Silver birch

Related Terms

Bet v 1, Bet v 1-fragments, Bet v 1-trimer, Betula, Betula 30c, Betula davurica Pall., Betula ermanii Cham., Betula grossa Sieb. et Zucc., Betula maximowicziana, Betula maximowicziana Regel, Betula nana, Betula nana L., Betula occidentalis, Betula pendula, Betula pendula Roth., Betula papyrifera Marsh., Betula platyphylla var. japonica, Betula platyphylla Sukatchev var. japonica (Miq.) Hara, Betula pubescens Ehrh., Betula verrucosa, Betulaceae (family), betulin, betulinic acid, birch pollen allergen (Bet v 1), downy birch, dwarf birch, Japanese white birch, lupeol, mountain birch, natural birch pollen extract, oleanolic acid, paper birch, rBet v 1, rBet v 2, rBet v 4, recombinant Betula verrucosa (rBet v 1), silver birch, white birch.
Note: This monograph does not cover birch immunotherapy. For more information on immunotherapy, please see the Natural Standard allergy database.

Background

Birch tree species are common throughout temperate North American, European, and Asian areas. Birch pollen is one of the most common allergens, usually in areas where exposure to high levels of birch pollen is common. The allergen may cause atopic dermatitis, contact urticaria (hives), atopic eczema, asthma, wheezing, allergic conjunctivitis (pinkeye), eye redness, oral-pharyngeal itching, or rhinoconjunctivitis (inflammation of the lining of the nose and the mucous membrane that covers the front of the eye and lines the eyelids).
There is insufficient evidence in humans to support the use of birch for any indication. One study shows that birch bark ointment may be beneficial for actinic keratosis (precancerous condition of thick, scaly patches of skin).

Evidence Table

These uses have been tested in humans or animals. Safety and effectiveness have not always been proven. Some of these conditions are potentially serious, and should be evaluated by a qualified healthcare provider. GRADE *
These uses have been tested in humans or animals. Safety and effectiveness have not always been proven. Some of these conditions are potentially serious, and should be evaluated by a qualified healthcare provider. GRADE *


Birch bark contains a variety of apoptosis (cell death)-inducing and anti-inflammatory substances such as betulinic acid, betulin, oleanolic acid, and lupeol, which may be beneficial in treating actinic keratosis. More study is needed in this area.

C


Birch bark contains a variety of apoptosis (cell death)-inducing and anti-inflammatory substances such as betulinic acid, betulin, oleanolic acid, and lupeol, which may be beneficial in treating actinic keratosis. More study is needed in this area.

C
* Key to grades

A: Strong scientific evidence for this use
B: Good scientific evidence for this use
C: Unclear scientific evidence for this use
D: Fair scientific evidence for this use (it may not work)
F: Strong scientific evidence against this use (it likley does not work)
* Key to grades

A: Strong scientific evidence for this use
B: Good scientific evidence for this use
C: Unclear scientific evidence for this use
D: Fair scientific evidence for this use (it may not work)
F: Strong scientific evidence against this use (it likley does not work)

Tradition / Theory

The below uses are based on tradition, scientific theories, or limited research. They often have not been thoroughly tested in humans, and safety and effectiveness have not always been proven. Some of these conditions are potentially serious, and should be evaluated by a qualified healthcare provider. There may be other proposed uses that are not listed below.

Dosing

Adults (18 years and older):
IMPORTANT NOTE: Patients with allergies should not self-treat. Supervision by a trained Allergist is crucial due to the risk for serious, even life-threatening, effects. There is no proven safe or effective dose for birch.

Safety

The U.S. Food and Drug Administration does not strictly regulate herbs and supplements. There is no guarantee of strength, purity or safety of products, and effects may vary. You should always read product labels. If you have a medical condition, or are taking other drugs, herbs, or supplements, you should speak with a qualified healthcare provider before starting a new therapy. Consult a healthcare provider immediately if you experience side effects.

