# Ongoing and Novel Challenges in Kidney Transplantation: Therapeutic Approaches to Non-Immunological Risk Factors for Allograft Loss

**Authors:** Michele Provenzano, Roberta Arena, Ida Gagliardi, Lilio Hu, Chiara Ruotolo, Gemma Patella, Giuseppe Pezzi, Rosita Greco, Valeria Grandinetti, Rocco Malivindi, Michele Di Dio, Olga Baraldi, Giorgia Comai, Luca De Nicola

PMC · DOI: 10.3390/life16020248 · Life · 2026-02-02

## TL;DR

This paper reviews non-immunological risk factors like hypertension and diabetes that affect kidney transplant success and explores their clinical impact and management.

## Contribution

The paper provides a focused review of non-immunological factors most closely linked to chronic kidney disease in transplant recipients.

## Key findings

- Hypertension is reported in 90% of kidney transplant recipients and is strongly linked to reduced graft survival.
- Anemia affects 20–51% of patients and contributes to cardiovascular issues and graft dysfunction.
- Proteinuria prevalence ranges from 7.5% to 45% and is a significant negative prognostic factor.

## Abstract

In recent decades, the rate of kidney transplantation has risen significantly, leading to better outcomes in terms of cardiovascular and overall mortality for patients with kidney failure. Although kidney transplantation represents the most effective therapeutic option, it is not devoid of the risk of failure. Immunological and non-immunological risk factors are involved. These factors often interact and may act synergistically, ultimately influencing graft longevity and patient survival. Both contribute to long-term transplant outcomes; however, non-immunological factors, representing a significant clinical challenge, will be the focus of our review. Of the numerous non-immunological risk factors, for clarity and to avoid overextending the discussion, only those most closely associated with chronic kidney disease have been considered: hypertension, anemia, diabetes mellitus, proteinuria, electrolyte and acid–base imbalances, and impaired bone mineralization. Hypertension is reported in approximately 90% of kidney transplant recipients, often related to immunosuppressive therapy and residual renal dysfunction, and it is strongly associated with reduced graft survival. Anemia affects approximately 20–51% of these patients, contributing to cardiovascular morbidity and a more rapid decline in graft function, as does pre-existing diabetes mellitus. Proteinuria has a prevalence ranging from 7.5% to 45%, depending on the established target, and is a significant negative prognostic factor. Metabolic complications are also frequent; for example, hyperkalemia has an incidence of 25–44%, and metabolic acidosis has a prevalence of 12–58%. In our review, each of these factors is analyzed in terms of clinical impact, etiopathogenic mechanism, and available therapeutic management.

## Linked entities

- **Diseases:** chronic kidney disease (MONDO:0005300), anemia (MONDO:0002280), diabetes mellitus (MONDO:0005015), proteinuria (MONDO:0003634), metabolic acidosis (MONDO:0000440)

