BCA-clinic Betriebs GmbH & Co. KG Dr. med. Armin Schwarzbach Facharzt für Labormedizin
Increasing importance of co-infections for Lyme disease patients – with or instead of a Lyme disease infection An article by Armin Schwarzbach,M.D., PhD., laboratory medicine specialist
In the past months presentations of scientific conferences have shown a noticeable increase of the importance of co-infections and all tick-born diseases and reactivated infections respectively specific regarding laboratory diagnoses and resulting therapy decisions. Prof. Sievers reported at the annual meeting of the German Borreliosis and FSME Association that according to current research in Switzerland that the examined ticks had 42% Rickettsia and “only” 34% Borrelia and 1% Ehrlichia/Anaplasma. According to him in Switzerland approximately 16% of all Lyme patients additionally suffer from Rickettsia (with pericarditis and muscle pain) due to the high contamination of ticks with Rickettsia in Switzerland. According to Dr. Lindauer, Tick-laboratory Weiden, in Germany, app. 6% of all ticks are contaminated with Ehrlichia and Babesia. Babesiosis, Anaplasmosis and other co-infections are increasingly considered in diagnosis and therapy in the USA as well. (Presentation JJ. Burrascano “What´s new!” Sept. 2008). In the BCA-clinic Augsburg (BCA) a laboratory test to check for co-infections is also performed for patients who are diagnosed with Lyme disease because of their clinical results and in case of a specific suspicion. It should be noted that many symptoms of co-infections are the same as Lyme disease symptoms. Therefore, a precise decision of the therapists about the antibiotic therapy cannot be made unless possible co-infections were checked for. Not all co-infections are sensitive to all commonly used antibiotics for Lyme disease. Testing for possible co-infections might result in an increase of the laboratory cost (up to € 950). But these are justified by the additional reliability of the diagnosis and especially by choosing the right antibiotic treatment, i.e. more success promising antibiotic therapies as well as generally less extensive costs for the medication during the antibiotic treatment (vs. the “classical” antibiotic treatment in case of chronic Lyme disease). It has to be noted that in the meantime cellular activity tests, besides the Borrelia Lymphocyte Transformation Test (LTT), have also been developed for Ehrlichia/Anaplasma, Chlamydia pneumoniae and Chlamydia trachomatis via the Elispot-LTT-technique and in the near future for Babesia, too. Actual cellular activity can be measured with Elispot-LTT- technique. And – with the help of these new Elispot-LTT techniques numerous activities of Chlamydia and Anaplasma were discovered in the BCA! Parallel to this, an examination of antibodies in the serum regarding the co-infections is performed. By now there are very well standardised antibody tests for Chlamydia, Mycoplasma, Ehrlichia, Bartonella, Rickettsia, Babesia, Yersinia, etc. Here applies the same as for the Borrelia-LTT: antibodies alone do not predict the disease activity as a single testing – the Elispot-LTT, however, can provide evidence because with this test documents the interferon release against the particular co- pathogens in the blood. It should be noted that in some cases it is the co-infection pathogen itself that is responsible for symptoms and not the Lyme infection: Chlamydia, for example, create disease patterns
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such as Morbus Alzheimer, Multiple Sclerosis, Fibromyalgia, Chronic Fatigue Syndrome (CFS), myocardinal infarct, strokes, blood vessel inflammations and visual disturbances. The Lyme infection might have been successfully treated already with antibiotics, but the co- infection has not yet been destroyed by the antibiotics. Therefore, a detailed anamnesis of the symptoms needs to be documented before, during and after an infection with borrelia or other bacteria. Not all possibly remaining symptoms are due to Lyme after an antibiosis, but could be due to a co-infection!