Interactions

Interactions with Drugs
Birch may interact with blood thinning agents. Caution is advised in patients with bleeding disorders or taking agents that may increase the risk of bleeding. Dosing adjustments may be necessary.
Birch may have diuretic (increase urine production) effects. Caution is advised in patients taking agents that increase the flow of urine.
Birch may be hepatotoxic (liver damaging). Caution is advised in patients with liver disorders or taking drugs that may affect the liver.

Attribution

This information is based on a systematic review of scientific literature edited and peer-reviewed by contributors to the Natural Standard Research Collaboration (www.naturalstandard.com).

Bibliography

Arvidsson MB, Lowhagen O, Rak S. Allergen specific immunotherapy attenuates early and late phase reactions in lower airways of birch pollen asthmatic patients: a double blind placebo-controlled study. Allergy 2004;59(1):74-80.
Bez C, Schubert R, Kopp M, et al. Effect of anti-immunoglobulin E on nasal inflammation in patients with seasonal allergic rhinoconjunctivitis. Clin Exp Allergy 2004;34(7):1079-1085.
Bist A, Kumar L, Roy I, et al. Clinico-immunologic evaluation of allergy to Himalayan tree pollen in atopic subjects in India--a new record. Asian Pac J Allergy Immunol 2005;23(2-3):69-78.
Bolhaar ST, Tiemessen MM, Zuidmeer L, et al. C. Efficacy of birch-pollen immunotherapy on cross-reactive food allergy confirmed by skin tests and double-blind food challenges. Clin Exp Allergy 2004;34(5):761-769.
Bolhaar ST, Zuidmeer L, Ma Y, et al. A mutant of the major apple allergen, Mal d 1, demonstrating hypo-allergenicity in the target organ by double-blind placebo-controlled food challenge. Clin Exp Allergy 2005;35(12):1638-1644.
Cirla AM, Cirla PE, Parmiani S, et al. A pre-seasonal birch/hazel sublingual immunotherapy can improve the outcome of grass pollen injective treatment in bisensitized individuals. A case-referent, two-year controlled study. Allergol Immunopathol (Madr.) 2003;31(1):31-43.
Hansen KS, Khinchi MS, Skov PS, et al. Food allergy to apple and specific immunotherapy with birch pollen. Mol Nutr Food Res 2004;48(6):441-448.
Huyke C, Laszczyk M, Scheffler A, et al. [Treatment of actinic keratoses with birch bark extract: a pilot study]. J Dtsch Dermatol Ges 2006;4(2):132-136.
Khinchi M S, Poulsen LK, Carat F, et al. Clinical efficacy of sublingual and subcutaneous birch pollen allergen-specific immunotherapy: a randomized, placebo-controlled, double-blind, double-dummy study. Allergy 2004;59(1):45-53.
Marogna M, Spadolini I, Massolo A, et al. Clinical, functional, and immunologic effects of sublingual immunotherapy in birch pollinosis: a 3-year randomized controlled study. J Allergy Clin Immunol 2005;115(6):1184-1188.
Mittag D, Akkerdaas J, Ballmer-Weber BK, et al. Ara h 8, a Bet v 1-homologous allergen from peanut, is a major allergen in patients with combined birch pollen and peanut allergy. J.Allergy Clin Immunol 2004;114(6):1410-1417.
Mosges R, Pasch N, Schlierenkamper U, et al. Comparison of the biological activity of the most common sublingual allergen solutions made by two European manufacturers. Int Arch Allergy Immunol 2006;139(4):325-329.
Niederberger V, Horak F, Vrtala S, et al. Vaccination with genetically engineered allergens prevents progression of allergic disease. Proc Natl Acad Sci USA 10-5-2004;101 Suppl 2:14677-14682.
Reisinger J, Horak F, Pauli G, et al. Allergen-specific nasal IgG antibodies induced by vaccination with genetically modified allergens are associated with reduced nasal allergen sensitivity. J Allergy Clin Immunol 2005;116(2):347-354.
van Neerven RJ, Arvidsson M, Ipsen H, et al. A double-blind, placebo-controlled birch allergy vaccination study: inhibition of CD23-mediated serum-immunoglobulin E-facilitated allergen presentation. Clin Exp Allergy 2004;34(3):420-428.