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“When my son was diagnosed [with Type 1], I knew nothing about diabetes. I changed my research focus, thinking, as any parent would, ‘What am I going to do about this?’” says Douglas Melton.

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Breakthrough within reach for diabetes scientist and patients nearest to his heart

Harvard Correspondent

100 years after discovery of insulin, replacement therapy represents ‘a new kind of medicine,’ says Stem Cell Institute co-director Douglas Melton, whose children inspired his research

When Vertex Pharmaceuticals announced last month that its investigational stem-cell-derived replacement therapy was, in conjunction with immunosuppressive therapy, helping the first patient in a Phase 1/2 clinical trial robustly reproduce his or her own fully differentiated pancreatic islet cells, the cells that produce insulin, the news was hailed as a potential breakthrough for the treatment of Type 1 diabetes. For Harvard Stem Cell Institute Co-Director and Xander University Professor Douglas Melton, whose lab pioneered the science behind the therapy, the trial marked the most recent turning point in a decades-long effort to understand and treat the disease. In a conversation with the Gazette, Melton discussed the science behind the advance, the challenges ahead, and the personal side of his research. The interview was edited for clarity and length.

Douglas Melton

GAZETTE: What is the significance of the Vertex trial?

MELTON: The first major change in the treatment of Type 1 diabetes was probably the discovery of insulin in 1920. Now it’s 100 years later and if this works, it’s going to change the medical treatment for people with diabetes. Instead of injecting insulin, patients will get cells that will be their own insulin factories. It’s a new kind of medicine.

GAZETTE: Would you walk us through the approach?

MELTON: Nearly two decades ago we had the idea that we could use embryonic stem cells to make functional pancreatic islets for diabetics. When we first started, we had to try to figure out how the islets in a person’s pancreas replenished. Blood, for example, is replenished routinely by a blood stem cell. So, if you go give blood at a blood drive, your body makes more blood. But we showed in mice that that is not true for the pancreatic islets. Once they’re removed or killed, the adult body has no capacity to make new ones.

So the first important “a-ha” moment was to demonstrate that there was no capacity in an adult to make new islets. That moved us to another source of new material: stem cells. The next important thing, after we overcame the political issues surrounding the use of embryonic stem cells, was to ask: Can we direct the differentiation of stem cells and make them become beta cells? That problem took much longer than I expected — I told my wife it would take five years, but it took closer to 15. The project benefited enormously from undergraduates, graduate students, and postdocs. None of them were here for 15 years of course, but they all worked on different steps.

GAZETTE: What role did the Harvard Stem Cell Institute play?

MELTON: This work absolutely could not have been done using conventional support from the National Institutes of Health. First of all, NIH grants came with severe restrictions and secondly, a long-term project like this doesn’t easily map to the initial grant support they give for a one- to three-year project. I am forever grateful and feel fortunate to have been at a private institution where philanthropy, through the HSCI, wasn’t just helpful, it made all the difference.

I am exceptionally grateful as well to former Harvard President Larry Summers and Steve Hyman, director of the Stanley Center for Psychiatric Research at the Broad Institute, who supported the creation of the HSCI, which was formed specifically with the idea to explore the potential of pluripotency stem cells for discovering questions about how development works, how cells are made in our body, and hopefully for finding new treatments or cures for disease. This may be one of the first examples where it’s come to fruition. At the time, the use of embryonic stem cells was quite controversial, and Steve and Larry said that this was precisely the kind of science they wanted to support.

GAZETTE: You were fundamental in starting the Department of Stem Cell and Regenerative Biology. Can you tell us about that?

MELTON: David Scadden and I helped start the department, which lives in two Schools: Harvard Medical School and the Faculty of Arts and Science. This speaks to the unusual formation and intention of the department. I’ve talked a lot about diabetes and islets, but think about all the other tissues and diseases that people suffer from. There are faculty and students in the department working on the heart, nerves, muscle, brain, and other tissues — on all aspects of how the development of a cell and a tissue affects who we are and the course of disease. The department is an exciting one because it’s exploring experimental questions such as: How do you regenerate a limb? The department was founded with the idea that not only should you ask and answer questions about nature, but that one can do so with the intention that the results lead to new treatments for disease. It is a kind of applied biology department.

