Watch Aqueous, Members Of moe., Umphrey’s Tear Up Steely Dan’s “Kid Charlemagne” [Pro-Shot]

first_imgOne of the most talked-about highlights in the wake of the annual Summer Camp Music Festival this Memorial Day has been groove rock quartet Aqueous‘s Thursday, 5/25 sunset performance. The set was the first of two full-band slots over the course of the festival (guitarist Mike Gantzer also joined Umphrey’s McGee member Ryan Stasik and Kris Myers for a tribute to Green Day‘s pop-punk classic Dookie), and the Buffalo natives made it count, offering up some incredible improv as well as a couple of very special surprise guests. The previously-planned Dookie set turned out to not be the only Aqueous/Umphrey’s crossover of the weekend, as Aqueous was joined by Umphrey’s keyboardist Joel Cummins as well as moe. drummer Vinnie Amico for a run through Steely Dan‘s 1976 hit “Kid Charlemagne.”You can check out Joel and Vinnie’s guest appearance with Aqueous at Summer Camp below, via Aqueous’s YouTube page:Vinnie Amico, Joel Cummins, and four members of Aqueous are set to take part in the mix-and-match musical mayhem of Brooklyn Comes Alive this coming weekend in Williamsburg, Brooklyn. Aqueous’ Mike Gantzer, Dave Loss, Evan McPhaden and Rob Houk are set for a busy Sunday evening at Brooklyn Comes Alive, as the group will join forces with Vinnie Amico and his moe. bandmate, Al Schnier, for an unforgettable collaborative set of choice covers and material from both of the Buffalo bands’ repertoires–appropriately dubbed moe.queous. That collaboration will go down from 8:30-10pm on Sunday, 9/24 at Brooklyn Bowl, one of three simultaneous venues incorporated in the festival.Aqueous Covers Radiohead and Steely Dan With Members of Umphrey’s McGee [Videos/Photos]Gantzer will also be joining Umphrey’s McGee members Kris Myers and Ryan Stasik to reprise their Dookie set from Summer Camp, promising an energized take on the seminal ’94 Green Day LP, such as “When I Come Around,” “Basket Case,” “Longview,” and “Welcome To Paradise.” In addition to recreating Dookie in its entirety, the band will also perform a handful of other rock classics by bands like Ween, Weezer, and The Ramones at Music Hall of Williamsburg from 11:15 pm – 12:30 pm on Sunday night as one of the festival’s final sets.[Cover photo via Phierce Photo by Keith G (Instagram: @PhiercePhoto)]Inspired by the vibrant musical communities of Brooklyn and New Orleans, Brooklyn Comes Alive is set to take place across three venues in Williamsburg, Brooklyn (Brooklyn Bowl, Schimanski, Music Hall of Williamsburg) on September 23rd and 24th. The unique homegrown event puts the focus on the musicians, curating dream team collaborations, tributes, and artist passion projects for two full days of incredible music both new and old.The 2017 lineup is set to include hand-selected band lineups featuring all-star musicians like John Scofield, George Porter Jr. (The Meters), Bernard Purdie, Aron Magner and Marc Brownstein (The Disco Biscuits), Mike Greenfield and Jesse Miller (Lotus), Jason Hann (String Cheese Incident), Alan Evans (Soulive), Cyril Neville (Neville Brothers), Henry Butler, Reed Mathis (Electric Beethoven), Michael League, Nate Werth, Chris Bullock, Robert “Sput” Searight, and Bob Lanzetti (Snarky Puppy), Jennifer Hartswick and Natalie Cressman (Trey Anastasio Band), and scores of others! ***Tickets Are On Sale Now!***To find out more about ticketing, VIP options, and lodging, head to the festival website.last_img read more

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Is it time to retire cholesterol tests

