Targeting Inflammation in Diabetic Kidney Disease: Is There a Role for Pentoxifylline?

被引:11
作者
Leehey, David J. [1 ,2 ]
机构
[1] Vet Affairs Hosp, Hines, IL USA
[2] Loyola Univ Med Ctr, Maywood, IL 60153 USA
来源
KIDNEY360 | 2020年 / 1卷 / 04期
关键词
Diabetes and the Kidney; Anti-Inflammatory Agents; Diabetic Nephropathies; Inflammation; Pentoxifylline; Sodium-Glucose Transporter 2 Inhibitors; Standard of Care; TUMOR-NECROSIS-FACTOR; URINARY ALBUMIN EXCRETION; BARDOXOLONE METHYL; KLOTHO EXPRESSION; OXIDATIVE STRESS; FACTOR-ALPHA; SHORT-TERM; STAGE; TYPE-2; NEPHROPATHY;
D O I
10.34067/KID.0001252019
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Diabetic kidney disease (DKD) is the most common cause of ESKD in the United States and worldwide. Current treatment for DKD includes strict glycemic control and normalization of BP with renin-angiotensin-aldosterone system (RAAS) blockade. Although RAAS blockers slow progression of disease, they do not generally prevent ESKD and none of the studies with these agents in DKD included patients who were nonproteinuric, which make up an increasingly large percentage of patients with diabetes now seen in clinical practice. Recent studies with glucagon-like peptide-1 receptor agonists and sodium-glucose cotransporter-2 (SGLT2) inhibitors have shown beneficial renal effects, and the benefits of SGLT2 inhibitors likely extend to patients who are nonproteinuric. However, there remains a need to develop new therapies for DKD, particularly in those patients with advanced disease. A role of chronic low-grade inflammation in microvascular complications in patients with diabetes has now been widely accepted. Large clinical trials are being carried out with experimental agents such as bardoxolone and selonsertib that target inflammation and oxidative stress. The Food and Drug Administration-approved, nonspecific phosphodiesterase inhibitor pentoxifylline (PTX) has been shown to have anti-inflammatory effects in both animal and human studies by inhibiting the production of proinflammatory cytokines. Small randomized clinical trials and meta-analyses indicate that PTX may have therapeutic benefits in DKD, raising the possibility that a clinically available drug may be able to be repurposed to treat this disease. A large, multicenter, randomized clinical trial to determine whether this agent can decrease time to ESKD or death is currently being conducted, but results will not be available for several years. At this time, the combination of RAAS blockade plus SGLT2 inhibition is considered standard of care for DKD, but it may be reasonable for clinicians to consider addition of PTX in patients whose disease continues to progress despite optimization of current standard-of-care therapies.
引用
收藏
页码:292 / 299
页数:8
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