Infectiology will gain a considerable dominant position in medicine – among others due to climate change – and this does not only apply to tick-borne diseases. A note on: Contamination of ticks in Switzerland (current data)
16 % Borrelia afzelii 11 % Borrelia garinii 5 % Borrelia sensu stricto
(causes myalgia, pericarditis) 17 % of Borrelia contaminated ticks have additional Rickettsia! 14 out of 113 Lyme disease patients additionally have Rickettsia symptoms! Source: Presentation by Prof. Sievers, Hochschule Wädenswil, 5.4.2008 Bad Soden-Salmünster
Overview of the most frequent co-infections of Lyme Disease
– Ehrlichia – Babesia – Bartonella – Rickettsia – Chlamydia – Mycoplasma –
Ehrlichia/Anaplasma
Pathogen: Anaplasma phgocytophilum (gram-negative, obligatory intracellular in granulocytes)
Spectrum of hosts: wild animals (e.g. deer), domestic animals, productive livestock, humans
Symptoms: (incubation period: days up to 4 weeks):
Flu-like symptoms with fever, headaches and muscle pain with “sharp and stabbing, often located behind the eyes”, neurologic symptoms (duration 1 up to 60 days) up to lethal ending, sometimes diffuse erythema (reddening of the skin) including palms of hands and soles of feet
Risk factors: elderly people, severe basic underlying diseases, immune suppression
Activity test: Elispot®-LTT (Lymphocytes transformation test)
Ehrlichia-PCR in blood (EDTA-blood): direct detection
Antibodies for Ehrlichia-IgM and Ehrlichia-IgG: indirect detection – control of progression!
Macrolides (Azithromycin, Clarythromycin) Tetracycline (Doxycycline, Minocycline) Quinolones (Ciprofloxacin, Levofloxacin) Rifampicin (During pregnancy!)
Babesia
Pathogens: Babesia microti, Babesia divergens
Vector/Transmission: Ixodes ricinus, blood transfusion
Spectrum of hosts: wild animals (e.g. deer), domestic animals, productive animals, humans
Symptoms: (incubation period 5 days – 9 weeks):
Sweating, neck stiffness, nausea, vomiting, loss of appetite, fatigue, feeling of weakness, constant exhaustion especially during stress, haemolytic anaemia, haemoglobinnuria, fever up to 40º C, shivering, sometimes hepatosplenomegaly, muscle pain, strong headaches, dizziness, coagulation dysfunction (blood-clotting disorder, hypercoagulability), stomach ache, emotional instability, mental dullness, kidney failure, dyspnoea, influenza-flu-like symptoms (up to a lethal level)!
Risk factors: Splenectomia, HIV, immune suppression, organ transplantation, elderly people
Babesia-PCR in blood (EDTA-blood): direct detection
Antibodies of Babesia-IgM and Babesia-IgG: indirect detection – control of progression !
- Hamolytic anemia (erythrocytes, haptoglobin) - Thrombocytopenia - Leucocytopenia - Increase of liver parameters (sGOT, sGPT, sGGT) - Increase of Creatinine, Urea - Hemoglobinuria
Clindamycin Malarone 250/200 mg 1x/day Malarone junior 65/25 mg 1x/day Atovaquone 750 mg 2x/day Lariam 250 mg
Bartonella
Bacteria: Bartonella henselae (gram-negative, optional intracellular in endothelial cells /
Erythrocytes) and/or BLO = Bartonella like organisms
Vector/Transmission: surface wounds/scratch from cats, Ixodes ricinus
Symptoms (incubation period 3 – 38 days):
headache (80%), fatigue (100%), muscle twitches, tremors, cramps, shivering, fever in the mornings (30%, in thrusts up to 6 weeks, otherwise 1 – 3 weeks), swollen lymph nodes, arthralgia (often), myalgia, insomnia, depression, agitation, amentia, concentration and attention disorder, dizziness, restlessness, gastritis, intestinal problems, sore feet soles (especially in the morning), hypodermic nodules along the extremities, no or minimal joint pain (important according to J.J. Burrascano)
Severe progression: endocarditis, retinitis, epilepsy, aseptic meningitis, hepatosplenomegalia
- PCR on Bartonella in blood (EDTA-blood): direct detection - Histology (hemangiome/lymphadenitis) - Antibodies on bartonella henselae-IgM and bartonella henselae-IgG: indirect
detection evidence – control of progression !
