Our paper “Increased mortality in community-tested cases of SARS-CoV-2 lineage B.1.1.7” is in Nature today. We find that B.1.1.7, the UK coronavirus variant identified in late 2020, is associated with 55% higher COVID-19 mortality than other lineages. nature.com/articles/s4158… 1/16
The LSHTM team has been analysing B.1.1.7 for signs of increased or decreased severity since late December. We first identified a signal of higher mortality in mid-January. This led to an announcement by the PM and @uksciencechief on 22 January. bbc.co.uk/news/health-55… 2/16
In that early report, we estimated that B.1.1.7 was associated with a ~35% increase in mortality, based on around 2600 deaths, of which 384 had the SGTF marker for B.1.1.7. Our updated analysis is based on 4900 deaths, around 3100 of which had SGTF. 3/16
Using a statistical technique called a Cox proportional hazards model, we found that people infected with B.1.1.7 had a 55% (95% CI 39–72%) higher rate of mortality within 28 days of receiving a positive test. 4/16
The analysis controls for age, sex, deprivation, ethnicity & care home/residential/other residence type. We only compare death rates among people living in the same local authority, who were tested on the same day, to control for changes in test rates and hospital pressure. 5/16
We did not find any statistically significant differences in the increased mortality rate associated with B.1.1.7 by age, sex, IMD, ethnicity, or residence type. 6/16
We did lots of sensitivity analyses. 7/16
While we use a statistical model to account for all the confounding factors, you do not need a model to see that B.1.1.7 is associated with higher mortality in this study sample. The raw data show the pattern clearly. The stats are there to get a clearer estimate. 8/16
I think the most convincing way of looking at the raw data is by comparing the observed number of deaths per follow-up day, stratified here by a number of characteristics. Diamonds higher than circles = increased mortality among subjects with SGTF (the marker for B.1.1.7). 9/16
Our study sample is people tested in the community. If those infected with B.1.1.7 were less likely to get a test, we might only detect severe cases & hence overestimate mortality. But we found no major differences in test seeking (if anything, slight increase for B.1.1.7). 10/16
Other groups working contemporaneously and since have found similar results:
Challen et al bmj.com/content/372/bm…
Grint et al medrxiv.org/content/10.110…
Patone et al medrxiv.org/content/10.110…
Bager et al (Denmark) papers.ssrn.com/sol3/papers.cf…
And others gov.uk/government/pub… 11/16
Overall, the emerging picture is pretty consistent. 12/16
What does this mean? First, it helps to explain why the UK has seen so many COVID-19 deaths in the last three months, together with the increased infectiousness of B.1.1.7, as we described here: science.sciencemag.org/content/early/… 13/16
Second, it adds more evidence that other countries may have a difficult time in the months ahead. Vaccines are effective against B.1.1.7 and will help a lot.
science.sciencemag.org/content/371/65…
papers.ssrn.com/sol3/papers.cf… 14/16
Thanks to: coauthors @Jarvis_Stats John Edmunds @NP_Jewell @karlado @RuthHKeogh; @cmmid_lshtm & @LSHTM; peer reviewers; @rjchallen, @leondanon, SPI-M & NERVTAG for discussions. Big thanks to @PHE_uk for allowing us to release anonymised data: github.com/nicholasdavies… 15/16

