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Sunday, June 9, 2019

Lower Insulin Demand Associated With Gluten-Free Diet in Recent-Onset T1D

A gluten-free diet was associated with lower insulin demand and lower glycated hemoglobin (HbA1c) in newly diagnosed nonceliac pediatric patients with type 1 diabetes(T1D), according to study results presented at the American Diabetes Association 79th Scientific Sessions, held June 7 to 11, 2019, in San Francisco, California.
Researchers aimed to test whether a gluten-free diet could decelerate the decline in beta-cell capacity in newly diagnosed nonceliac pediatric patients with T1D. The nonrandomized self-selected intervention trial enrolled 46 pediatric patients, age 10.2 ± 3.3 years. Of the total patients enrolled, 26 started with a gluten-free diet and 20 were kept on a standard diet.
Researchers looked for a decline in C-peptide area under the curve in mixed-meal tolerance tests, as well as the differences in insulin dose, insulin dose-adjusted A1c, and HbA1c over a 12-month period. Adherence to a gluten-free diet was tested by immunoreactive gluten in patient stool samples and further data was analyzed as intention-to-treat by linear regression models.

Results showed a mean decrease in C-peptide area under the curve, with 293 vs 484 pmol/L (P =.3) at 6 months and 567 vs 919 pmol/L (P =.10) at 12 months in the gluten-free diet and standard diet groups, respectively. The gluten-free diet group showed lower insulin dose by 0.22 U/kg/d (=.007), lower insulin dose-adjusted A1c by 1.5 (P =.003), and lower mean HbA1c by 7.5 mmol/mol (P =.01) at 12 months.
Immunoreactive gluten was found in the stool of 3 patients and there was no difference in daily carbohydrate intake between the gluten-free diet and standard diet groups (P =.40).

Reference
Neuman V, Pruhova S, Kulich M, et al. Gluten-free diet in children with recent-onset type 1 diabetes without coeliac disease: a 12-month intervention trial. Presented at: American Diabetes Association 79th Scientific Sessions; June 7-11, 2019; San Francisco, CA. Poster 1378-P.

