Nutritional supplements that may be helpful: Low blood levels
of the hormone DHEA and the related compound DHEA-sulfate have been associated with more
severe symptoms in people with SLE.26 Preliminary trials have suggested that 50 to
200 mg per day DHEA improved symptoms in people with SLE.27 28 One
double-blind trial of women with mild to moderate SLE found that 200 mg of DHEA per day improved symptoms and allowed a greater decrease in prednisone use,29 but a similar trial
in women with severe SLE found only insignificant benefits.30
Experts have concerns about the use of DHEA, particularly
because there are no long-term safety data . Side effects at high intakes (50 to 200 mg per
day) in one 12-month trial included acne (in over 50% of people), increased facial hair (18%),
and increased perspiration (8%). Less common problems reported with DHEA supplementation were
breast tenderness, weight gain, mood alteration, headache, oily skin, and menstrual
irregularity.31
High amounts of DHEA have caused cancer in animals.32 33 Although
anticancer effects of DHEA have also been reported,34 they involve trials
using animals that do not process DHEA the way humans do, so these positive effects may have
no relevance for people. Links have begun to appear between higher DHEA levels and risks of
prostate cancer in humans.35 At least one person with prostate cancer has been reported to have had a worsening
of his cancer despite feeling better while taking very high amounts (up to 700 mg per day) of
DHEA.36 While younger women with breast cancer may have low levels of DHEA,
postmenopausal women with breast cancer appear to
have high levels of DHEA, which has researchers concerned.37 These cancer concerns
make sense because DHEA is a precursor to testosterone (linked to prostate cancer) and
estrogen (linked to breast cancer). Until more is known, it would be prudent for people with
breast or prostate cancer or a family history of these conditions to avoid supplementing with
DHEA. Preliminary evidence has also linked higher DHEA levels to ovarian cancer in
women.38
Some doctors recommend that people taking DHEA have liver enzymes measured routinely.
Anecdotes of DHEA supplementation (of at least 25 mg per day) leading to heart arrhythmias have appeared.39 At only
25 mg per day, DHEA has lowered HDL cholesterol while increasing insulin-like growth factor
(IGF).40 Decreasing HDL could increase the risk of heart disease. Increasing IGF might increase the
risk of breast cancer.
The omega-3 fatty acids in fish
oil—eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA)—decrease inflammation. Supplementation with EPA and DHA has
prevented autoimmune lupus in animal research.41 In a double-blind trial, 20 grams
of fish oil daily combined with a low-fat diet led to
improvement in 14 of 17 people with SLE in 12 weeks.42 Smaller amounts of fish oil
have led to only temporary improvement in another double-blind trial.43 People
wishing to take such a large amount of fish oil should first consult with a doctor.
Antioxidant levels have been reported to be low in
people with SLE, though this finding was not statistically significant in one
trial.44 When animals are fed antioxidant-deficient diets, they develop a condition
similar to SLE; supplementation with antioxidants, such as
vitamin C, vitamin E, beta-carotene, and
selenium, has helped animals with existing SLE.45 It remains unclear whether
antioxidant supplementation would have a positive effect on people with SLE.
Some preliminary evidence suggests that vitamin E might
help people with discoid lupus erythematosus (DLE). Two doctors reported good to excellent
results by giving 800–2,000 IU of vitamin E per day to eight people with
DLE.46 47 According to these physicians, lower amounts of vitamin E did
not work as well. In another small trial, vitamin E, also given in high amounts, had no
effect.48 Unlike with DLE, there appear to be no reports on the effects of vitamin
E in people with SLE.
In one preliminary report, 250,000 IU beta-carotene per day cleared up all facial rashes in
as little as one week for three people with DLE.49 However, another study involving
26 people (19 with DLE and seven with SLE) found that using an even higher intake (400,000 IU
per day) for an average of five and a half months was ineffective.50 Research has
not yet supported the use of beta-carotene for people with SLE.
Preliminary research suggests that pantothenic acid,
when taken together with vitamin E, may help those with DLE. In one trial, taking 10 to 15
grams of pantothenic acid per day with 1,500 to 3,000 IU of vitamin E per day for as long as
19 months, helped 67 people with DLE.51 Pantothenic acid by itself for shorter
periods of time in lower amounts has been reported to fail.52 The amounts of
pantothenic acid and vitamin E used in the first trial are very high and should not be taken
without the supervision of a physician.
Are there any side effects or interactions? Refer to the individual supplement for
information about any side effects or interactions.
References:
1. Kardestuncer T, Frumkin H. Systemic lupus erythematosus in relation to
environmental pollution: an investigation in an African-American community in North Georgia.
Arch Environ Health 1997;52:85–90.
