Jiaojiao Zhang, Tian Zhao, Hong Lei, Rui Gan et al. identify the transcription factor GABPA as a critical regulator of STING expression, pivotal for antiviral defense and inflammatory diseases. rupress.org/jem/article/...

Jiaojiao Zhang, Tian Zhao, Hong Lei, Rui Gan et al. identify the transcription factor GABPA as a critical regulator of STING expression, pivotal for antiviral defense and inflammatory diseases. rupress.org/jem/article/...
Can Too Much Sugar Cause Diabetes?
Not directly, but by causing overweight it actually can.
But I´m chronic underweight due to #SLE.
health.clevelandclinic.org/can-you-get-...
@clevelandclinic.bsky.social @lupus.org @lupusuk.bsky.social
This One Exercise Can “Significantly” Reduce Waist Size and Weight, Says New Study.
I´m multiply chronic sick, disabled & chronic underweight from #SLE, and I have a chlorine allergy.
I was even freed from the swimming lessons at school for a few years (1980s).
www.thehealthy.com/weight-loss/...
New research found that people with #SLE and depression, anxiety and/or PTSD had higher rates of emergency visits and hospitalizations, highlighting the importance of mental health as part of comprehensive lupus care. Read the study: buff.ly/a5g7ZsV
Metanalysis of Metabolic syndrome (MetS) in #SLE (65 articles, 11K pts). MetS prevalence 27% (higher in males (36 vs 27%). HCQ assoc w/ signif less MetS (OR 0.66), but more w/ CTX (1.39), AZA (1.25), MMF (1.13), but not steroids or MTX. MetS pts were older, obese, w/ high Chol & LDL buff.ly/VQNvSI9
New Research: 70% of People With This Chronic Condition Use Food to Cope.
I don´t, but even if I did it wouldn´t matter, I´m chronic underweight due to #SLE and have been ever since the #Lupus had broken out in 1992...
www.thehealthy.com/news/chronic...
The Best Mattresses for Back Pain, According to Firsthand Testing.
No way, I have a special, extra-soft anti-decubitus foam matress due to my chronic underweight from #SLE, prescribed by my internist.
www.thehealthy.com/pain/back-pa...
For my diabetic online friends.
How Taking a GLP-1 Medication Can Affect Your Face, Body and Overall Appearance.
But I have a very wrinkly face with loose skin too, due to the chronic underweigth from longtime #SLE.
health.clevelandclinic.org/glp-1-appear...
@clevelandclinic.bsky.social
Cluster analysis of Spanish RELES #SLE SLE cohort reveals 3 groups. C1 (n 168) was younger, w/ lupus nephritis, low C3, intensive Rx, high infx & damage. C2 (175) w/ cytopenias, serositis, APL & dsDNA(+). C3 (452) mild skin-Jts, less serologic activity & complications buff.ly/Oj3vuij
Study Identifies Two Molecular Subtypes of Lupus Nephritis and Potential Biomarker for Stratification.
So far I´ve been spared by #LupusNephritis, I hope and pray it´ll remain that way, after more than 34 years with #SLE.
🙏🙏🙏
www.lupus.org/news/study-i...
@lupus.org
Study Highlights Racial Differences in Pregnancy Outcomes Among People With Lupus.
I´m 55 1/2 yet, I never had any kids, but not because of #SLE, it´s because I´m asexual as previous victim of sexual abuse.
www.lupus.org/news/study-h...
@lupus.org
Our "father" deceased from #CFJ in 04/04.
Research We Fund, from the @lupus.org newsletter.
www.lupus.org/for-research...
I´m a German longtime #SLE survivor since 1992, but hadn´t been diagnosed before 08/2002, have been flare-free for 10+ years yet. I´ll #KeepFighting, I´ll #NeverGiveUp.
💖💖💖
bsky.app/profile/mari...
In the 2010s I got additional asthma, and in 07/22 additional ME/CFS. But I #NeverGiveUp, I keep fighting.
My chronic diseases won´t bring me down so fast. I can´t win, but obviously I can keep #SLE at bay,
@lupusuk.bsky.social
Newly Diagnosed? We’re Here for You, I´m an "old" #SLE patient, I´m 55 1/2 now, it broke out in 1992, together with then 2 other auto immune diseases, but wasn´t diagnosed before 08/2002.
Actually I´ve been flare-free for 10+ years so far.
👍👍👍
lupusuk.org.uk/need-to-talk/
@lupusuk.bsky.social
Are You a Young Person Living in Scotland? We Want to Hear From You!
Scottish #Lupus patients can sign up here, I live in Germany and am a longtime #SLE survivor since 1992, but wasn´t diagnosed/treated before 08/2002.
💖💖💖
Waving to UK.
forms.cloud.microsoft/pages/respon...
@lupusuk.bsky.social
I have hypothermia and had it ever since #SLE & Co´d broken out in 1992 yet, right now I´m so cold that I could actually wear fleece or thermo clothes and winter socks yet, as if it was the deepest winter yet.
en.wikipedia.org/wiki/Hypothe...
@wikipedia.org