GAZETTE: This pancreatic islet work was patented by Harvard and then licensed to your biotech company, Semma, which was acquired by Vertex. Can you explain how this reflects your personal connection to the research?

MELTON: Semma is named for my two children, Sam and Emma. Both are now adults, and both have Type 1 diabetes. My son was 6 months old when he was diagnosed. And that’s when I changed my research plan. And my daughter, who’s four years older than my son, became diabetic about 10 years later, when she was 14.

When my son was diagnosed, I knew nothing about diabetes and had been working on how frogs develop. I changed my research focus, thinking, as any parent would, “What am I going to do about this?” Again, I come back to the flexibility of Harvard. Nobody said, “Why are you changing your research plan?”

GAZETTE: What’s next?

MELTON: The stem-cell-derived replacement therapy cells that have been put into this first patient were provided with a class of drugs called immunosuppressants, which depress the patient’s immune system. They have to do this because these cells were not taken from that patient, and so they are not recognized as “self.” Without immunosuppressants, they would be rejected. We want to find a way to make cells by genetic engineering that are not recognized as foreign.

I think this is a solvable problem. Why? When a woman has a baby, that baby has two sets of genes. It has genes from the egg, from the mother, which would be recognized as “self,” but it also has genes from the father, which would be “non-self.” Why does the mother’s body not reject the fetus? If we can figure that out, it will help inform our thinking about what genes to change in our stem cell-derived islets so that they could go into any person. This would be relevant not just to diabetes, but to any cells you wanted to transplant for liver or even heart transplants. It could mean no longer having to worry about immunosuppression.

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New insights into diabetes mellitus and its complications: a narrative review

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Correspondence to: Prof. Fei Hua, MD, PhD. Department of Endocrinology, the Third Affiliated Hospital of Soochow University, Changzhou, China. Email: [email protected] .

Corresponding author.

Received 2020 Aug 6; Accepted 2020 Dec 16; Issue date 2020 Dec.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 .

Diabetes is a metabolic disorder accompanied by complications of multiple organs and systems. Diabetic nephropathy (DN) is one of the most prevalent lethal complications of diabetes. Although numerous biomarkers have be clarified for early diagnosis of DN, renal biopsy is still the gold standard. As a noninvasive imaging diagnostic method, blood oxygen level-dependent (BOLD) MRI can help understand the kidney oxygenation status and fibrosis process and monitor the efficacy of new drugs for DN via monitoring renal blood oxygen levels. Recent studies have shown that noncoding RNAs including microRNAs (miRNAs), long noncoding RNAs (lncRNAs) and circular RNAs (circRNAs) were all involved in the development of DN, which could be exploited as therapeutic strategy to control DN. Dyslipidemia is also a common complication of diabetes. Apolipoprotein M (apoM), as a novel apolipoprotein, may be related to the development and progression of diabetes, which need to further investigation. Obstructive sleep apnea (OSA) is another common complication of diabetes and is an independent risk factor for cardiovascular disease (CVD). At present, there is no simple, effective and rapid diagnostic method to early identification of OSA in patients with diabetes. A nomogram consisted of waist-to-hip ratio, smoking status, body mass index, serum uric acid, HOMA-IR and history of fatty liver might be an alternative method to early assess the risk of OSA.

Keywords: Diabetes mellitus (DM), diabetic nephropathy (DN), dyslipidemia, apolipoprotein M (apoM), obstructive sleep apnea (OSA)

Introduction

Diabetes mellitus (DM), as a growing epidemic of bipolar disorder, affects near 5.6% of the world’s population ( 1 ). Its global prevalence was about 8% in 2011 and is predicted to rise to 10% by 2030 ( 2 ). Likewise, its prevalence in China also increased rapidly from 0.67% in 1980 to 10.4% in 2013 ( 3 ). Therefore, DM is a contributing factor to morbidity and mortality. So far, various organizations have developed various diabetic guidelines to clarify the definition, classification, diagnosis, screening, and prevention of this disease, which are used not for clinical management but also the monitoring of ongoing care with laboratory check-ups at regular intervals, lifestyle counseling, and prevention of diabetic-related complications.