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More from @_nickdavies

3 Mar
Our paper “Estimated transmissibility and impact of SARS-CoV-2 lineage B.1.1.7 in England” has now been published in Science (early release: science.sciencemag.org/content/early/…). I’ve tweeted about this a few times before, so I’m going to focus here on some key messages. (1/8)
B.1.1.7 has a 43–90% higher reproduction number than previous SARS-CoV-2 strains. This holds for several different methods we used to analyse its spread, and we found similar rates of increase in the UK, Denmark, Switzerland, and the United States. (2/8) Image
Back in December, we predicted that B.1.1.7 would cause a huge surge in cases and that without stringent measures and faster vaccine deployment, more people in England would likely die from COVID-19 in the first half of 2021 than in all of 2020. (3/8) Image
Read 8 tweets
6 Feb
We've updated our preprint on the transmissibility of SARS-CoV-2 VOC 202012/01, aka B.1.1.7, with new statistical and modelling methods. Headline: we estimate VOC is 43–82% more transmissible than preexisting variants. UNDER PEER REVIEW cmmid.github.io/topics/covid19… (1/6)
We now include new statistical estimates of B.1.1.7 growth, which accord with our earlier model-based estimates—and provide some really interesting plots. (thanks @Alex_Washburne, @inschool4life, @TWenseleers, @seabbs and @sbfnk!) UNDER PEER REVIEW (2/6)
The estimates differ slightly, reflecting the different methods used. But they all identify a significant increase in transmissibility. Of particular note, we found similar growth rates in Denmark. See also, Belgium: UNDER PEER REVIEW (3/6)
Read 6 tweets
1 Jan
@i_petersen Thanks Irene. See image, sorry for bad labelling! Essentially the major pattern is that it doesn't seem to have spread into 80+ quite as quickly. Over November, 0-19s were slightly overrepresented but that seems to have somewhat settled out now. (1/2)
@i_petersen UK scientists originally interpreted this as the variant spreading (slightly) more easily among children than preexisting variants. But with newer data now in, this may have just been a transient effect related to schools being open during the November lockdown. 2/2
@i_petersen I tried to fit way too much into one tweet here. Let me be a bit of a nerd and expand massively on this. First, by UK scientists I mean the scientists on SPI-M who I have been talking to about this, obviously I don't know what the general "UK scientist view" is. a/
Read 6 tweets
31 Dec 20
I can present a brief update to our analyses of VOC 202012/01 from last week. VOC 202012/01 continues to spread in England, as shown in both sequencing data from COG-UK and Pillar 2 testing data provided by Public Health England. NOT PEER REVIEWED 1/7
While the sequencing data above are definitively VOC 202012/01, S-gene target failure (SGTF) is also associated with some other lineages. However, PHE estimates some 98% of SGTF are now VOC 202012/01 (assets.publishing.service.gov.uk/government/upl…). NOT PEER REVIEWED 2/7
Fitting a purely statistical model (logistic growth with a false positive rate representing non-VOC SGTF), we find that the spread of SGTF is consistent with a single increased growth rate for VOC 202012/01 across all NHS regions (grey ribbons). NOT PEER REVIEWED 3/7
Read 7 tweets
24 Dec 20
Just to comment on a few points that have come up in relation to the preprint we put out yesterday on VOC 202012/01, the new variant of SARS-CoV-2 in the UK. ()
Is the apparent spread of VOC due to increased testing? This comes up often when cases rise & indeed case data is subject to biases. But we don't fit to case data in the model. Hospitalisations, deaths, and relative frequency (not abs. number) of the new variant define the trend.
There are other ways of measuring community prevalence besides case data. For example, the ONS just released a new round of estimates based on swabbing random people in England. Also shows increases in prevalence in the 3 regions we highlight to Dec 18. ons.gov.uk/peoplepopulati… Image
Read 6 tweets
23 Dec 20
Late last week, it was announced that a new variant of SARS-CoV-2 (VOC 202012/01) was detected and appeared to be spreading rapidly in the south east of England. We analysed the transmissibility and severity of this new variant. [cmmid.github.io/topics/covid19…] NOT PEER REVIEWED 1/9
We fitted a mathematical model to the growth of VOC 202012/01 in these three regions of England. If current trends continue, the new variant could represent 90% of cases by mid-January. NOT PEER REVIEWED 2/9
We estimate the transmission rate of this variant is 50–74% higher than existing variants; no clear evidence it leads to higher rates of hospitalisation or death. Although rates of both appear slightly higher in the SE, this could easily be noise in the data. NOT PEER REVIEWED 3/
Read 9 tweets

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