# Inflammation, Endothelial Dysfunction and Increased Left Ventricular Mass in Chronic Kidney Disease (CKD) Patients: A Longitudinal Study

**Authors:** Kyriakos Ioannou, Vianda S. Stel, Evangelia Dounousi, Kitty J. Jager, Aikaterini Papagianni, Konstantinos Pappas, Kostas C. Siamopoulos, Carmine Zoccali, Dimitrios Tsakiris

PMC · DOI: 10.1371/journal.pone.0138461 · PLoS ONE · 2015-09-23

## TL;DR

This study shows that inflammation and endothelial dysfunction are linked to increased heart muscle mass in patients with chronic kidney disease.

## Contribution

The study provides new evidence on the longitudinal relationship between inflammation, endothelial dysfunction, and left ventricular mass in predialysis CKD patients.

## Key findings

- Higher IL-6 and inflammation scores were associated with increased left ventricular mass indexed for height.
- VCAM-1 was also linked to higher left ventricular mass in CKD patients.
- Adjustments for diuretic use and other confounders confirmed the associations.

## Abstract

Within this longitudinal study we investigated the association of inflammation markers C-reactive protein (CRP), interleukin-6 (IL-6) and tumor necrosis factor-α (TNFα) and endothelial dysfunction markers intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) with left ventricular mass indexed for height2·71 (LVMI) in hypertensive predialysis CKD patients.

From 2004 to 2005, 182 incident consecutive adult patients from the outpatient CKD clinics of two hospitals in Greece with CKD and hypertension or using antihypertensive medication, were included. Of these, 107 patients underwent CRP (mg/l) and LVMI (g/height2·71) measurements annually for three years.

In the longitudinal analyses, using linear mixed modeling, a higher IL-6 (ß = 1.9 (95%ci:0.38;3.5), inflammation score based on CRP, IL-6 and TNF-α (ß = 5.0 (95%ci:0.72; 9.4) and VCAM-1 (ß = 0.01 (95%ci:0.005;0.02) were associated with higher LVMI. These models were adjusted for age, gender and primary renal disease, and for confounders that on top changed the beta with ≥10%, i.e. diuretic use (for IL-6 and inflammation score).

The results suggest that in predialysis CKD patients, inflammation as well as endothelial dysfunction may play an important role towards the increase in LVMI.

## Linked entities

- **Proteins:** IL6 (interleukin 6)
- **Diseases:** chronic kidney disease (MONDO:0005300)

## Full-text entities

- **Genes:** Ren (renin) [NCBI Gene 24715] {aka RATRENAA, RENAA, Ren1}, ICAM1 (intercellular adhesion molecule 1) [NCBI Gene 3383] {aka BB2, CD54, P3.58}, Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 59086] {aka Tgfb}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, VCAM1 (vascular cell adhesion molecule 1) [NCBI Gene 7412] {aka CD106, INCAM-100}, Agt (angiotensinogen) [NCBI Gene 24179] {aka ANRT, Ang, AngII, PAT}, Nppb (natriuretic peptide B) [NCBI Gene 25105] {aka BNP, Bnf}
- **Diseases:** ischemic heart disease (MESH:D017202), infection (MESH:D007239), heart failure (MESH:D006333), myocardial hypertrophy (MESH:D006984), atherosclerosis (MESH:D050197), Endothelial Dysfunction (MESH:D014652), CKD (MESH:D051436), Ventricular Mass (MESH:C536030), Inflammation (MESH:D007249), obesity (MESH:D009765), diabetic (MESH:D003920), essential (MESH:D020329), cardiovascular disease (MESH:D002318), pressure and volume overload (MESH:D019190), Hypertension (MESH:D006973), myocardial infarction (MESH:D009203), ventricular (MESH:D014693), renal function decline (MESH:D060825), myocardial disorders (MESH:D009202), LVH (MESH:D017379), stroke (MESH:D020521), albuminuria (MESH:D000419), vascular damage (MESH:D057772), fibrosis (MESH:D005355), Kidney Disease (MESH:D007674), LVM (MESH:D018487), anemia (MESH:D000740), malignancy (MESH:D009369)
- **Chemicals:** Lipids (MESH:D008055), salt (MESH:D012492), ace (MESH:C024789), ace or arb (-),  (MESH:D015415),  (MESH:D019010),  (MESH:C508600),  (MESH:D014409),  (MESH:D015850)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** -174G/C

## Full text

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## Figures

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## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC4580570/full.md

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Source: https://tomesphere.com/paper/PMC4580570