The diagnostic criteria for DM are based primarily on fasting plasma glucose (FPG), random plasma glucose or oral glucose tolerance test (OGTT) 2-hour plasma glucose (2hPG). In 2011, WHO recommended wherever conditions permit, countries and regions may consider adopting the hemoglobin A1c (HbA1c) ≥6.5% as the cut-point for a diabetes diagnosis. Several studies have shown that the optimal cut-off value for HbA1c to diagnose diabetes in Chinese adults is 6.3%. However, HbA1c has not yet been included in the latest guidelines for diabetes in China ( 3 ).

DM is classified into four types: type 1 diabetes mellitus (T1DM), T2DM, other specific types of diabetes, and gestational diabetes mellitus (GDM), whereas T2DM is the most common form and occurs when the target tissue (the liver, skeletal muscles, and adipose tissues) loses insulin sensitivity. In the United States, the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD) guidelines, and the American Association of Clinical Endocrinologists (AACE) and the American College of Endocrinology (ACE) guidelines are two typically consulted to determine optimal therapeutic decisions in patients with T2DM. The differences between the two guidelines are: (I) the ADA/EASD guideline advocates a stepwise approach to glycemic control, starting with metformin and incrementally intensifying to dual and triple therapy at 3-month intervals until the patient is at their individualized goal, whereas the AACE/ACE guideline provides a broader choice of first-line medications, with a suggested hierarchy of use. It encourages initial dual and triple therapy if the HbA1c level is 7.59.0% and >9.0% at diagnosis, respectively. (II) Compared with the value in the AACE/ACE guideline, the target HbA1c value is higher in the ADA/EASD guideline (≤6.5% vs . ≤7.0%) ( 4 ). Considering the ethnic characteristics, social culture, and social resources, the Chinese Diabetes Society (CDS) has drawn up the latest version of guidelines for the prevention and care of T2DM in China in 2019, which may work best for the Chinese patient population. This guideline recommends the target HbA1c value, which is <7% for most nonpregnant adults with T2DM, and drug therapy should be started when HbA1c value is ≥7.0%. Metformin, α-glucosidase inhibitors, or insulin secretagogues could be options for monotherapy. If monotherapy is insufficient, dual and triple therapy or multiple daily insulin injections may be prescribed ( 3 ). Diabetes is a complicated disease that affects multiple organs, requiring multiple treatments and preventive strategies to prevent long-term complications associated with it. The following is a brief narrative review of the diagnosis, prevention and treatment of diabetic complications. MEDLINE was searched using the terms “diabetic nephropathy”, “diabetes and dyslipidemia”, “Apolipoprotein M”, “diabetes and obstructive sleep apnea” for nearly five years.

We present the following article in accordance with the Narrative Review reporting checklist (available at http://dx.doi.org/10.21037/atm-20-7243 ).

Diabetic nephropathy (DN)

