Alnylam Uncovers Genetic Mutations in INHBE That Protect Against Abdominal Obesity – Business Wire

CAMBRIDGE, Mass.--(BUSINESS WIRE)--Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNAi therapeutics company, announced today that the Company and collaborators have identified mutations in the INHBE gene associated with protection against abdominal obesity and metabolic syndrome a condition impacting more than 20 percent of adults worldwide. The discovery leveraged sequencing data from more than 360,000 individuals in UK Biobank, and was published in the 13th issue of Nature Communications. The published data show that rare mutations in the liver-expressed INHBE gene are associated with lower waist-to-hip ratio adjusted for body mass index (WHRadjBMI), a surrogate for abdominal fat that is causally linked to type 2 diabetes and coronary heart disease. Findings support the potential of INHBE to be evaluated as a novel therapeutic target for the treatment of cardiometabolic disease. The Company plans to pursue a development candidate for INHBE and its gene product, Activin E, leveraging its liver IKARIA platform.

We are thrilled that our investment in genetic databases like UK Biobank is proving to be fruitful in identifying novel targets in highly prevalent diseases with continued unmet need, said Paul Nioi, Ph.D., Vice President, Discovery and Translational Research, and the Leader of Alnylams Human Genetics Group. There is a well-established causal link between increased waist-to-hip ratio and a persons risk of cardiometabolic conditions. By exploring the genetic determinants of waist-to-hip ratio in this study, important insights into the mechanisms that contribute to body fat distribution were uncovered helping identify potential therapeutic targets for abdominal obesity, like INHBE. The results of this exome-wide analysis suggest that targeting INHBE is predicted to have broad beneficial effects on all facets of metabolic syndrome with potential reductions in the risk of type 2 diabetes and coronary heart disease. We are currently testing this hypothesis, with the goal of pursuing a development candidate targeting INHBE in the near future.

We are delighted to see that the uniquely detailed data within UK Biobank - generously donated by our half a million participants - is accelerating research into important health conditions. Thanks to the collaboration with leading life sciences companies in the UK Biobank Exome Sequencing Consortium, the UK Biobank resource is helping to rapidly identify new therapeutic targets for abdominal obesity, said Professor Naomi Allen, UK Biobank Chief Scientist.

Using whole exome-sequencing data from UK Biobank, Alnylam and collaborators mined for gene variants associated with lower WHRadjBMI in more than 360,000 individuals of European ancestry, revealing loss of function in INHBE as a novel genetic factor contributing to a healthier fat distribution. Rare predicted loss of function (pLOF) variants in INHBE, were carried by one in 587 individuals and were associated with lower abdominal fat. In vitro characterization of the most common INHBE pLOF variant in the study, indicated an approximately 90% reduction in secreted activin E levels. Further analysis of INHBE pLOF carriers revealed a favorable metabolic profile, including decreased triglycerides, increased high-density lipoprotein cholesterol, and decreased fasting glucose. There were no associations suggesting adverse effects of INHBE pLOF, and carriers of these variants did not show evidence of excess mortality. The study also detected associations with lower WHRadjBMI for variants in ACVR1C, encoding an activin receptor, further highlighting the involvement of activins in regulating fat distribution.

About UK Biobank

UK Biobank is a large-scale biomedical database and research resource, containing in-depth genetic and health information from half a million UK participants. The database, which is regularly augmented with additional data, is globally accessible to approved researchers and scientists undertaking vital research into the most common and life-threatening diseases. UK Biobanks research resource is a major contributor to the advancement of modern medicine and treatment and has enabled several scientific discoveries that improve human health.

The UK Biobank Exome Sequencing Consortium (UKB-ESC)

In 2018, Alnylam and partners Regeneron, AbbVie, AstraZeneca, Biogen, and Pfizer announced an agreement with UK Biobank to form the UK Biobank Exome Sequencing Consortium (UKB-ESC), a pre-competitive consortium that aims to sequence the whole exomes of 500,000 volunteer participants in the biomedical resource. The goal of the consortium, which represents the largest ever effort to use genome sequencing to map the DNA of a group of people, is to uncover insights that allow researchers to pinpoint new drug targets at the core of human disease in order to develop effective treatments for patients. To date, the UKB-ESC has made whole-exome sequencing data from 450,000 participants available to the global health community for research purposes and will continue to make all sequenced data available at no cost under the terms of the UKB-ESC charter and the founding principles of UK Biobank.