## Full-text entities

- **Genes:** EDN1 (endothelin 1) [NCBI Gene 1906] {aka ARCND3, ET1, HDLCQ7, PPET1, QME}, PTH (parathyroid hormone) [NCBI Gene 5741] {aka FIH1, PTH1}, FGF23 (fibroblast growth factor 23) [NCBI Gene 8074] {aka ADHR, FGFN, HFTC2, HPDR2, HYPF, PHPTC}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, GIP (gastric inhibitory polypeptide) [NCBI Gene 2695], TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, ABCC2 (ATP binding cassette subfamily C member 2) [NCBI Gene 1244] {aka ABC30, CMOAT, DJS, MRP2, cMRP}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, APOL1 (apolipoprotein L1) [NCBI Gene 8542] {aka APO-L, APOL, APOL-I, FSGS4}, ABCB1 (ATP binding cassette subfamily B member 1) [NCBI Gene 5243] {aka ABC20, CD243, CLCS, ENPAT, GP170, MDR1}, EPO (erythropoietin) [NCBI Gene 2056] {aka DBAL, ECYT5, EP, MVCD2}, HAMP (hepcidin antimicrobial peptide) [NCBI Gene 57817] {aka HEPC, HFE2B, LEAP1, PLTR}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, PAX5 (paired box 5) [NCBI Gene 5079] {aka ALL3, BSAP, PAX-5}, SLC34A1 (solute carrier family 34 member 1) [NCBI Gene 6569] {aka FRTS2, HCINF2, NAPI-3, NPHLOP1, NPT2, NPTIIa}, CYP3A5 (cytochrome P450 family 3 subfamily A member 5) [NCBI Gene 1577] {aka CP35, CYPIIIA5, P450PCN3, PCN3}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, SLC12A3 (solute carrier family 12 member 3) [NCBI Gene 6559] {aka NCC, NCCT, TSC}, DPP4 (dipeptidyl peptidase 4) [NCBI Gene 1803] {aka ADABP, ADCP2, CD26, DPPIV, TP103}, AGTR1 (angiotensin II receptor type 1) [NCBI Gene 185] {aka AG2S, AGTR1B, AT1, AT1AR, AT1B, AT1BR}, AGT (angiotensinogen) [NCBI Gene 183] {aka ANHU, SERPINA8, hFLT1}
- **Diseases:** stroke (MESH:D020521), chronic diarrhea (MESH:D003967), AKI (MESH:D058186), Vitamin D Deficiency (MESH:D014808), hyperkalemic (OMIM:614495), vascular complications (MESH:D003925), adenomas (MESH:D000236), volume depletion (MESH:C536350), focal segmental glomerulosclerosis (MESH:D005923), arrhythmias (MESH:D001145), cytomegalovirus infection (MESH:D003586), skin cancers (MESH:D012878), obesity (MESH:D009765), bone and mineral metabolism disorders (MESH:D001851), Iron deficiency (MESH:D000090463), hypoxia (MESH:D000860), bone demineralization (MESH:D018488), renal masses (MESH:C536030), iron deficiency anemia (MESH:D018798), Proteinuria (MESH:D011507), hypoglycemic (MESH:C000721848), kidney function (MESH:D007680), stenosis (MESH:D003251), Ischemia (MESH:D007511), chronic fatigue (MESH:D015673), metabolic disorders (MESH:D008659), convulsive (MESH:D012640), Hypomagnesemia (OMIM:613882), coronary heart disease (MESH:D003327), nephrotic (MESH:D009404), ABMR (MESH:D020274), fracture (MESH:D050723), Hyperkalemia (MESH:D006947), Hyperparathyroidism (MESH:D006961), parathyroid hyperplasia (MESH:D010279), fibrosis (MESH:D005355), peripheral vascular disease (MESH:D016491), hyperglycemia (MESH:D006943), PCP (MESH:D011020), mesangial IgA glomerulonephritis (MESH:D017098), injury (MESH:D014947), inflammation (MESH:D007249), sarcopenia (MESH:D055948), CKD (MESH:D051436), uremic anorexia (MESH:D000855), atrophy (MESH:D001284), secondary hyperparathyroidism (MESH:D006962), hyponatremia (MESH:D007010), hepatitis C (MESH:D019698), blood loss (MESH:D016063), graft dysfunction (MESH:D055031), weakness (MESH:D018908), intestinal dysbiosis (MESH:D064806), endothelial dysfunction (MESH:D014652), genitourinary tract infections (MESH:C564424), osteonecrosis (MESH:D010020), DM (MESH:D003920), malignancies (MESH:D009369), opportunistic infections (MESH:D009894), calcifications (MESH:D002114)
- **Chemicals:** Sulfonylureas (MESH:D013453), iron (MESH:D007501), fludrocortisone (MESH:D005438), Metformin (MESH:D008687), atovaquone (MESH:D053626), Electrolyte (MESH:D004573), dapsone (MESH:D003622), Thiazide (MESH:D049971), nitric oxide (MESH:D009569), vildagliptin (MESH:D000077597), Patiromer (MESH:C568789), calcium phosphate (MESH:C020243), cinacalcet (MESH:D000069449), oxygen (MESH:D010100), Linagliptin (MESH:D000069476), Acid (MESH:D000143), Phosphate (MESH:D010710), salt (MESH:D012492), sodium polystyrene sulfonate (MESH:C003321), Phosphorus (MESH:D010758), saline (MESH:D012965), vitamin D (MESH:D014807), MMF (MESH:D009173), SRL (MESH:D020123), azathioprine (MESH:D001379), Aldosterone (MESH:D000450), prostaglandins (MESH:D011453), sitagliptin (MESH:D000068900), ganciclovir (MESH:D015774), vitamin B12 (MESH:D014805), thromboxane (MESH:D013931), TMP/SMX (MESH:D015662), steroid (MESH:D013256), RAs (MESH:D011883), ATP (MESH:D000255), folic acid (MESH:D005492), finerenone (MESH:C576501), Sodium Zirconium Cyclosilicate (MESH:C000597310), calcium (MESH:D002118), creatinine (MESH:D003404), glucose (MESH:D005947), magnesium (MESH:D008274), Bisphosphonates (MESH:D004164), calcitriol (MESH:D002117), CsA (MESH:D016572), tetracycline (MESH:D013752), Sodium (MESH:D012964), everolimus (MESH:D000068338), Teriparatide (MESH:D019379), denosumab (MESH:D000069448), Tacrolimus (MESH:D016559), potassium (MESH:D011188), prednisolone (MESH:D011239), sodium bicarbonate (MESH:D017693), DPP-4i (-), bicarbonate (MESH:D001639)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

190 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942542/full.md

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Source: https://tomesphere.com/paper/PMC12942542