Pfizer: The race to replace Viagra

Are we witnessing the end of an era for Viagra and Pfizer? Since the famous “little blue pill” exploded on to the market in 1998, becoming the fastest selling drug in history, the American pharmaceutical giant has made vast sums marketing it to erectile dysfunction sufferers all over the world. Within three months of its launch, Viagra had already earned Pfizer$400m, and over the past two decades, it has consistently generated annual sales to the tune of $1.8bn.
However, this will soon come to an end, as in 2020, Pfizer’s remaining patents on Viagra expire for good. A whole host of generic versions have emerged in the past six years, often in quirky forms such as mint strips or breath sprays, as Pfizer’s grip on the rights to the drug has slowly loosened. Soon, these are expected to flood the market, as manufacturers jostle for a slice of the pie.
This will make Viagra more accessible and cheaper, but for the millions of men worldwide with erectile dysfunction, it could also spell good news in the form of much needed treatment innovations. Since Viagra was launched, few genuinely novel therapies have been developed, and while Viagra and similar drugs like Cialis and Levitra – which all increase blood flow to the penis by blocking an enzyme known as PDE5 – are effective in around 70% of patients, they come with significant downsides.
To start with, there are often prominent side-effects ranging from headaches to stomach pain. In addition, with Viagra taking more than an hour to work, there’s the need to pre-plan intercourse, and in the case of older patients, the drugs can often be unsuitable due to potentially dangerous interactions with medications for high blood pressure, or hypertension. For patients with the most severe forms of erectile dysfunction, often resulting from nerve damage due to diabetes or prostate cancer surgery, Viagra typically doesn’t work at all.
The need for better treatments is particularly pressing as erectile dysfunction appears to be getting more common, with the global prevalence set to pass 300 million by the middle of the next decade. Scientists have long argued about whether this is simply due to men becoming more open in reporting their problems, or a by-product of other health problems. One thing is clear: the market is growing.
GTN could potentially be applied directly to the penis as a gel or cream, with near instantaneous results
“There’s a huge need for new treatments which work in the widest patient population possible while having a longer-acting effect to improve spontaneity and reduce the stress of having to take them on a planned basis,” says Dr Samit Soni, a urologist at the Baylor College of Medicine in Houston, Texas. “Many patients would like to be able to take something and then not have to worry about it for 30 days.”
But right now, there are few options. The only alternatives to Viagra consist of medications which need to be injected directly into the shaft of the penis in order to improve blood flow, or complex surgery to fit penis pumps or prosthetic implants. Neither are particularly palatable.
So why is this? While a handful of pharma companies have attempted and failed to get rival drugs into the clinic, the sheer scale of the Viagra profit machine created a monopoly, with most companies shying away from the challenge, perceiving it as too much of a risk. But experts believe this could be about to change.
“For many years after Viagra was developed, little changed in our understanding of erectile dysfunction and how to correct it,” says Soni. “But with the patent expiration there’s definitely a renewed interest in alternative pathways for treating erectile dysfunction, and using them to develop new ideas that can be patented, and provide a sustainable profit to the industry.”
Viagra 2.0
In the early 2000s, scientists at Futura Medical, a pharmaceutical company in Surrey, came across stories of a heart disease medication that appeared to accidentally induce erections.
“There were some anecdotal reports of people deliberately spraying this product on to their penises,” says Ken James, head of research and development at Futura. “These observations had been reported in the scientific literature, and the company thought there might be a commercial opportunity.”
The reported effects were due to a particular molecule known as glyceryl trinitrate or GTN, which causes the dilation of blood vessels in the penis, increasing blood flow. But the reason why Futura were so intrigued was because, while Viagra, Cialis and other drugs have to be taken orally – meaning they reach the target area via the bloodstream and so interact with other systems in the body – GTN could be rapidly absorbed into erectile tissue through the skin. This meant that it could potentially be applied directly as part of a gel or cream, with almost instantaneous results and none of the troublesome side effects associated with Viagra.
“Viagra and Cialis are quite effective drugs but 50% of people stop using them within a year,” says James. “60-70% of people have some degree of dissatisfaction with them. This shows there’s an opportunity if we can come to market with something that addresses many of those concerns.”
Over the past decade, Futura have developed a GTN-based gel called Eroxon which appears to be capable of inducing an erection in patients with mild to moderate erectile dysfunction in five to 10 minutes. Already dubbed the new Viagra by some, it seems to have the potential to be the first genuinely novel treatment for erectile dysfunction in two decades, and Futura have even tentatively placed its potential commercial value at $1bn.
