 92
Trials 100
Score 3
2025 pubmed

Alterations of lipoprotein subfractions in GH-deficient adults.

Ratku. Balázs B; Lőrincz. Hajnalka H; Csiha. Sára S; Bíró. Lajos L; Erdei. Annamária A; Berta. Eszter E; Ujvárosy. Dóra D; Bodor. Miklós M; Nagy. Endre V EV; Szabó. Zoltán Z; Harangi. Mariann M; Somodi. Sándor S

Key Findings

  • GH‑deficient adults have altered lipoprotein subfractions (more IDL, smaller LDL, and a shift toward small HDL) despite normal standard lipid panels.
  • Higher IGF‑1 levels correlate positively with large and intermediate HDL and negatively with small HDL.
  • Short‑term GH withdrawal increases the smallest HDL (HDL‑6) and reinstating GH raises IDL percentages.

Practical Outcomes

  • For biohackers, measuring detailed HDL sub‑fractions could give a clearer picture of cardiovascular risk than standard cholesterol tests alone. Maintaining or modestly increasing IGF‑1 (through lifestyle, nutrition, or carefully supervised GH/IGF‑1 supplementation) may promote a healthier HDL profile. Any GH/IGF‑1 interventions should be done under medical supervision, as the study shows rapid lipid sub‑fraction changes with short‑term GH withdrawal.

Summary

In adults lacking growth hormone, the usual cholesterol numbers look normal, but detailed analysis shows hidden changes in the types of lipoproteins, especially the good‑cholesterol (HDL) particles. Higher IGF‑1 levels are linked to more large, protective HDL and fewer tiny, less‑protective HDL. Stopping GH for two months shifts these HDL sub‑types, and restarting it reverses some changes.

Abstract

Dyslipidemia is a common complication of adult growth hormone deficiency (AGHD) and considered an important contributor to increased mortality. Previous studies mainly focused on quantitative assessment of lipoproteins, but lipoprotein subfractions and their relationship with insulin-like growth factor 1 (IGF-1) have not been explored. To perform a comprehensive evaluation of lipoprotein subfractions and measuring apolipoprotein L1 (apoL1), sphingosine 1-phosphate (S1P) and apolipoprotein M (apoM) in AGHD. 11 GH-substituted (GHS) patients, 9 GH-unsubstituted (GHU) patients and 37 controls were included in the study. Lipoprotein subfractions were separated by the Lipoprint system. ApoL1, apoM and S1P were determined by ELISA. In the GHS patients GH-replacement was discontinued for 2 months. Measurements were performed before GH-discontinuation, at the end of the 2-month GH-withdrawal, and 1 month after reinstituting GH-replacement. Standard lipid parameters, apoM and apoL levels were not different between the groups. GHU patients demonstrated lower apolipoprotein A1 compared to controls (p=0.02) and higher apolipoprotein B100 compared to GHS (p=0.02). GHU and GHS showed higher S1P levels compared to controls (p=0.04 and p=0.01, respectively). Both GHU and GHS patients also presented higher percentage of intermediate-density lipoprotein (IDL) compared to controls (p=0.03 and p=0.01, respectively). Mean LDL size was lower in GHU compared to GHS (p=0.04). Percentage of intermediate HDL was lower in GHU and GHS compared to controls (p&lt;0.001 and p&lt;0.01, respectively). GHU demonstrated higher percentage of small HDL than controls (p&lt;0.001). Overall, log<sub>10</sub>IGF-1 correlated positively with the percentage of large HDL (r=0.27; p=0.04) and intermediate HDL (r=0.38; p&lt;0.01) and negatively with the percentage of small HDL (r=-0.46; p&lt;0.01). Log<sub>10</sub>IGF-1 was the best predictor of small HDL (standardized &#x3b2;=-0.46; p&lt;0.001) in overall subjects. In the GH-withdrawal study, the amount of HDL-6 increased with GH-withdrawal (p=0.03) and the percentage of IDL increased with reinstitution (p=0.05). Despite no changes in standard lipid parameters, considerable alterations of lipoprotein subfractions were revealed in GH-deficient adults indicating that lipoprotein subfraction analysis may allow for a more precise cardiovascular risk assessment in AGHD. Associations between HDL subfractions and Log<sub>10</sub>IGF-1 demonstrate a novel insight into the role of GH in lipid metabolism.

Study Information

Provider

pubmed

Year

2025

Date

2025-11-05T00:00:00.000Z

DOI

10.3389/fendo.2025.1696426

References

72