# Clinical Significance of Lipoprotein Lipase (LPL) in People Living with HIV: A Comprehensive Assessment Including Lipidemia, Body Composition, Insulin Secretion, and Insulin Resistance

**Authors:** Akira Matsumoto, Kunio Yanagisawa, Yoshiyuki Ogawa, Takumi Nagasawa, Mayumi Nishiyama, Koji Sakamaki, Akihiro Yoshida, Masami Murakami, Katsuhiko Tsunekawa, Hiroshi Handa, Takao Kimura

PMC · DOI: 10.3390/nu17203207 · Nutrients · 2025-10-13

## TL;DR

This study explores how low levels of LPL in people with HIV are linked to poor lipid profiles and insulin issues, suggesting LPL could help guide treatment decisions.

## Contribution

The study identifies LPL as a novel predictor of dyslipidemia and insulin resistance in PLH on modern HIV therapy.

## Key findings

- Lower LPL levels and older age independently predict the need for antilipemic drugs in PLH.
- PLH have significantly lower HDL-C and higher HOMA-β compared to non-HIV controls.
- LPL levels below 65.3 ng/mL predict HDL-C < 40 mg/dL with high sensitivity.

## Abstract

Background/Objectives: Dyslipidemia is one of the major problems of long-term management in people living with human immunodeficiency virus (HIV) (PLH) as a risk factor for cardiovascular diseases. Lipoprotein lipase (LPL) is anchored on the surface of the capillary endothelial cells and plays a pivotal role in triglyceride metabolism by catabolizing dietary chylomicrons and very low-density lipoprotein synthesized in the liver. However, the details of the mechanisms in the era of integrase strand transfer inhibitor-based antiretroviral therapy have not yet been clarified. Methods: This study was a cross-sectional, single-center, non-interventional study evaluating the underlying factors associated with dyslipidemia, insulin resistance or secretion, and changes in the body composition of PLH. Results: Among PLH (n = 48), lower LPL (<60.8 ng/mL) and older age independently predicted antilipemic drug (ALD) necessity. A comparison of ALD-naïve PLH (n = 33) and age- and sex-matched non-HIV controls (n = 33) showed that PLH were significantly associated with lower high-density lipoprotein cholesterol (HDL-C) and higher HOMA-β. LPL was also the independent predictor of HDL-C < 40 mg/dL in PLH (adjusted odds ratio = 0.901, p = 0.044). Furthermore, LPL < 65.3 ng/mL predicted HDL-C < 40 mg/dL with 100% sensitivity and 60.9% specificity. Low levels of HIV-RNA were detected in the high HOMA-β group. Conclusions: In Japanese individuals, compared to non-HIV controls, PLH has low HDL-C and LPL. The measurement of LPL may confer the risk assessment and decision-making with relevance to ALD in PLH. Additionally, the effectiveness of HIV antiviral therapy and glucose tolerance may interact with each other.

## Linked entities

- **Proteins:** LPL (lipoprotein lipase)
- **Diseases:** dyslipidemia (MONDO:0002525)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** LPL (lipoprotein lipase) [NCBI Gene 4023] {aka HDLCQ11, LIPD}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** glucose tolerance (MESH:D018149), cardiovascular diseases (MESH:D002318), Lipidemia (MESH:D006949), Insulin Resistance (MESH:D007333), Dyslipidemia (MESH:D050171)
- **Chemicals:** triglyceride (MESH:D014280)
- **Species:** Human immunodeficiency virus (species) [taxon 12721], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12566720/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12566720/full.md

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Source: https://tomesphere.com/paper/PMC12566720