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Residual microvascular risk in diabetes: unmet needs and future directions
Paola Fioretto1, Paul M Dodson, Dan Ziegler
1Department of Medical and Surgical Sciences, University of Padova, Via Giustiniani 2, 35128 Padova, Italy. paola.fioretto@unipd.it
Abstract:
The burden of microvascular disease in patients with type 2 diabetes mellitus continues to escalate worldwide. Current standards of care reduce but do not eliminate the risk of diabetic retinopathy, nephropathy or neuropathy in these patients. Correction of atherogenic dyslipidemia, which is characterized by elevated triglyceride levels and low levels of HDL cholesterol, might provide additional benefit. Whereas promising data have been published with respect to fibrate therapy for maculopathy, fenofibrate for diabetic retinopathy, and statin or fibrate therapy for diabetic nephropathy, further studies are warranted to define optimal management strategies for reducing the residual microvascular risk. Such strategies are especially relevant in cases of diabetic peripheral neuropathy, where even optimal care fails to affect disease progression. Identification of those factors that are most relevant to residual diabetes-related microvascular risk is a priority of an ongoing multinational epidemiological study. In this Review, we highlight an urgent need to address the issue of microvascular residual risk in patients with or at risk of type 2 diabetes mellitus.
Insights
Patients with type 2 diabetes face escalating microvascular disease risks. Addressing residual risks from dyslipidemia, particularly with fenofibrate and statins, is crucial for preventing complications like retinopathy and neuropathy.
Area of Science:
- Endocrinology and Metabolism
- Cardiovascular Research
- Ophthalmology
Background:
- Type 2 diabetes mellitus (T2DM) is a global health crisis with escalating microvascular disease burden.
- Current treatments for T2DM do not fully eliminate risks of retinopathy, nephropathy, and neuropathy.
- Atherogenic dyslipidemia, marked by high triglycerides and low HDL cholesterol, is a key factor in residual microvascular risk.
Purpose of the Study:
- To review the current understanding of microvascular residual risk in T2DM.
- To highlight the potential benefits of managing dyslipidemia for reducing microvascular complications.
- To emphasize the need for further research into optimal management strategies for residual risk.
Main Methods:
- Review of existing literature on T2DM microvascular complications.
- Analysis of studies investigating lipid-modifying therapies (fibrates, statins) for diabetic complications.
- Discussion of ongoing epidemiological studies to identify risk factors.
Main Results:
- Promising data exist for fibrate therapy in diabetic maculopathy and retinopathy.
- Statin or fibrate therapy shows potential for diabetic nephropathy.
- Optimal care currently fails to halt progression in diabetic peripheral neuropathy, underscoring residual risk.
Conclusions:
- Managing atherogenic dyslipidemia may offer additional benefits beyond glucose control in T2DM.
- Further studies are essential to define optimal strategies for mitigating residual microvascular risk.
- Addressing residual risk is a priority, especially for diabetic peripheral neuropathy.
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