After investors showed a renewed interest in backing novel treatments for erectile dysfunction, Futura completed a clinical trial of 232 patients last year, and have now embarked on a final phase III trial of 1,000 patients to be completed by the end of 2019. If this succeeds, Eroxon could become available clinically within the next couple of years, although urologists remain cautious.
“The biggest question from that phase III trial will be how they compare in clinical efficacy to Viagra,” says Soni. “In the past, we’ve seen that it’s difficult to get similar efficacy with topical administration, but at the same time, our understanding of how drugs can be absorbed through the skin into the bloodstream has massively improved.”
Tackling the most severe cases
But even Futura’s scientists admit that Eroxon is unlikely to help the severest cases of erectile dysfunction, which affect around 20-30% of patients, typically due to nerve damage in the lower abdomen.
In the past there have been few options for these people, but over the past five years, the renewed interest in erectile dysfunction has seen research programmes dedicating more time and money to clinical trials of a technology known as shockwave therapy. Unlike Viagra or Eroxon, this attempts to reverse the problems which cause the dysfunction by passing low-intensity sound waves through erectile tissue.
Desperation has pushed many into private clinics that offer shockwaves, stem cell infusions or injections of plasma
Scientists are still not entirely sure how or why it works, but so far they think it leads to a form of regeneration of the erectile tissue, promoting the growth of new blood vessels and clearing plaque from existing vessels. “Improving the function of these vessels leads to improved blood flow and erections in those patients,” explains Georgios Hatzichristodoulou, who researches shockwave therapy at the University of Würzburg in Germany.
However, because there is such a wide spectrum of causes of erectile dysfunction, shockwave therapy is currently only known to work in a subset of these patients, particularly those where the damage has resulted from diabetes or hypertension.
Hatzichristodoulou points out that there remains a need for further data, with a series of trials of shockwave therapy currently going on in Europe and the US. But compared to Viagra or Eroxon, one of the great promises of the treatment is that it would not be needed on a regular basis. Instead, patients could simply undergo maintenance therapy at half-yearly or annual intervals.
Most tantalisingly, in attempting to restore the natural function of the penis, it points towards an eventual cure, a hope which may yet be realised in years to come.
The search for an all-out cure
Even when Viagra works, one of the problems for people who need to take it indefinitely is that it becomes less effective over the course of months or years.
“This is quite common. Most patients will experience a worsening of their erections after they’ve been on Viagra for a while,” says Hatzichristodoulou. “They take Viagra for five, six, 10 years, and some days they feel that there is little improvement in function.”
Desperation has pushed many patients towards unscrupulous private clinics around the world, who promise an ultimate cure, offering treatments like shockwaves, stem cell infusions and injections of platelet-rich plasma on an unregulated basis. But all of these therapies are highly experimental – as an example, shockwave therapy is currently only approved by the US Food and Drug Administration to stimulate wound healing, as scientists are still working on establishing the best doses for efficacy and investigating long-term safety.
“There’s some particularly compelling data on shockwave therapy, especially in certain patients,” says Soni. “But it is still in an early phase.”
While scientists hope that shockwave therapy may be ready for primetime within the next five to 10 years, progress is also being made on longer-term treatments such as gene therapy which could offer a complete cure. At the Kaiser Permanente Division of Research in northern California, a group of scientists have identified a genetic switch which is thought to be unique to sexual function. They believe that this switch plays a crucial role in controlling the brain signals which initiate an erection, and new genome editing technologies such as Crispr-Cas9 could one day allow scientists to reactivate this switch in patients.
“This genetic location is part of a pathway which is involved in a number of different systems in the body, from pigmentation to weight to sexual function,” explains project leader Eric Jorgenson. “But what is exciting about this, is that it seems to be very specific to sexual function, which would make it possible to target this location and not disturb anything else in the body. But there’s a long way to get there. We need to understand the exact part of the brain where this switch is active, and then try targeting it in mice.”
Because genome editing is still such an experimental concept, Jorgenson says it will take time for regulators to become confident that it could be safe. “The first uses of Crispr-like technology will probably be in patients where there’s more of a direct medical need for experimental therapies,” he says. “You’d need to have a very safe treatment before people will allow it for erectile dysfunction.”
While gene therapy may be a little way off, there are still new treatments on the horizon for erectile dysfunction for the first time in decades. With the Viagra era coming to a close, and increasing amounts of research funding available, the field is in its healthiest state for years.
“There hasn’t been any real innovation in erectile dysfunction for many years now,” says Soni. “These new breakthroughs and treatments are offering excitement to an area of healthcare that has really been lulled for a long time.”