DN, as one of the most prevalent lethal complications of diabetes, is observed in approximately 20% to 30% of T2DM individuals ( 5 ). The etiology of DN is multi-factor and involves many molecular signaling pathway abnormalities, including the advanced glycation end products/receptors for AGE (AGE/RAGE), protein kinase C (PKC), reactive oxygen species (ROS), mammalian target of rapamycin (mTOR), Janus Kinase/Signal Transducer and Activator of Transcription Proteins (JAK/STAT), etc. ( 6 ). Chronic hypoxia is one feature of DN. At present, the clinical diagnosis of DN mainly depends on the elevated urinary albumin excretion and reduced eGFR in the absence of other primary causes of kidney damage, lacking high sensitivity and specificity indicators to reflect the renal blood oxygen levels. A growing number of studies have focused on the biomarkers for early diagnosis of DN, which include (I) certain urinary microRNAs such as microRNA-210 and microRNA-34a ( 7 ), urinary kidney injury molecule 1 (KIM-1) and Chitinase-3-like protein 1 (YKL-40) ( 8 ), urinary E-cadherin ( 9 ); (II) serum galectin-3 and growth differentiation factor-15 (GDF-15) ( 10 ), serum pregnenolone sulfate, ganglioside GA1, phosphatidyl glycerol and all-trans-Carophyll yellow tested by direct flow through mass spectrometry ( 11 ); (III) suppressor of mothers against decapentaplegic type 1 (SMAD1) and neutrophil gelatinase-associated lipocalin (NGAL) gene expression in peripheral blood and urine samples ( 12 ). However, renal biopsy is still the gold standard to diagnose diabetic nephropathy. Tong et al. have searched identified 40 studies worldwide between 1977 and 2019 that looked at global renal biopsy and pathological nondiabetic kidney disease (NDKD) lesions. The results have shown that overall prevalence rate of DN, NDKD and DN plus NDKD is 41.3, 40.6 and 18.1%, respectively ( 13 ). Therefore, it is of great significance to do renal biopsy as early as possible to confirm the diagnosis and to enable personalized treatment especially when T2DM patients present atypical diabetic kidney disease (DKD) symptoms (e.g., absence of diabetic retinopathy, shorter duration of diabetes, microscopic hematuria, subnephrotic range proteinuria, lower glycated hemoglobin, lower fasting blood glucose). Ding et al. have shown that texture analysis with DWI, BOLD, and susceptibility-weighted imaging (SWI) can help assess renal dysfunction during the early stages of chronic kidney disease ( 14 ). Jiang et al. reported the role of SWI parameters and SWI-based texture features in evaluating renal dysfunction of T2DM ( 15 ). They showed that the signal intensity ratio of the medulla to psoas muscle (MPswi) was significantly lower than the signal intensity ratio of the cortex to psoas muscle (CPswi) in non-moderate-severe renal injured (non-msRI) group and msRI group. MPswi was higher, whereas the signal intensity ratio of the cortex to the medulla (CMswi), skewness, the correlation was lower in the msRI group than in non-msRI group and CMswi was an independent protective factor for msRI. These results supply a crucial noninvasive method to monitor renal blood oxygen levels, which can help understand the kidney oxygenation status and fibrosis process and monitor the efficacy of new drugs for DN. As a noninvasive imaging diagnostic method, MRI provides some level of spatial resolution and it can be performed repeatedly, providing some level of temporal resolution. Moreover, it is noninvasive and thus can be applied to both animals used in experiments and humans, providing a pathway for translation of new therapies. So far, blood oxygen level–dependent (BOLD) MRI, diffusion tensor imaging (DTI) MRI and dynamic nuclear polarization (DNP) MRI have been confirmed to be used for early identification of DN. A major advantage of BOLD-MRI is that it does not require an exogenous paramagnetic agent, because it relies on the differing paramagnetic properties of oxyhemoglobin and deoxyhemoglobin. BOLD imaging detected the medullary hypoxia at the simply diabetic stage, while DTI didn’t identify the medullary directional diffusion changes at this stage. Therefore, BOLD imaging may be more sensitive for assessment of the early renal function changes than DTI ( 16 ). Furthermore, BOLD-MRI, coupled with other imaging modalities that provide information about renal hemodynamics and function, has provided important insights into the temporal and spatial relationships between renal hypoxia and progression of diabetic nephropathy ( 17 ). However, there are several disadvantages of BOLD-MRI. First, BOLD-MRI provides a measure of blood oxygenation rather than tissue oxygenation. Second, it is not quantitative in the sense that it cannot provide an actual level of PO 2 or even of blood hemoglobin saturation. Third, it is susceptible to artefacts caused by changes in renal blood volume and hemoglobin concentration. DNP-MRI combined with the oxygen-sensitive paramagnetic agent OX63 ( 18 ) is a method for quantifying tissue oxygen tension within the kidney. Nevertheless, this method needs to use an exogenous paramagnetic agent that must be administered intravenously and OX63 is also rather expensive. Therefore, it is used only in small animals such as the mice. Furthermore, either general anesthesia or physical restraint is required during imaging.

