I want to discuss several factors to be considered when choosing
antibiotics in the management of Lyme disease.
There is a lot of confusion about the basic biology of the
Lyme spirochete, Borrelia burgdorferi. A lot has been worked out but there is
some confusion and misinformation on the internet.
Lyme is primarily an extracellular bacterium and resides in
spaces between the cells, extracellular matrix. Without question Lyme
spirochetes are occasionally intracellular but this is not the pathogen’s
primary modus operandi. Not primarily
intracellular.
Lyme is pleomorphic – takes on various forms and has modes
of persisting. It forms round forms sometimes
called cysts and congregates within
biofilms. Does not form L-forms. Discussed
elsewhere.
There are many classes of antibiotics. Antibiotics within a
class share features, typically chemical structure and mode of action. I will
mention a few examples.
The macrolide story is interesting. Zithromax and Biaxin are the two clinical
agents of this class most used. On the face they sound similar. Both work by an
intracellular mechanism inhibiting protein synthesis. But clinically there are differences. Biaxin is more effective against Lyme and
Zithromax is more effective against other organisms, for example Babesia.
Zithromax has a unique and well-known ability to concentrate
inside cells many times the concentration in serum. Because Lyme is primarily extracellular this quality
is not a critical factor. Otherwise Zithromax would be much more effective than Biaxin.
When evaluating the effectiveness of an antibiotic against a
particular bacterium, test tube, in-vitro data is cited. Numbers include: MIC (minimal inhibitor concentration), MBC
(minimal bactericidal concentration). The time during which the antibiotic
concentration exceeds the minimum kill level is called AUC, area under curve.
These numbers estimate what may happen in humans taking the drugs. The numbers have limitations and can mislead.
Doxycycline is a favorite drug. It is extremely bioavailable
and easily reaches a steady state in the blood stream. For this reason, many
experts claim there is no reason to ever give the drug IV. Not true. There is
evidence that tissue levels are much higher when the drug is given IV. Our
target is tissues where the germ resides – not the blood.
Antibiotics may be: bactericidal, kill the bacteria or bacteriostatic
stop their growth. In clinical practice there
is no difference.
Antibiotics may interact with bacteria in diverse ways. In
most cases a sustained blood level is preferred, example, B lactam drugs,
amoxicillin and Ceftin. In other cases,
drugs are more effective when there is a distinct peak serum level, as in the
case with gentamicin, used for Bartonella.
Lyme has persister forms and is difficult to eradicate at best. Strategies to eliminate persister forms have including antibiotic cocktails and pulsing. Doctors have various theories and preferences.
Questions to consider when choosing an antibiotic:
1)
What germ(s) are we targeting? What is the
pathobiology of the germ? Big word. How does the pathogen make us sick? Where
does the target germ reside?
2)
Does the antibiotic reach the target(s)?
3)
Is the antibiotic bioavailable (get into blood
stream)?
4)
Does the antibiotic offer the right “killing
kinetics?” This asks if there is a
steady state versus a sharp peak and trough levels, as desired, based on the pharmacology
of the antibiotic.
5)
Oral or intravenous therapy?
6)
Continuous or pulse therapy?
7) Single therapy or combination therapy and how to proceed?
7) Single therapy or combination therapy and how to proceed?
There are many other factors and considerations. For
example, when used in combination antibiotics may exhibit synergy, mechanism
unknown. Drug combinations may be toxic or
cancel out the efficacy of the other. For example, rifampin reduces the effective dose of Mepron by 50%.
Figuring
out how best to treat infections is complicated. Standard therapies may be poorly explained and not be effective. We may have to go a step or 10 further. But there should be a method to the
madness.
Hi LymeMD.
ReplyDeleteDo you know if minocyclone inhibit cefotaxime? I'm currentlly taking 300 mg of minocycline with 6 gr of cefotaxime daily but i don't know if it has interaction and i can't find it in any page.
Thank you.
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