- Elevated vascular endothelial growth factor (VEGF), only rarely increased, but if so
Macrolides (Azithromycin, Clarythromycin) Tetracycline/Doxycycline Quinolones (Ciprofloxacin, Levofloxacin) Rifampicin Ceftriaxone/Cefotaxime
Rickettsia
Pathogen: Rickettsia conorii, R. rickettsii, R. helvetica, R. slovaca, R. prowazekii (not gram- stainable, obligatory intracellular in endothelial cells)
Vector/hosts: rodents, dogs, humans, Ixodes ricinus
Symptoms: (incubation period 5 - 7 days): fever, lymphadenitis, exanthema (roseola to
Complications (app. 13%): peri-/myocarditis, renal insufficiency, pneumonia, encephalitis,
gastrointestinal bleedings, anemia, hepatitis, myalgia
- PCR on Rickettsia in blood (EDTA-blood): direct detection
Antibodies Rickettsia-IgM and -IgG: indirect detection – control of progression !
Doxycyclin/Tetracyclin Ciprofloxacin Chloramphenicol Erythromycin (Children)
Chlamydia pneumoniae
Pathogen: Chlamydophila pneumoniae (gram-negative, intracellular)
Transmission: airborne infection (aerogen), human to human, affection of epithelial cells of
Symptoms: slight throat pain, hoarseness, sinusitis, atypical pneumonia,
meningoencephalitis, bronchiolitis obliterans, myocarditis, Guillain-Barre-Syndrom
Post-infection (4-6 weeks): arthritis, tendovaginitis
Associations: e.g. Morbus Alzheimer, Multiple Sclerosis, Fibromyalgia, Chronic Fatigue
Syndrome (CFS), problems with prostate gland, heart attacks, apoplectic stroke, arteriosclerosis
- Activity test: Elispot-LTT (Lymphocytes transformation test) - PCR on chlamydia pneumoniae in sputum/secretion of the throat: direct detection - Antibodies on chlamydia pneumoniae-IgA and chlamydia pneumoniae-IgG: indirect
Macrolides (Azithromycin, Clarythromycin) Doxycycline Levofloxacin
Chlamydia trachomatis
Pathogen: Chlamydophila trachomatis (gram-negative, intracellular)
Transmission: sexual contact, human to human
Symptoms: cervicitis, sterility, urethritis, trachoma, acute conjunctivitis („swimming pool
conjunctivitis“), lymphogranuloma venereum
After infection(4-6 weeks): arthritis, tendovaginitis
- Activity determination: Elispot-LTT (Lymphocytes transformation test) - Chlamydia trachomatis PCR in urine/urogenital smear: direct detection - Antibodies on Chlamydia trachomatis-IgA and Chlamydia trachomatis-IgG: indirect
Macrolides (Azithromycin, Clarythromycin) Doxycycline Tetracycline Quinolones (Levofloxacin, Ciprofloxain, Moxifloxacin)
Mycoplasma
Pathogen: Mycoplasma pneumoniae/fermentans (gram-positive, intracellular)
Transmission: airborne infection (aerogen), human to human
Symptoms: tiredness (100%), fever, joint pain, swollen joints, muscles pain, headache,
insomnia, anxiety, emotional instability, lack of concentration, lack of alertness and memory, confusion
Risk factors: immunosuppression (e.g. AIDS), Chronic Fatigue Syndrome (CFS), „Gulf War
- Bacterial culture of special nutriment medium - PCR on chlamydia pneumoniae in sputum/secretion: direct detection - Antibodies on Mycoplasma pneumoniae-IgM, Mycoplasma pneumoniae-IgA and
Mycoplasma pneumoniae-IgG: indirect detection – control of progression !
Macrolides (Azithromycin, Clarythromycin) Doxycycline Quinolones (Levofloxacin, Ciprofloxacin)
Other possible co-infections
LI CHEN PLANUS affects around 1-2% of the population and is thought to be an auto-immune disease which can affect the skin, o ral or genital mucosa and more. The cause is unknown. U K Lichen Planus (UKLP) was set up by Bridie Nelson in November 2007 to fill the gap in support for those living with the disease Lichen Planus (LP). The group is open to members worldwide, h owever treatmen
1 0 2 2 3 S a w m i l l P k w y P o w e l l O H 4 3 0 6 5 We have reached October, our tenth month of our 12 month program of fitness. Our goal this month is to buy a new pair of shoes. A tennis shoe lasts 300-500 miles or at least twice a year get them re-placed. We have had many patients be more fit and reports of 18-32 lbs. lost, by participating in one of the many forms of lifestyle