Although several clinical approaches are available to relieve symptoms temporarily or impede the progression of DN, there is no curative treatment to date. Therefore, a novel therapeutic strategy is warranted to control DN. MicroRNAs (miRNAs) are a class of non-coding RNAs that can bind to their target mRNAs to take part in the epigenetic machinery of their downstream signaling molecules. Over the past few decades, a plethora of studies has revealed the potential involvement of different miRNAs in different molecular and signaling pathways leading to DN. Several reviews and studies have shown in-depth the vital role of various miRNAs in progression, diagnosis, and therapeutics of DN ( 19 ). Concretely speaking, several miRNAs including miR-21, miR-124, miR-135a, miR-192, miR-195, miR-200, miR-215, miR-216a, miR-217, miR-377, and miR-1207-5p, are overexpressed in DN, whereas some miRNAs (Let-7, miR-25, miR-29, miR-93, miR-141, miR-200, and miR-451) are down-regulated ( 20 ). The roles of miRNAs are multifaceted, involved in the TGF-β signaling pathway, in the PI3K/Akt signaling pathway, in collagen gene expression, in DNA methyltransferases (DNMTs) and histone deacetylases (HDACs), in epithelial-to-mesenchymal transition (EMT) and endothelial-mesenchymal transition (EndMT) and so on ( 20 ). Therefore, both up- and down-regulation of DN-suppressing and DN-promoting miRNAs can be exploited as therapeutic interventions in DN, respectively. Pharmacological inhibition of miRNAs can be achieved through employing miRNA inhibitors, anti-miRNA oligonucleotides (AMOs) and miRNA sponges, while up-regulation of miRNAs can be accomplished using miRNA mimics, miRNA-containing exosomes and miRNA promoters ( 20 ).

Except for the microRNAs (miRNAs), long noncoding RNAs (lncRNAs) and circular RNAs (circRNAs) are also play an important role in DN progression. Several lncRNAs such as the Plasmacytoma Variant Translocation-1 (PVT1) LncRNA, the Nuclear Enriched Abundant Transcript-1 (NEAT1) LncRNA, LncRNA ERBB4-IR, LncRNA CYP4B1-PS1-001 and LncRNA ENSMUST00000147869 are involved in the regulation of renal hypertrophy and extracellular matrix (ECM) accumulation. A few lncRNAs such as LncRNA GM4419, the Metastasis-associated lung adenocarcinoma transcript-1 (MALAT-1) LncRNA, LncRNA GM6135, myocardial infarction-associated transcript (MIAT) LncRNA can regulate renal inflammation and oxidative stress. Furthermore, LncRNA GM5524, LncRNA GAS5, LncRNA GM15645, the Taurine upregulated-1 (TUG-1) LncRNA and the Cancer susceptibility candidate 2 (CASC2) LncRNA are involved in the renal autophagy and apoptosis ( 21 ). The evidence to elucidate the interaction of circular RNA in DN progression is limited. Only one study in DN mice showed that circRNA_15698 expression could regulate the fibrosis of mesangial cells ( 22 ).

Connexins (Cxs) are a multigenic family of transmembrane proteins that form gap junction membrane channels and take part in the exchange of information between adjacent cells. Cx43 is the most abundantly expressed and widely distributed gap junction protein. A previous study has shown that the expression of Cx43 was significantly decreased in DN patients and diabetic model animals ( 23 ). Other studies have shown that the upregulation of Cx43 was involved in podocyte injury, and the interdependence of Cx43 and impaired autophagic flux may be a novel mechanism of podocyte injury in DN ( 24 , 25 ). Also, one latest research has shown the essential role of Cx43 in regulating renal EMT and diabetic renal tubulointerstitial fibrosis via regulating the SIRT1-HIF-1α signaling pathway and provided an experimental basis for Cx43 as a potential target for DN ( 26 ).