first_img Click to view the privacy policy. Required fields are indicated by an asterisk (*) In this illustration of a low-density lipoprotein particle, apolipoprotein B (blue) is surrounded by various forms of cholesterol (orange and yellow) and other lipids. Is it time to retire cholesterol tests? By Mitch LeslieDec. 6, 2017 , 2:45 PM Country * Afghanistan Aland Islands Albania Algeria Andorra Angola Anguilla Antarctica Antigua and Barbuda Argentina Armenia Aruba Australia Austria Azerbaijan Bahamas Bahrain Bangladesh Barbados Belarus Belgium Belize Benin Bermuda Bhutan Bolivia, Plurinational State of Bonaire, Sint Eustatius and Saba Bosnia and Herzegovina Botswana Bouvet Island Brazil British Indian Ocean Territory Brunei Darussalam Bulgaria Burkina Faso Burundi Cambodia Cameroon Canada Cape Verde Cayman Islands Central African Republic Chad Chile China Christmas Island Cocos (Keeling) Islands Colombia Comoros Congo Congo, the Democratic Republic of the Cook Islands Costa Rica Cote d’Ivoire Croatia Cuba Curaçao Cyprus Czech Republic Denmark Djibouti Dominica Dominican Republic Ecuador Egypt El Salvador Equatorial Guinea Eritrea Estonia Ethiopia Falkland Islands (Malvinas) Faroe Islands Fiji Finland France French Guiana French Polynesia French Southern Territories Gabon Gambia Georgia Germany Ghana Gibraltar Greece Greenland Grenada Guadeloupe Guatemala Guernsey Guinea Guinea-Bissau Guyana Haiti Heard Island and McDonald Islands Holy See (Vatican City State) Honduras Hungary Iceland India Indonesia Iran, Islamic Republic of Iraq Ireland Isle of Man Israel Italy Jamaica Japan Jersey Jordan Kazakhstan Kenya Kiribati Korea, Democratic People’s Republic of Korea, Republic of Kuwait Kyrgyzstan Lao People’s Democratic Republic Latvia Lebanon Lesotho Liberia Libyan Arab Jamahiriya Liechtenstein Lithuania Luxembourg Macao Macedonia, the former Yugoslav Republic of Madagascar Malawi Malaysia Maldives Mali Malta Martinique Mauritania Mauritius Mayotte Mexico Moldova, Republic of Monaco Mongolia Montenegro Montserrat Morocco Mozambique Myanmar Namibia Nauru Nepal Netherlands New Caledonia New Zealand Nicaragua Niger Nigeria Niue Norfolk Island Norway Oman Pakistan Palestine Panama Papua New Guinea Paraguay Peru Philippines Pitcairn Poland Portugal Qatar Reunion Romania Russian Federation Rwanda Saint Barthélemy Saint Helena, Ascension and Tristan da Cunha Saint Kitts and Nevis Saint Lucia Saint Martin (French part) Saint Pierre and Miquelon Saint Vincent and the Grenadines Samoa San Marino Sao Tome and Principe Saudi Arabia Senegal Serbia Seychelles Sierra Leone Singapore Sint Maarten (Dutch part) Slovakia Slovenia Solomon Islands Somalia South Africa South Georgia and the South Sandwich Islands South Sudan Spain Sri Lanka Sudan Suriname Svalbard and Jan Mayen Swaziland Sweden Switzerland Syrian Arab Republic Taiwan Tajikistan Tanzania, United Republic of Thailand Timor-Leste Togo Tokelau Tonga Trinidad and Tobago Tunisia Turkey Turkmenistan Turks and Caicos Islands Tuvalu Uganda Ukraine United Arab Emirates United Kingdom United States Uruguay Uzbekistan Vanuatu Venezuela, Bolivarian Republic of Vietnam Virgin Islands, British Wallis and Futuna Western Sahara Yemen Zambia Zimbabwe JUAN GAERTNER/SCIENCE PHOTO LIBRARY center_img The next time you go in for a medical checkup, your doctor will probably make a mistake that could endanger your life, contends cardiologist Allan Sniderman of McGill University in Montreal, Canada. Most physicians order what he considers the wrong test to gauge heart disease risk: a standard cholesterol readout, which may indicate levels of low-density lipoprotein (LDL) or non-high density lipoprotein (non-HDL) cholesterol. What they should request instead, Sniderman argues, is an inexpensive assay for a blood protein known as apolipoprotein B (apoB).ApoB indicates the number of cholesterol-laden particles circulating in the blood—a truer indicator of the threat to our arteries than absolute cholesterol levels, some researchers believe. Sniderman asserts that routine apoB tests, which he says cost as little as $20, would identify millions more patients who could benefit from cholesterol-cutting therapies and would spare many others from unnecessary treatment. “If I can diagnose [heart disease] more accurately using apoB, and if I can treat more effectively using apoB, it’s worth 20 bucks,” he says.Sniderman and a cadre of other scientists have been stumping for apoB for years, but recent reanalyses of clinical data, together with genetic studies, have boosted their confidence. At last month’s American Heart Association (AHA) meeting in Anaheim, California, for example, Sniderman presented a new take on the National Health and Nutrition Examination Survey (NHANES), a famous census of the U.S. population’s health. The reexamination, which compared people with different apoB levels but the same non-HDL cholesterol readings, crystallizes the importance of measuring the protein, he says. Across the United States, patients who have the highest apoB readings will suffer nearly 3 million more heart attacks, strokes, and other cardiovascular events in the next 15 years than will people with the lowest levels, Sniderman reported. As lipidologist Daniel Rader of the University of Pennsylvania Perelman School of Medicine puts it, the question of whether LDL cholesterol is the best measure of cardiovascular risk now has a clear answer: “No.” But plenty of scientists disagree. “Many lines of evidence say there’s not a lot more predictive power of apoB over LDL cholesterol,” says cholesterol researcher Scott Grundy of the University of Texas Southwestern Medical Center in Dallas, who has helped craft several sets of cardiology care guidelines. And changing clinical practice would be disruptive. Standard heart disease risk guidelines downplay or omit apoB, and the algorithms that help doctors decide which patients to treat don’t incorporate it.ApoB backers have a new opportunity to make their case. A committee of researchers and doctors is reworking the most influential U.S. recommendations for cholesterol treatment, published by the American College of Cardiology (ACC) and AHA, and should issue an update next year. The European equivalents are also being revamped, although a new version won’t be ready for 2 to 3 years, says cardiologist and genetic epidemiologist Brian Ference of the University of Cambridge in the United Kingdom, who is taking part in the rewrite.Nobody expects these latest revisions to jilt cholesterol for apoB, but its advocates say there’s increasing science on their side. Cholesterol cruises through our blood in several kinds of protein-containing particles, including HDLs, LDLs, and very low-density lipoproteins (VLDLs). When certain particles, such as LDLs and VLDLs, depart the bloodstream and get stuck in the lining of our arteries, atherosclerosis can result. Total cholesterol level was the first widely used indicator of this risk, but after researchers discovered that one form of cholesterol, HDL, may be protective, LDL cholesterol became the benchmark. Now, some physicians favor non-HDL cholesterol, which encompasses multiple cholesterol types, including LDL and VLDL.All of these measures, however, reveal the amount of lipid in the blood, rather than the number of cholesterol-hauling particles. ApoB, in contrast, provides a direct measure of their abundance because each LDL or VLDL particle contains a single copy of the protein.Still, even apoB advocates admit that LDL cholesterol’s track record is pretty good. About 85% of the time, it provides an accurate indication of a patient’s likelihood of developing cardiovascular disease, Ference says. But that means it’s wrong 15% of the time, he adds.A 2009 study found that nearly half of patients admitted to hospitals because of heart attacks had normal or low LDL levels. So by measuring LDL alone, doctors risk overlooking people who need treatment or, if they are already taking drugs to trim their cholesterol levels, a more intensive regimen.At the same time, some people taking drugs for what seem to be dangerously high LDL cholesterol levels may not need treatment, Sniderman says. A more discriminating test for cardiovascular risk could spare these people from potential side effects and save money. Although cholesterol-lowering statins are cheap, Sniderman notes that newer drugs given when statins aren’t enough, such as the PCSK9 inhibitors, can cost tens of thousands of dollars per year.Switching to measuring apoB would improve diagnoses because it better reflects the mechanism of cardiovascular disease, according to Sniderman. “The data support that it’s the LDL particles themselves that are the