More Severe Complications in Young Adults with Youth-Onset Type 2 Diabetes

By continuing to follow the cohort from the Treatment Options for Type 2 Diabetes in Adolescents and Youth (TODAY) Study sponsored by the National Institutes of Health (NIH), researchers can now report on the extensive development of severe renal, cardiac, eye, nerve, and pregnancy complications in early adulthood in patients with youth-onset type 2 diabetes (Y-T2D). Results from this follow up study, TODAY2, presented today at the American Diabetes Association’s® (ADA’s) 79th Scientific Sessions® at the Moscone Convention Center in San Francisco, show an accelerating rate of serious complications within the last five years and point to the increased need for more aggressive management of the disease to minimize or prevent the development of serious complications in individuals with Y-T2D.
“Our findings indicate the development of diabetes-related complications in individuals with youth-onset disease is at least as rapid as it is in individuals who develop the disease later on in life. Since these individuals are battling the disease at a younger age, they are experiencing life-changing health consequences caused by type 2 diabetes at the earliest stages of adulthood. This means there will be a substantial burden of diabetes-related complications that will require even more intense management as they age,” said Philip S. Zeitler, MD, PhD, section head of pediatric endocrinology at the University of Colorado School of Medicine and the chair of the department of endocrinology at the Children’s Hospital Colorado.
TODAY was the first multi-ethnic, randomized trial examining individuals who had the onset of type 2 diabetes (T2D) before age 18 years (Y-T2D) and remains unique in this area. When the study began in 2004, it enrolled 699 participants between the ages of 10 and 17 years and sought to compare treatment using metformin (the only FDA-approved medication for T2D in youth), to using metformin combined with rosiglitazone (an oral drug that improves the action of the body’s own insulin), and to using metformin with a lifestyle-intervention program focused on weight loss through healthier eating and increased physical activity. The primary outcome was loss of glycemic control, defined as a glycated hemoglobin level of at least 8% for six months or sustained metabolic decompensation requiring insulin.
Results of the original TODAY study found monotherapy with metformin was associated with sustained glycemic control in approximately half (46.5%) of children and adolescents with T2D. The addition of rosiglitazone, but not an intensive lifestyle intervention, was superior to metformin alone. Detailed analysis of the data further showed non-Hispanic black participants had particularly poor outcomes, with more than 50% having higher than desirable A1C levels within 12 months of initial metformin treatment. Other major outcomes from TODAY include the demonstration that pancreatic insulin secretion decreased at a rate of 20-35% per year, exceeding that reported in adults. In addition, complications and comorbidities were found to be common in this population of individuals with Y-T2D at the time of diagnosis and increased steadily over the time.
At the conclusion of the study in 2011, all TODAY participants were invited to remain in TODAY2, an observational follow-up study. Since then, 517 participants, with a current average age of 25 years and average T2D duration of 12 years, have been seen annually in one of the 15 clinical centers, during which information was gathered using laboratory testing, echocardiograms, vessel function testing, and eye examinations. Researchers also collected the participant’s medical history at each visit to chart any diabetes-related events, such as amputation, heart disease, kidney problems, or vision issues.
Findings from TODAY2 illustrate the occurrence of major diabetes-related events in this young adult population, including heart attacks, chronic kidney disease, advanced diabetic retinal disease, early signs of diabetic nerve disease, and complications in the offspring of pregnancies. Additional results of TODAY2 indicate that more than 50% of the participants had abnormal lipids and more than 60% had high blood pressure. Kidney function assessments show about 40% of participants had evidence for early diabetic kidney disease, and retinal examinations indicate almost 50% of participants had evidence for diabetic retinal disease. Additionally, up to 33% of participants demonstrated early signs of diabetic nerve disease, which was more common in those with worse glucose control. Within the 306 pregnancies reported by participants in TODAY2, 25% of the 236 pregnancies with known outcomes resulted in miscarriage or fetal death, and 24% resulted in preterm births.
“Many of these risk factors and overt complications are not being as vigorously managed as these data suggest is needed,” said Dr. Zeitler. “For example, we found that, despite high blood pressure or abnormal lipids, fewer than half of the participants were on medications to treat these issues. The TODAY2 data suggest healthcare professionals need to overcome hesitancy – whether due to the young age of patients or lack of familiarity with the pharmacotherapy – to aggressively treat young patients battling youth-onset type 2 diabetes to minimize the damage from serious diabetes-related complications. This intensive management depends on coordinated care by teams of providers familiar with the unique aspects of management and the care guidelines for this population.”

Lexicon data for sotagliflozin at American Diabetes Assn

 Lexicon Pharmaceuticals, Inc. (Nasdaq: LXRX), today announced new analyses of clinical data for sotagliflozin will be presented at the upcoming 79th American Diabetes Association (ADA) Scientific Sessions in San Francisco, California. The five accepted posters reflect Lexicon and its collaborator, Sanofi’s efforts to address the unmet need and potential treatment options for the management of type 1 diabetes.
ePosters
  • Saturday, June 8, 11:30am, Exhibit Hall (ePoster Theater B); ePoster Session “The Latest on SGLT Inhibition”
    • Sotagliflozin Reduces Glucose Variability and Risk for Hyperglycemia in Adults with Type 1 Diabetes (1191-P)
    • The Impact of Sotagliflozin on Renal Function, Albuminuria and Blood Pressure in Adults with Type 1 Diabetes (1196-P)
Posters
  • Sunday, June 9, 12:00pm, General Poster Session, Poster Hall (Hall F, North, Exhibition Level)
    • Sotagliflozin Reduces Markers of Arterial Stiffness in T1D:  Pooled Analysis from InTandem1 and InTandem2 Clinical Trials (1212-P)
    • Sotagliflozin Leads to Lower Rates of Clinically Relevant Hypoglycemic Events at Any HbA1c Level at 52 Weeks in Adults with T1D (1220-P)
    • Burden of Cardiovascular Comorbidity in US Adults with T1D (168-LB)
    • ePosters listed above also presented during this session
About Sotagliflozin
Discovered using Lexicon’s unique approach to gene science, sotagliflozin is an investigational oral dual inhibitor of two proteins responsible for glucose regulation known as sodium-glucose co-transporter types 1 and 2 (SGLT1 and SGLT2). SGLT1 is responsible for glucose absorption in the gastrointestinal tract, and SGLT2 is responsible for glucose reabsorption by the kidney.
Zynquista™ (sotagliflozin) has been approved in the European Union for use as an adjunct to insulin therapy to improve glycemic control in adults with type 1 diabetes and a body mass index ≥ 27 kg/m2, who could not achieve adequate glycemic control despite optimal insulin therapy. Sotagliflozin has not yet been approved for use in any other jurisdiction.