Li et al. put forward a new viewpoint that there was a link between miRNA-30 and Cx43 in the podocyte under high glucose ambiance (HG) or diabetic state ( 27 ). They used streptozotocin (STZ)-induced rat model of diabetes and podocyte culture under HG. Both the podocytes and rats were concomitantly treated with miRNA-30 mimic or miRNA-30 inhibitors. The results showed that the expression of miRNA-30 was down-regulated, and the transfection of miRNA-30 reduced podocyte injury, apoptosis, and ERS, both in vivo and in vitro. Luciferase reporter assays confirmed Cx43 is a directed target of microRNA-30s. Likewise, Cx43 siRNA treatment yielded comparable results. From these results, the authors concluded that the overexpression of miRNA-30 prevents DN-induced podocyte damage by modulating Cx43 expression. This study provides novel information that highlights the microRNA-30/Cx43/ERS axis, plays a role in the pathogenesis of DN, and it may serve as a potential therapeutic target for the amelioration of DN. However, considerable research is needed for a better understanding of the regulation and functions of this signaling pathway in DN.

Diabetes and dyslipidemia

Glucose intolerance, dyslipidemia, combined with abdominal obesity and hypertension, together constitute the metabolic syndrome (MetS), which results in a significant increase in morbidity and all-cause mortality. A 10-year prospective study has shown that MetS could lead to 1.80 and 2.05 times higher statistically significant probability for myocardial infarction (MI) and stroke events, respectively. Further studies have shown that abdominal obesity increases the risk of MI, and low levels of high-density lipoprotein cholesterol (HDL-C) and hypertriglyceridemia increase the risk of stroke in men with MetS ( 28 ). Dyslipidemia in adolescence is usually associated with one or more components of the MetS, namely obesity, hypertension, and impaired glucose tolerance, and presents with high triglyceride and low HDL-C. In one trial of adolescents with T2DM, 21% had high triglyceride levels or had been treated with lipid-lowering drugs at baseline, and 23% had high triglyceride (TG) levels three years later ( 29 ). It is worth noting that there is increasing evidence linking T2DM to atherosclerosis, which may attribute to local activation of the RAS and its components, including receptors and relevant enzymes in the microvessel ( 30 ). Also, high TG, low HDL-C, increased LDL particle number or apolipoprotein B, smaller LDL size and density, and LDL glycation and oxidation are all associated with increased atherosclerosis ( 31 ). The EVAPORATE trial has revealed HDL-C levels are negatively correlated with baseline coronary plaque, total plaque (TP), and total non-calcified plaque (TNCP) volumes, providing more detailed mechanistic evidence for the protective effect of HDL-C on coronary atherosclerosis in high-risk populations ( 32 ). China’s latest guideline has recommended that the therapeutic targets for lipids are: LDL-C <2.60 mmol/L, TG <1.70 mmol/L, HDL-C ≥1.0 mmol/L, to prevent clinical cardiovascular disease (CVD) ( 3 ). Therefore, treatment measures should be taken when LDL-C, TG, and HDL-C levels exceed cut points in diabetic patients.