About Cardiometabolic Disease

Cardiometabolic diseases are the number one cause of death in the world; these include but are not limited to cardiovascular disease, obesity, diabetes mellitus, and non-alcoholic fatty liver disease. An estimated 47 million people in the U.S. alone are living with some form of cardiometabolic disease. Despite the availability of many well-established treatments for cardiometabolic diseases, the substantial mortality associated with this group of diseases underscores the high unmet medical need for new therapeutic options, including those directed to novel disease-modifying targets, and with potential to address poor medication adherence.

About IKARIA Platform

Alnylams IKARIA platform takes advantage of more than two decades of experience in developing RNAi therapeutics. IKARIA enables an extended duration of activity in preclinical studies, with potential for annual dosing in humans, and has design features which provide exquisite specificity, further widening the potential therapeutic index, with enhanced target reduction levels.

About RNAi

RNAi (RNA interference) is a natural cellular process of gene silencing that represents one of the most promising and rapidly advancing frontiers in biology and drug development today. Its discovery has been heralded as "a major scientific breakthrough that happens once every decade or so," and was recognized with the award of the 2006 Nobel Prize for Physiology or Medicine. By harnessing the natural biological process of RNAi occurring in our cells, a new class of medicines, known as RNAi therapeutics, is now a reality. Small interfering RNA (siRNA), the molecules that mediate RNAi and comprise Alnylam's RNAi therapeutic platform, function upstream of todays medicines by potently silencing messenger RNA (mRNA) the genetic precursors that encode for disease-causing or disease pathway proteins, thus preventing them from being made. This is a revolutionary approach with the potential to transform the care of patients with genetic and other diseases.

About Alnylam Pharmaceuticals

Alnylam (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and prevalent diseases with unmet need. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach yielding transformative medicines. Since its founding 20 years ago, Alnylam has led the RNAi Revolution and continues to deliver on a bold vision to turn scientific possibility into reality. Alnylams commercial RNAi therapeutic products are ONPATTRO (patisiran), GIVLAARI (givosiran), OXLUMO (lumasiran), AMVUTTRA (vutrisiran), and Leqvio (inclisiran) being developed and commercialized by Alnylams partner, Novartis. Alnylam has a deep pipeline of investigational medicines, including six product candidates that are in late-stage development. Alnylam is executing on its Alnylam P5x25 strategy to deliver transformative medicines in both rare and common diseases benefiting patients around the world through sustainable innovation and exceptional financial performance, resulting in a leading biotech profile. Alnylam is headquartered in Cambridge, MA. For more information about our people, science and pipeline, please visit http://www.alnylam.com and engage with us on Twitter at @Alnylam, on LinkedIn, or on Instagram.

Alnylam Forward Looking Statements

Various statements in this release concerning Alnylam's future expectations, plans and prospects, including, without limitation, Alnylams views with respect to pursuing INHBE as a therapeutic target for cardiometabolic disease and its goal to identify a development candidate targeting INHBE in the near future, Alnylams aspiration to become a leading biotech company, and the planned achievement of its Alnylam P5x25 strategy, constitute forward-looking statements for the purposes of the safe harbor provisions under The Private Securities Litigation Reform Act of 1995. Actual results and future plans may differ materially from those indicated by these forward-looking statements as a result of various important risks, uncertainties and other factors, including, without limitation: the direct or indirect impact of the COVID-19 global pandemic or any future pandemic on Alnylams business, results of operations and financial condition and the effectiveness or timeliness of Alnylams efforts to mitigate the impact of the pandemic; the potential impact of the recent leadership transition on Alnylams ability to attract and retain talent and to successfully execute on its Alnylam P5x25 strategy; Alnylam's ability to discover and develop novel drug candidates, including a development candidate targeting INHBE, and delivery approaches, and successfully demonstrate the efficacy and safety of its product candidates; the pre-clinical and clinical results for its product candidates; actions or advice of regulatory agencies and Alnylams ability to obtain and maintain regulatory approval for its product candidates, as well as favorable pricing and reimbursement; successfully launching, marketing and selling its approved products globally; delays, interruptions or failures in the manufacture and supply of its product candidates or its marketed products; obtaining, maintaining and protecting intellectual property; Alnylams ability to successfully expand the indication for OXLUMO, ONPATTRO and AMVUTTRA in the future; Alnylam's ability to manage its growth and operating expenses through disciplined investment in operations and its ability to achieve a self-sustainable financial profile in the future without the need for future equity financing; Alnylams ability to maintain strategic business collaborations; Alnylam's dependence on third parties for the development and commercialization of certain products, including Novartis, Sanofi, Regeneron and Vir; the outcome of litigation; the potential impact of current and the risk of future government investigations; and unexpected expenditures; as well as those risks more fully discussed in the Risk Factors filed with Alnylam's most recent Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission (SEC) and in its other SEC filings. In addition, any forward-looking statements represent Alnylam's views only as of today and should not be relied upon as representing its views as of any subsequent date. Alnylam explicitly disclaims any obligation, except to the extent required by law, to update any forward-looking statements.