Applied Therapeutics to Present on Diabetic Cardiomyopathy Phase 1/2 Trial

Applied Therapeutics Inc. (Nasdaq:APLT), a clinical-stage biopharmaceutical company developing a pipeline of novel drug candidates against validated molecular targets in indications of high unmet medical need, today announced that it will present data at the American Diabetes Association 79th Scientific Sessions in San Francisco (June 7-11, 2019) on AT-001, a novel, potent and selective aldose reductase inhibitor (ARI) in clinical development for Diabetic Cardiomyopathy (DbCM).  The Late Breaking Science poster, entitled “Phase 1/2 Safety and Proof of Biological Activity Study of AT-001, an Aldose Reductase Inhibitor in Development for Diabetic Cardiomyopathy” highlights a recently completed Phase 1/2 study in approximately 120 patients with type 2 diabetes, a subset of which had DbCM.
“Diabetic complications, such as Diabetic Cardiomyopathy, continue to grow despite advancements in glucose control. It’s imperative that therapies are developed to treat or prevent diabetic complications through mechanisms other than glycemic modification,” said Riccardo Perfetti, MD, PhD.  “We are excited to be presenting our data at the prominent ‘Late Breaking’ session at ADA, and are thrilled by the recognition from the congress and the clinical community.  Targeting aldose reductase with a potent and selective inhibitor presents an opportunity to potentially halt disease progression and prevent worsening of heart failure in DbCM patients.  We look forward to initiating our pivotal program for AT-001 in DbCM later this year.”
Phase 1/2 Safety and Proof of Biological Activity Study of AT-001, an Aldose Reductase Inhibitor in Development for Diabetic Cardiomyopathy
(Late Breaking Abstract – oral poster presentation Sunday, June 9, 12-1pm)
  • AT-001 was well tolerated at all doses tested
  • Target engagement was confirmed by potent aldose reductase (AR) inhibition as evidenced by significant reductions in sorbitol, a pharmacodynamic biomarker of AR activity
  • AT-001 improved selectivity and affinity for AR resulted in potent AR inhibition
About Diabetic Cardiomyopathy 
Diabetic Cardiomyopathy (DbCM) is a rapidly progressing degenerative disorder of the heart muscle in people with diabetes. There are no approved therapies for this fatal condition, which affects 17 – 24 percent of people with diabetes, or approximately 77 million patients worldwide. Hyperglycemia, a symptom that characterizes diabetes, triggers the enzyme Aldose Reductase to convert excess glucose into sorbitol and fructose, both of which can lead to cell death in the heart muscle. When this happens, the heart fibroses, or “hardens,” such that the organ is unable to circulate blood through the body effectively. Approximately 25 percent of patients with DbCM progress to overt heart failure or death within 1.5 years of diagnosis.