Apolipoprotein M (apoM) is a novel apolipoprotein bound primarily to HDL in plasma. Many previous studies have shown that in diabetic mouse models, the expression of apoM in plasma, liver, and kidney is all remarkably decreased, which may be attributed to the decreased expression of peroxisome proliferator-activated receptor and liver X receptor secondary to hyperglycemia ( 33 , 34 ). However, the results of studies on apoM expression in diabetic patients are inconsistent. Several studies have shown that plasma apoM levels decreased significantly in maturity-onset diabetes of the young 3 (MODY3) individuals with HNF-1 mutation, whereas these levels remained unchanged in MODY1 patients ( 35 ). Contradicting results have been reported no significant differences in apoM concentrations among MODY3, T2DM, and healthy individuals ( 36 ). The inconsistency between studies may apply to differences in methods (e.g., dot blot, immunoblot, and ELISA) used to detect serum apoM. Also, previous studies have determined apoM levels were negatively correlated with the development and progression of diabetes, which could be attributed to Sphingosine-1-Phosphate, a functional lipid that can promote β-cell functions, and insulin secretion and improve glucose tolerance ( 37 , 38 ). Finally, genetic variations in the apoM gene have also played a prominent role in diabetes susceptibility. Wu et al. found that SNP T-778C was strongly associated with T1DM in both Han Chinese and Swedish populations, and allele C of SNP T-778C may increase promoter activity and confer the risk susceptibility to the development of T1DM ( 39 ). More recently, a study by Liu et al. suggested that rs805296 (T-778C)-C and rs9404941 (T-855C)-C alleles haplotypes were indicators of high T2DM risk ( 40 ). However, another study drew a different conclusion that there was no association between the apoM gene and T2DM susceptibility in Hong Kong Chinese cohort. Interestingly, the C allele of rs805297 was significantly associated with T2DM duration of longer than ten years ( 41 ). Therefore, the relationship between apoM and diabetes deserves further investigation.

According to the study by Yao et al. ( 42 ), apoM is expressed on all peripheral blood mononuclear cells (PBMCs). Impressively, compared with the other monocytes, CD14 + cells, the central immune cells, in the atherosclerotic process, have the highest rates of apoM+ cells, suggesting that apoM might take part in the pathological lesions of atherosclerosis. The investigators found both apoM + HDL and apoM – HDL could downregulate the expression of IL-6, IL-1β, and MCP-1 in macrophages, and the downregulation of TNF-α, IL-6, and IL-1β was more significant in the apoM + HDL group than in the apoM – HDL group. Notably, the expression of IL-10, an anti-inflammatory cytokine preventing lipid deposition and inflammation in atherosclerotic lesions, was significantly upregulated in the apoM + HDL group. In this study, the investigators used coimmunoprecipitation to detect the binding of purified apoM + HDL and apoM – HDL proteins to SR-BI, the physiological receptor for apoA-I/HDL which was expressed on the surface of THP-1 macrophages. The results showed that the recombinant human apoM, human apoM – HDL, and human apoM + HDL particles could interact with SR-BI, highlighting that apoM could promote the anti-inflammatory effects of HDL, possibly by binding to SR-BI. However, further studies are necessary to investigate the downstream signaling pathway.

Diabetes and obstructive sleep apnea (OSA)

OSA is characterized by recurrent partial (hypopnea) or complete (apnea) upper airway obstruction, leading to hypoxia, recurrent arousal from sleep, and desaturation-reoxygenation sequences ( 43 ). Data from previous research suggest OSA is associated with many metabolic abnormalities, including impaired fatty acid handling, glucose tolerance, and insulin sensitivity, atherogenesis, and high blood pressure, through the effects of sleep fragmentation, intermittent hypoxia, sympathetic overactivity, and adipose tissue inflammation ( 43 , 44 ). Also, many studies have confirmed that OSA is an independent risk factor for CVD ( 45 ). Notably, a recent study showed that OSA could cause a significant increase in all-cause mortality and major adverse cardiac events (MACEs) in patients with T2DM and co-existing OSA following percutaneous coronary intervention (PCI) ( 46 ).The investigators proposed several mechanisms by which OSA contributes to cardiovascular events, including endothelial dysfunction, vascular inflammation, and high platelet reactions resulting from intermittent hypoxemia, autonomic imbalance, and sleep disruption ( 47 ). Therefore, early diagnosis and management of OSA might be critical for patients with T2DM to reduce the risk of MACEs.