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Alnylam Uncovers Genetic Mutations in INHBE That Protect Against Abdominal Obesity - Business Wire

SOPHiA GENETICS to Participate in Canaccord Genuity 42nd Annual Growth Conference – StreetInsider.com

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BOSTON and LAUSANNE, Switzerland, July 29, 2022 (GLOBE NEWSWIRE) -- SOPHiA GENETICS SA (Nasdaq: SOPH), a leader in data-driven medicine, announced today Chief Financial Officer, Ross Muken, will attend and be a panelist at the Canaccord Genuity 42nd Annual Growth Conference on Thursday, August 11, 2022 at the InterContinental Hotel in Boston, MA, United States.

Ross will join other industry leaders for the panel Leveraging Omics-Based Data and Analytics to Advance Precision Health to the Next Level, starting at 9:30 a.m. EST.

A live webcast and replay of the session will be available on the investor relations section of the SOPHiA GENETICS website at https://ir.sophiagenetics.com.

About SOPHiA GENETICSSOPHiA GENETICS (Nasdaq: SOPH) is a healthcare technology company dedicated to establishing the practice of data-driven medicine as the standard of care and for life sciences research. It is the creator of the SOPHiA DDM Platform, a cloud-native platform capable of analyzing data and generating insights from complex multimodal data sets and different diagnostic modalities. The SOPHiA DDM Platform and related solutions, products and services are currently used by more than 790 hospital, laboratory, and biopharma institutions globally. For more information, visit SOPHiAGENETICS.COM, or connect on Twitter, LinkedIn and Instagram. Where others see data, we see answers.

Investor Contact:Jennifer PottageHead of Investor Relations[emailprotected]

Media Contact:Don GranesePublic Relations[emailprotected]

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SOPHiA GENETICS to Participate in Canaccord Genuity 42nd Annual Growth Conference - StreetInsider.com

Views of Canadian healthcare professionals on the future uses of non-invasive prenatal testing: a mixed method study | European Journal of Human…

Views of Canadian healthcare professionals on the future uses of non-invasive prenatal testing: a mixed method study | European Journal of Human Genetics  Nature.com

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Researchers find new genetic mutation causing autism through study of patients and families – KBR

A Seoul National University Bundang Hospital (SNUBH) research team has discovered a new gene mutation related to the cause of autism for the first time worldwide through a large-scale genetics study of autistic patients and their families.

Autism is a developmental disorder characterized by repetitive behavior or narrowness of interest along with a lack of communication or social interaction, as shown in the popular drama "Extraordinary Attorney Woo." Typically, characteristic symptoms are revealed around the age of 2. Considering the brain develops quickly, early intervention is important.

Genes play a major role in the development of autism, but the specific genes and their role in early brain development have not been identified. Consequently, there are no treatments for autism symptoms, such as social deficits or communication disorders, but only medication to cure impulsivity or anxiety symptoms.

Professor Yoo Hee-jeong of the Neuropsychiatry Department at SNUBH conducted the joint study with Professors Lee Jeong-ho and Choi Jun-kyun of the Korea Advanced Institute of Science and Technology (KAIST), Institute of Basic Science Director Kim Eun-joon, and others to identify the genetic mutations that cause autism for the development of therapeutics.

