Der neue Bluttest für Fibromyalgie ist zu 99% genau. Jeder muss “Advanced Mold Sanierung” wissen

Ein neuer Bluttest für Fibromyalgie ist genauer als erwartet und wird die chronische Schmerzstörung nicht mit anderen Krankheiten wie Lupus und rheumatoider Arthritis verwechseln, so der Arzt, der den Test entwickelt hat. 
“Wir haben keine Überlappung zwischen den Biomarkern der Fibromyalgie und den Immunsystemprofilen von Patienten mit rheumatoider Arthritis oder Lupus festgestellt. Dies hat den Effekt, dass die Köpfe der Gegner ausatmen”, sagte Dr. Bruce Gillis, Gründer und CEO von EpicGenetics, a bioresearch research company mit Sitz in Santa Monica, Kalifornien.

Ein neuer Bluttest für Fibromyalgie ist genauer als erwartet und wird die chronische Schmerzstörung nicht mit anderen Krankheiten wie Lupus und rheumatoider Arthritis verwechseln, so der Arzt, der den Test entwickelt hat.

“Wir fanden keine Überschneidung zwischen den Biomarkern der Fibromyalgie und den Profilen des Immunsystems von Patienten mit rheumatoider Arthritis oder Lupus. Dies hat die Wirkung, die Köpfe der Gegner auszuatmen “, sagte Bruce Gillis, MD, Gründer und CEO von EpicGenetics, einem Bioresearch-Forschungsunternehmen mit Sitz in Santa Monica, Kalifornien.

EpicGenetics präsentierte den FM-Test im März und nannte ihn den ersten endgültigen Bluttest für Fibromyalgie, eine missverstandene Erkrankung, die durch tiefe Gewebeschmerzen, Müdigkeit, Kopfschmerzen, Depressionen und Schlafmangel gekennzeichnet ist. . Die Ergebnisse der Tests liegen in der Regel in etwa einer Woche vor.

Der FM-Test sucht nach Proteinmolekülen im Blut, den sogenannten Chemokinen und Cytokinen, die von weißen Blutkörperchen produziert werden. Laut Gillis haben Patienten mit Fibromyalgie weniger Chemokine und Zytokine im Blut und haben daher ein schwächeres Immunsystem als normale Patienten.

Kritiker haben angegeben, dass die gleichen Biomarker des Immunsystems bei Menschen mit anderen Krankheiten wie rheumatoider Arthritis gefunden werden können, was den Bluttest unzuverlässig macht.

In einer neuen Studie, an der mehr als 300 Patienten mit Fibromyalgie, Lupus oder rheumatoider Arthritis beteiligt waren, sagte Gillis, dass nur bei Patienten mit Fibromyalgie Chemokin- und Cytokinwerte niedriger als normal waren.

“Sie haben nicht die gleichen Biomarker des Immunsystems. Überhaupt nicht “, sagte Gillis dem National Pain Report. “Die Modelle, die wir bei Lupus und rheumatoider Arthritis sehen, sehen wir diesen Entzündungsprozess. Bei Fibromyalgie sehen wir jedoch nicht die gleichen Biomarker. “

Gillis sagte, die Forschung sei abgeschlossen und hofft, dass sie in einem medizinischen Fachjournal in den kommenden Monaten von Experten überprüft wird.

Als der FM-Test eingeführt wurde, gab EpicGenetics an, bei der Diagnose von Fibromyalgie eine Genauigkeit von 93% zu haben. Gillis sagt, dass die Sensitivität des Tests jetzt auf 99% geschätzt wird, was ungefähr derselbe ist wie der zur Diagnose von HIV verwendete Test.

Dr. Bruce Gillis

Nach Schätzungen der National Institutes of Health leiden 5 Millionen Amerikaner an Fibromyalgie und Millionen von Menschen auf der ganzen Welt. Bisher haben sich nur wenige hundert für den FM-Test angemeldet. Laut Gillis könnten die Kosten von 744 US-Dollar, die im Allgemeinen nicht von der Krankenversicherung gedeckt werden, für viele Patienten ein Hindernis sein.