A study by Shi et al. ( 48 ) constructed and validated an easy-to-use nomogram comprising six items, namely waist-to-hip ratio, smoking status, body mass index, serum uric acid, HOMA-IR and history of fatty liver which could accurately predict and rapidly assess the risk of OSA in patients with T2DM, and help identify patients at high risk of OSA that should be referred for diagnostic polysomnography. This nomogram, as a lesscostly and time-consuming examination, is worthy of clinical promotion to reduce the number of missed OSA diagnoses in patients with T2DM. However, the sensitivity and specificity of this nomogram need further evaluation in the general population.

Conclusions

Diabetes is a metabolic disorder that has resulted in critical personal health hazards and public severe health burdens worldwide, often accompanied by chronic systemic complications in multiple organs and systems, including diabetic nephropathy, diabetic retinopathy, diabetic neuropathy, and so on. Moreover, diabetes is associated with metabolic syndrome and OSA. Simple and easy detection methods with high sensitivity are conducive to the early diagnosis of diabetic complications. Clarifying the mechanism of diabetic complications is conducive to develop new drugs and therapies.

Supplementary

The article’s supplementary files as

Acknowledgments

Funding: None

Ethical Statement: The author is accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Reporting Checklist: The author was completed the Narrative Review reporting checklist. Available at http://dx.doi.org/10.21037/atm-20-7243

Conflicts of Interest: The author has completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/atm-20-7243 ). The author has no conflicts of interest to declare.

(English Language Editor: J. Chapnick)

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Clinical Trials

A clinical trial is a way to carefully test a new drug or device in patients before it is approved by the FDA to be used in the general public. Clinical trials are an important step in our being able to have new treatments for diabetes and other conditions.

The American Diabetes Association is currently a partner providing support for the following clinical studies and initiatives:

TrialNet Type 1 Diabetes TrialNet is an international network of researchers who are exploring ways to prevent, delay and reverse the progression of type 1 diabetes.

GRADE GRADE is a comparative effectiveness study looking at what medications work best at lowering blood sugar levels in patients who are newly diagnosed with diabetes.

RISE The Restoring Insulin Secretion study (RISE) includes 3 studies examining whether aggressive glucose lowering will lead to recovery of pancreas function in those with prediabetes and early type 2 diabetes.

D2d The goal of the Vitamin D and type 2 diabetes (D2d) study is to determine whether vitamin D supplementation is safe and effective in delaying the onset of type 2 diabetes in people at risk for the disease, and to gain a better understanding of how vitamin D affects glucose metabolism.

Accelerating Medicines Partnership The Accelerating Medicines Partnership (AMP) is a bold new venture between the NIH, non-profit organizations and biopharmaceutical companies to transform the current model for developing new diagnostics and treatments. By jointly identifying and validating promising biological targets of disease, the partnership strives to increase the number of new diagnostics and therapies for patients and reduce the time and cost of developing them.

FNIH Biomarkers Consortium The Biomarkers Consortium is a public-private biomedical research partnership managed by the Foundation for the National Institutes of Health that endeavors to discover, develop, and qualify biological markers (biomarkers) to support new drug development, preventive medicine, and medical diagnostics.

Clinical trials links and resources

By policy, the American Diabetes Association does not list or promote specific clinical trials other than the trials above in which it is a formal collaborator. This policy also applies to patient surveys. There are far too many trials and surveys being conducted at any given time for the Association to be able to evaluate them on an individual basis. However, the following resources from the Food and Drug Administration and the National Institutes of Health provide more information about clinical trials and how to determine which trials are being conducted in a location near you.

ClinicalTrials.gov A registry and results database of federally and privately supported clinical trials conducted in the United States and around the world. ClinicalTrials.gov gives you information about a trial's purpose, who may participate, locations and phone numbers for more details.

National Institutes of Health (NIH) The National Institutes of Health (NIH), a part of the U.S. Department of Health and Human Services, is the nation's medical research agency—making important discoveries that improve health and save lives.

Food and Drug Administration (FDA) FDA is responsible for protecting the public health by assuring the safety, efficacy and security of human and veterinary drugs, biological products, medical devices, our nation's food supply, cosmetics, and products that emit radiation.

Centers for Medicare and Medicaid Service: Clinical Trials Coverage (CMS)

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