The joint group focused on the brains non-coding region, a genomic region that accounts for more than 98 percent of the genomic data but was excluded from the study as it does not directly produce proteins. Researchers received blood from 813 people autism patients and their family members suitable for the study and analyzed the genome, produced human stem cells to reproduce prenatal neurons.

Results revealed that genetic mutations in the non-coding region affect brain development by remotely influencing distant genetic mutations through interactions in three-dimensional spaces in early stages of neurodevelopment.

This study changes the autistic research paradigm, which previously focused only on areas encoding existing proteins, and reveals new target genes to determine the root cause of autism. Professor Yoo said.

Yoo added that the team has identified the hidden secret of autism using data unique to Koreans' autism parties and families and are very grateful for the dedication of the participants in this study.

We will continue research to help improve the lives of autistic people and their families, Yoo said.

The study was published in the latest issue of the Molecular Psychiatry journal.

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Researchers find new genetic mutation causing autism through study of patients and families - KBR

Grey’s Anatomy Vet Cheers ‘Classic Cast’ Plus the Flurry of ‘Exciting and Gorgeous’ Additions for Season 19 – TVLine

Greys Anatomys influx of five (count em, five) cast additions for Season 19 are exciting as well as gorgeous, says series vet Caterina Scorsone.

As announced in recent weeks, a quintet of first-year surgical residents are about to roam the halls of Grey Sloan Memorial this fall. You have Adelaide Kane (Reign) as Jules Millin, who was raised by drug addled artist/hippies and somehow emerged as the only real grown-up in the family, plus Harry Shum Jr. (Glee) as Daniel Blue Kwan, a sharp-witted, impatient and brilliant resident who is generous by nature but competitive to a fault.

Also new for Season 19 are Niko Terho who starred opposite Greys Jake Borelli in the 2020 Freeform movie The Thing About Harry as Lucas Adams, who is determined to prove himself as a surgeon (just like many in his family that have come before him), and Midori Francis (Sex Lives of College Girls) as Mika Yasuda, a middle child with eight siblings who is used to being overlooked and underestimated (and uses it to her advantage).

Last but perhaps most curiously, you have Alexis Floyd (Inventing Anna) playing Simone Griffin, a high-achieving and whip-smart young woman who grew up in Seattle but never wanted to work at Grey Sloan because of a painful personal history with the hospital.

Series vet Scorsone, who plays Amelia, tweeted on Saturday night that she had the season premiere script in hand and was memorizing her lines, before adding, The classic cast is ready and revving. The new cast additions are exciting and gorgeous. Inside and out.

Are you as excited for the infusion (transfusion?) or new blood for Greys Anatomy Season 19?

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Grey's Anatomy Vet Cheers 'Classic Cast' Plus the Flurry of 'Exciting and Gorgeous' Additions for Season 19 - TVLine

Harry Shum Jr. Joins Greys Anatomy For Season 19 – Deadline

EXCLUSIVE: Glee alum Harry Shum Jr. rounds out the group of five new resident cast additions for the upcoming 19th season of ABCs venerable medical drama Greys Anatomy. He joins recently cast Adelaide Kane, Alexis Floyd, Niko Terho and Midori Francis. All five will play first-year surgical residents at Grey Sloan, which was ordered to disband and rebuild its teaching program in the Season 18 finale.

Primetime-Panic

Your Complete Guide to Pilots and Straight-to-Series orders

Shums Daniel Blue Kwan is sharp-witted, impatient and brilliant. He is generous by nature but competitive to a fault, naturally gifted, and used to winning at everything. A family crisis interfered with his career plans and now hes got a lot to prove.

The character description hints at a backstory that would explain why Daniel is a little older than your typical medical resident.

Known for his roles in Foxs Glee and Freeforms Shadowhunters, Shum alsostarred in, produced and co-choreographed The LXD (Legion of Extraordinary Dancers), a Hulu dance series created by Jon M. Chu who also directed Shum in the hit movie Crazy Rich Asians. Hes next set to reprise his Crazy Rich Asians role of Charlie Wu in the upcoming spinoff movie which centers around Gemma Chans character of Astrid Young Teo and her romance with Charlie.