Icosapent Sets New Standard for Macrovascular Disease Prevention

Just this week, the US Food and Drug Administration (FDA) granted Priority Review to icosapent ethyl (Vascepa), the fish oil-based therapy seeking a supplemental indication for the reduction of residual cardiovascular risks in patients with elevated triglycerides.
When the FDA rules on the Amarin Corporation supplemental application in September, it will make its decision mostly based on the clinical results of the Vascepa CV Outcomes Trial (REDUCE-IT). As a recent review of the long-term, 8000-patient study showed, oral icosapent’s potential in cardiovascular risk reduction may be unprecedented.
The Amarin-supported review, presented at the American Diabetes Association (ADA) 2019 Scientific Sessions in San Francisco, CA, by Robert S. Busch, MD, director of Clinical Research at Albany Medical College, discussed the REDUCE-IT findings both as they pertain to the supplemental application for icosapent as well as its current adjunct hypertriglyceridemia treatment indication.
“Like many of you, I see patients every day,” Busch told his audience at ADA. “And this will change what you do Wednesday morning when you’re back at work.”
It’s fairly common for patients with type 2 diabetes (T2D) to present with raised triglyceride counts routinely, Busch said, requiring physicians to have a viable treatment regimen to manage patient symptoms and elevated cardiovascular risks alongside statins.
In the REDUCE-IT trial—previously presented at the American Heart Association (AHA) 2018 Scientific Sessions—investigators led by Deepak L. Bhatt, MD, MPH, of the Brigham and Women’s Hospital Heart and Vascular Center enrolled 8179 patients with established cardiovascular disease or with diabetes plus other risk factors.
Patients were required to have been receiving statin therapy, as well as a fasting triglyceride level of 135-499 mg per deciliter and a low-density lipoprotein cholesterol level of 41-100 mg per deciliter at baseline.
While assessing for a primary endpoint of a composite of cardiovascular death, nonfatal myocardial infarction (MI), nonfatal stroke, coronary revascularization, or unstable angina, investigators randomly assigned patients to either twice-daily 2 g icosapent ethyl or placebo.
The team also assessed for a key secondary endpoint of composite cardiovascular death, nonfatal MI, or nonfatal stroke.
Primary endpoint event occurred in significantly fewer treated patients (17.2%) than placebo patients (22.0%; HR .75; 95% CI: .65 - .83; P< .001), and the key secondary endpoint was also reached in fewer treated patients (11.2%) than placebo patients (14.8%; HR .74; 95% CI: .65 - .83; P< .001).
Additional ischemic endpoints were also significantly lower in patients treated with icosapent, including the rate of cardiovascular death (4.3% vs 5.2%; HR .80; 95% CI: .66 - .98; P= .03).
A greater rate of patients administered icosapent were hospitalized for atrial fibrillation/flutter, or reported serious bleeding events.
When recounting the significance of the findings, Busch noted the critical need for cardiovascular disease and mortality prevention—at a time when diabetes is reaching epidemic levels, and annual heart disease-driven deaths are climbing. And though much trial data—including those being presented at ADA 2019—evidences better lowering and management of LDL-C with statin monotherapy, residual risk remains unaddressed.
With raised triglyceride levels serving as a reliable indicator of increased cardiovascular risk, clinicians are seeking therapies that capably treat both triglyceride counts and prevent cardiovascular outcomes.
As such, repeated findings showing that icosapent significantly betters both these rates in statin-treated patients has led to broader recognition. The ADA’s 2019 Standards of Care in Diabetes included REDUCE-IT findings to support its designation of icosapent ethyl as an advised treatment for cardiovascular risk reduction among patients with atherosclerotic cardiovascular disease, diabetes, statin-controlled LDL-C, and raised triglyceride levels.
“It’s an obligation and a new standard of care from the ADA to know the triglyceride level in at-risk patients,” Busch said. “And if it’s raised, it’s also now an obligation to prescribe icosapent.”
Busch closed noting that icosapent was associated with “unprecedented” cardiovascular event risk reductions. Whether that’s reflected in the FDA’s decision to support or reject the therapy’s indication will be known in only a few months.
https://www.mdmag.com/conference-coverage/ada-2019/icosapent-macrovascular-disease-prevention

PG&E shuts off power in Sierra Foothills

PG&E has shut off power to about 16,000 customers Saturday night in the Sierra Foothills amid hot, windy conditions to reduce the risk of wildfires. Power was shut off at 9 p.m.
Power was shut off in Butte and Yuba counties, and power may be shut off for El Dorado, Nevada and Placer counties depending on weather conditions.

The shutoff is part of the Public Safety Power Shutoff program to reduce the risk of wildfires.
PG&E expects to restore power Sunday at 8 a.m.
Customers with their power shut off can go to these locations for restrooms, bottled water, electronic device charging and air-conditioned seating.
  • Grass Valley Community Resource Center: Sierra College, 250 Sierra College Drive, Grass Valley, CA 95945
  • Oroville Community Resource Center: Harrison Stadium, 1674 3rd Ave., Oroville, CA 95965
The National Weather Service issued Red Flag Warnings on Friday for the parts of the Central Valley and North Bay Area, leading PG&E to consider the shutoffs.
Power was restored to Solano, Napa and Yolo counties this evening, according to PG&E.