bad actors,” rather than the cholesterol they contain, Rader says. The more of these particles that course through a patient’s blood, the more get stuck in the arterial walls and the higher the probability of cardiovascular disease. Because LDL cholesterol and apoB are intertwined, both measures give the same result for many patients. However, the amount of cholesterol a particle contains can vary. So LDL cholesterol levels can be misleading for patients who have few large particles or many small ones.No current drugs drive down just apoB, making its impact difficult to untangle from the effect of lowering cholesterol overall. But in a 2015 paper, Sniderman and colleagues reanalyzed data from the famous Framingham Heart Study, which has been probing the causes of cardiovascular disease for nearly 70 years. The patients with the best odds of surviving for at least 20 years had low levels of apoB and non-HDL cholesterol, the team found. But the patients with the worst chances had high levels of apoB, even though their non-HDL cholesterol was low. Similarly, the reassessment of the NHANES data that Sniderman presented at the AHA meeting suggests that apoB is a better predictor of risk.Also pointing to apoB’s importance is a type of analysis in which researchers comb through genetic data from large numbers of patients to identify gene variants that influence a particular trait. Scientists then track the variants’ sway on health, a method called Mendelian randomization because it relies on accidents of heredity to create comparison groups. “It’s essentially nature’s randomized trial,” Ference says. In a study in The Journal of the American Medical Association in September, he and his colleagues dissected the impact of variants of two genes involved in cholesterol metabolism: CETP and HMGCR.Using data from more than 100,000 patients, the researchers found that people with sluggish versions of the enzyme encoded by CETP showed equivalent reductions in apoB and LDL cholesterol levels and were less likely than people with vigorous versions of the enzyme to suffer cardiovascular crises such as heart attacks or strokes. But the scientists saw a telling difference when they analyzed patients who also produced underactive versions of HMGCR’s enzyme. Although these people showed further decreases in LDL cholesterol, their apoB levels—and their cardiovascular risk—didn’t decline by as much. That discrepancy suggests that reducing apoB has a bigger protective effect than lowering LDL, Ference says.The picture is clear, says preventive cardiologist Seth Martin of Johns Hopkins University School of Medicine in Baltimore, Maryland. “The totality of evidence is in favor of apoB being an important marker that can identify risk even when LDL is controlled.”But would the gains be worth the disruption? “The poor frontline primary care doctor doesn’t want to have to think about apoB and non-HDL cholesterol,” says preventive cardiologist and epidemiologist Jennifer Robinson of the University of Iowa in Iowa City, who was vice chair of the committee that drafted the most recent ACC/AHA recommendations in 2013. “It’s too much information—and when you give people too much information they ignore it.”Cardiologist Robert Eckel of the University of Colorado School of Medicine in Aurora, who was also on the ACC/AHA committee, agrees. “I don’t see apoB changing the playing field very much,” he says.Many apoB advocates reluctantly concur. LDL cholesterol is deeply entrenched in medical routines, and “it’s not going to change any time soon,” Rader says. “I go from depression to worse depression,” Sniderman says.But if future guidelines start to emphasize apoB’s diagnostic value and drug companies begin to target it, Ference thinks physicians will eventually pay heed to the protein. “The argument is that LDL cholesterol is good enough,” he says. “But as we move toward more personalized medicine, it’s not.” Sign up for our daily newsletter Get more great content like this delivered right to you! Country Emaillast_img read more

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