Shum plays one of the leads in this years breakout indie hit Everything Everywhere All at Once. He also stars in and executive produces technological thriller Broadcast Signal Intrusion, which premiered at SXSW and had a domestic theatrical/VOD release in fall 2021. It is now available on-demand. Last year, Shum starred alongside Nina Dobrev and Jimmy O. Yang in Netflixs holiday movie Love Hard.

Additionally, Shum has partnered with The Conscious Kid and is working with the organizations Anti-Racist Childrens Book Education Fund initiative. He is repped by Paradigm, Triniti Management, and Goodman, Genow, Schenkman, Smelkinson & Christopher.

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Harry Shum Jr. Joins Greys Anatomy For Season 19 - Deadline

Multimodal anatomy of the human forniceal commissure | Communications Biology – Nature.com

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Multimodal anatomy of the human forniceal commissure | Communications Biology - Nature.com

Latest Iteration of Nike Air Max 95 "Anatomy of Air" Highlights the Human Spine – HYPEBEAST

Nike continues to expand its offering for the Air Max 95 Anatomy of Air collection. In the past, the sportswear giant released a shoe in a color palette that mimics layers of muscle, never and bone. This particular release has been revealed to highlight the human spine for its latest iteration.

The classic silhouette comes dressed in a color scheme makeup of Brown Basalt, University Red and Oxen Brown. Constructed with a mixture of premium materials, the shoes layered upper is also reminiscent of earthy tones, giving the shoe a rugged aesthetic fit for outdoor adventures. Connecting to the Anatomy theme, the lumbar spine anatomy is visible all along the heel of the shoe.

Look out for the pair arriving soon in select retailers and on Nike for $180 USD.

Elsewhere in footwear, rumors of an A Ma Manire x Air Jordan 4 collab have surfaced.

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Latest Iteration of Nike Air Max 95 "Anatomy of Air" Highlights the Human Spine - HYPEBEAST

Anatomy of a thunderstorm shows why storms come and go in a flash – WUFT

Florida sees an abundance of thunderstorms in the summer season. According to the National Weather Service, Florida can report 70 to 100 days with thunderstorms a year.

The temperature of the surface of the Earth heats rather quickly, which allows for the atmosphere to reach convective temperature, which in turn allows for cumulous clouds to develop,FPRENMeteorologist Justin Ballard said. The taller the cloud, the more likely there is to be charge-separation, which leads to lightning.

In Florida, we tend to see afternoon storms form and dissipate rather quickly. These storms can pop up without much warning, and that makes them hard to forecast.

NWS Jacksonville shows in this tweet how wildly different conditions can be depending on your location, from rain on the left side of the photo to no rain on the right, Ballard said. The rain-cooled air then hits the ground and spreads out. Those outflow wind gusts, as we call them, can act as miniature cold fronts which lift warm air and produce additional thunderstorm development elsewhere.

This pattern produces the foot-shaped formation seen in the photo, typical of pulse thunderstorms. Pulse thunderstorms refer to the kind of storms that are not associated with sea breeze boundaries, Ballard said. Meanwhile, sea breeze thunderstorms form because of a convergence of air along the coastline. Pulse thunderstorms generally dont form like this, they typically pop up and dissipate within an hour.

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Anatomy of a snowball: Paul Pogbas injury and what to do next – Black & White & Read All Over

Victor Laszlow had just led the bar in a stunning, tearful rendition of La Marseillaise. The place is buzzing. Major Strasser, alarmed at the display, orders Captain Renault to close the establishment, leaving the police captain to utter one of Casablancas many immortal lines:

But everyone is having such a good time!

Thats how I felt as I first read that Paul Pogba had left training due to an injury a day after he was so impressive in his first game back in a Juventus shirt last week against Chivas. Its the feeling that bounced around my brain every time a new report rocketed around the Twittersphere, each one adding heft to the snowball rolling down the hill. What was initially reported as an innocuous training knock suddenly turned into two months on the sidelines, which in turn suddenly transformed into the prospect of not seeing Pogba play a meaningful game for Juventus until 2023.

As the shock of such a crazy turn of events wears off, dejection is replaced with a bunch of questions, the most important of which is, what should the team do next?

A lot still depends on the final evaluation of Pogbas knee.