“Viele Menschen, bei denen Fibromyalgie diagnostiziert wurde, funktionieren nicht. Und weil sie nicht funktionieren, können sie sich einen Test nicht leisten. Sie sind nicht krankenversichert “, sagte Gillis und fügte hinzu, einige Versicherer hätten in Entschädigungsfällen der Arbeitnehmer Beweise gezahlt. 
“Als wir anfingen, kostete es uns 12.500 Dollar, um die Parameter des Immunsystems eines Patienten zu analysieren. Wir senken also die Preise, sehr niedrig. “

Gillis hofft, den Preis für den FM-Test senken zu können, indem andere Laboratorien Blut abnehmen und Blutproben an EpicGenetics senden können.

Unabhängig von den Kosten sind Patienten mit Fibromyalgie auf die Möglichkeit gespannt, dass möglicherweise ein einfacher Test verfügbar ist, um eine Erkrankung zu diagnostizieren, bei der ihre Ärzte und Angehörigen oft skeptisch sind. Es dauert drei bis fünf Jahre, um den Patienten mit einer durchschnittlichen Fibromyalgie zu diagnostizieren.

“Einen zuverlässigen Blutmarker zu haben, wird uns als Patienten mehr als nur bestätigen. Es wird ein Feld voller Träume und Möglichkeiten für mitfühlende Forscher eröffnen, um diese schreckliche Störung zu definieren “, sagte Celeste Cooper, eine Patientin und Patientin der Fibromyalgie.

“Sobald wir einen biologischen Test haben, werden wir wissen, dass die Studienteilnehmer Fibromyalgie haben. Es wird keine voreingenommenen Ergebnisse geben, und die Diskussion über psychische Erkrankungen wird in unserem Untersuchungsspiegel sein. Es ist ein schmackhafter Gedanke. “

In den letzten Monaten gab es mehrere potenzielle Fortschritte bei der Untersuchung der Fibromyalgie.

Forscher im Bundesstaat Ohio befinden sich in einem frühen Stadium der Entwicklung einer anderen Art von Blutuntersuchung auf Fibromyalgie. Mit einem Hochleistungs-Infrarotmikroskop identifizierten sie ein Modell von Molekülen im Blut, das für Patienten mit Fibromyalgie einzigartig zu sein scheint.

Ein anderes Forscherteam im Bundesstaat New York fand heraus, dass Fibromyalgie einen Überschuss an sensorischen Nervenfasern in den Blutgefäßen ihrer Hände aufweist, was den Blutfluss im gesamten Körper unterbrechen kann.

“In weniger als sechs Monaten haben wir zwei Studien erhalten, die über eine erfolgreiche Analyse der Fibromyalgie unter Verwendung von Blutmarkern berichten. Jetzt scheint es, dass es in ein Gebiet geht, das über mehr als eine Debatte hinausgeht “, sagt Cooper.

“Dies ist ein Sieg für die wissenschaftliche Gemeinschaft und ein Sieg für den Patienten. Ich bezweifle, dass dies der letzte ist. Erwarten Sie im Laufe der Rasse mehr Forschung und wie herrlich es für diejenigen von uns sein wird, die jeden Tag mit Fibromyalgie leben. “

Die Forschung könnte auch zur Entdeckung eines genetischen Markers für Fibromyalgie führen, ein Gen, das bei manchen Menschen die Wahrscheinlichkeit erhöht, dass sich die Störung entwickelt.

EpicGenetics rettet zahlreiche Blutproben von Patienten, die den FM-Test bestehen, und hoffte, sie eines Tages analysieren zu können, um Ribonukleinsäure (RNA), Moleküle, die an der Proteinsynthese beteiligt sind, und die Übertragung genetischer Informationen zu ermitteln.

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