If the injured meniscus is indeed as bad as the doomsayers in the media say it is, Pogba will then have a decision to make as to how he wants to handle it. He could either have the injured piece of cartilage removed, or he can have it repaired. The former would get him back on the field quicker, but could lead to even more problems down the road. The latter would likely result in a more stable joint, but would keep him out until the new year and, critically, rule him out for Frances defense of their World Cup title in Qatar.

Its a big question, to be sure. But as an observer, there is a large part of me that wonders why Juventus even let ourselves get into this mess in the first place. I, for one, had always been a little bit leery of Pogbas recent injury history one that over the last two years had been even worse than that of Paulo Dybala, the man hes essentially replacing on the roster. There have been scattered reports suggesting that Pogbas injury problems at Manchester United stemmed in large part from issues with his knee that compounded until the current tear finally formed.

We need to be clear that thats not at all confirmed, BUT, if it is in fact the case, it raises a ton of additional questions. If Pogbas knee was already unstable, how did Juves medical staff, which was overhauled and supposedly improved after the shocking number of injuries the team dealt with last season, miss that in his medical? If they did, that suggests a stunning level of incompetence. If they didnt, then it indicates that the front office thought they could somehow ride it out, which suggests either arrogance, wishful thinking, or a bit too much focus on off-field matters, which, at least in my eyes, would deduct a few points from the ledger of the Maurizio Arrivabene/Federico Cherubini regime.

Regardless of how it ended up coming about, the fact is that its happened, and now the team is going to have to deal with the aftermath. Assuming the worst, and that Pogba is out for the medium- to long-term, how does the team go about replacing him?

We discussed this for a while in this weeks episode of The Old Lady Speaks, but that was before the prospect of Pogba being out until after the World Cup was a thing. At the time, the idea of riding this out with the midfielders on the squad was more plausible, but in the worst case scenario some more depth is going to be necessary. That could come in the form of keeping all three of the Miretti-Fagioli-Rovella triumvirate, with the potential to loan them out for playing time come January. It could also come from without. Leandro Paredes has been linked with a potential move to Turin all summer, and Radio Radio has reported that the club has approached Roma about the availability of another Frenchman, Jordan Veretout, who is surplus to requirements at Trigora.

How Juve decides to address the depth chart will also go a long way to seeing how Pogbas spot in the starting XI is filled.

Going into the season, Pogba was one of two locks in the midfield, along with Manuel Locatelli. How the midfield lines up in his absence will depend on a couple of things. The presence of Adrien Rabiot is one of them. If he is on the roster for the first game of the season, hes almost certainly going to be the starter on the left side of midfield. The only scenario where this wouldnt be the case is if hes held out pending an imminent transfer, which is entirely possible, as it looks as though his entourage has been trying to engineer a move away from Turin this summer. But if hes a functional piece of the roster, Allegris track record with using him suggests hed get the first crack, with Locatelli playing as regista and the right side manned by either Weston McKennie and Denis Zakaria.

The other variable comes with the potential acquisition of Paredes. Allegri seems dead set on using a traditional regista this season. If Paredes were to arrive, he would be the best fit for that role by quite a ways. That would kick Locatelli onto one of the flanking midfield position and leave the other to some combination of the remaining players.

Theres also the chaotic option of simply throwing caution to the wind and allowing Miretti, Fagioli, and Rovella to ball while Pogba is out. At least one of the three is likely headed out on loan Rovella has multiple suitors at the moment and Allegris dinosaur-ish views about young players almost certainly puts them behind the likes of McKennie, Zakaria, and Rabiot as a solution to the problem. But Pogba himself was allowed the room to break out and become the player he became after an injury to Claudio Marchisio opened up an opportunity. Fagioli and Rovella have both played well in preseason, and Miretti showed Allegri his quality right in front of his face at the end of last season. All of them are eminently capable of following in Pogbas footsteps and proving themselves on the big stage. All it will take for one of them to do so is an opportunity.

But before all this clicks into place, well need to know the basics: how bad, and how long? But, given the amount of money Pogba is being paid and his importance to the team, one certainly hopes that this isnt the beginning of a depressing trend.

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Anatomy of a snowball: Paul Pogbas injury and what to do next - Black & White & Read All Over