2. Fjellner B. Drug-induced lupus erythematosus aggravated by oral
therapy. Acta Derm Venereol 1979;59:368–70.
3. Millard TP, Hawk JL, McGregor JM. Photosensitivity in lupus.
Lupus 2000;9:3–10 [review].
4. Reidenberg MM, Durant PJ, Harris RA, et al. Lupus erythematosus-like
disease due to hydrazine. Am J Med 1983;75:365–70.
5. Pereyo N. Hydrazine derivatives and induction of systemic lupus
erythematosus. J Am Acad Dermatol 1986;14:514–5 [letter].
6. Nagata C, Fuyita, Iwata H, et al. Systemic lupus erythematosus: a
case-control epidemiologic study in Japan. Int J Dermatol 1995;34:333–7.
7. Minami Y, Sasaki Ti, Komatsu S, et al. Female systemic lupus
erythematosus in Miyagi Prefecture, Japan: a case-control study of dietary and reproductive
factors. Tohoku J Exp Med 1993;169:245–52.
8. Nagata C, Fuyita, Iwata H, et al. Systemic lupus erythematosus: a
case-control epidemiologic study in Japan. Int J Dermatol 1995;34:333–7.
9. Kardestuncer T, Frumkin H. Systemic lupus erythematosus in relation to
environmental pollution: an investigation in an African-American community in North Georgia.
Arch Environ Health 1997;52:85–90.
10. Comstock GW, Burke AE, Hoffman SC, et al. Serum concentrations of
alpha-tocopherol, beta-carotene, and retinol preceding the diagnosis of rheumatoid arthritis
and systemic lupus erythematosus. Ann Rheum Dis 1997;56:323–35.
11. Nagata C, Fuyita, Iwata H, et al. Systemic lupus erythematosus: a
case-control epidemiologic study in Japan. Int J Dermatol 1995;34:333–7.
12. Shigemasa C, Tanaka T, Mashiba H. Effect of vegetarian diet on
systemic lupus erythematosus. Lancet 1992;339:1177 [letter].
13. Minami Y, Sasaki Ti, Komatsu S, et al. Female systemic lupus
erythematosus in Miyagi Prefecture, Japan: a case-control study of dietary and reproductive
factors. Tohoku J Exp Med 1993;169:245–52.
14. Corman LC. The role of diet in animal models of systemic lupus
erythematosus: possible implications for human lupus. Semin Arthritis Rheum
1985;15:61–9 [review].
15. Clark WF, Parbtani A, Huff MW, et al. Flaxseed: a potential treatment
for lupus nephritis. Kidney Int 1995;48:475–80.
16. Prasad K. Hydroxyl radical-scavenging property of
secoisolariciresinol diglucoside (SDG) isolated from flax-seed. Mol Cell Biochem
1997;168:117–23.
17. Diumenjo MS, Lisanti M, Valles R, Rivero I. Allergic manifestations
of systemic lupus erythematosus. Allergol Immunopathol (Madr) 1985;13:323–6 [in
Spanish].
18. Nagata C, Fuyita, Iwata H, et al. Systemic lupus erythematosus: a
case-control epidemiologic study in Japan. Int J Dermatol 1995;34:333–7.
19. Carr RI, Tilley D, Forsyth S, et al. Failure of oral tolerance in
(NZB X NZW)F1 mice is antigen specific and appears to parallel antibody patterns in human
systemic lupus erythematosus (SLE). Clin Immunol Immunopathol
1987;42:298–310.
20. Rutkowska-Sak L, Legatowicz-Koprowska M, Ryzko J, Socha J. Changes in
the gastrointestinal system of children with inflammatory systemic connective tissue diseases.
Pediatr Pol 1995;70:235–41 [in Polish].
21. Carr R, Forsyth S, Sadi D. Abnormal responses to ingested substances
in murine systemic lupus erythematosus: apparent effect of a casein-free diet on the
development of systemic lupus erythematosus in NZB/W mice. J Rheumatol 1987;14 (suppl
13):158–65.
22. Bardana EJ Jr, Malinow MR, Houghton DC, et al. Diet-induced systemic
lupus erythematosus (SLE) in primates. Am J Kidney Dis 1982;1:345–52.
23. Roberts JL, Hayashi JA. Exacerbation of SLE associated with alfalfa
ingestion. N Engl J Med 1983;308(22):1361 [letter].
24. Malinow MR, McLaughlin P, Bardana EJ Jr, Craig S. Elimination of
toxicity from diets containing alfalfa seeds. Food Chem Toxicol
1984;22:583–7.
25. Hardy CJ, Palmer BP, Muir KR, et al. Smoking history, alcohol
consumption, and systemic lupus erythematosus: a case-control study. Ann Rheum Dis
1998;57:451–5.
26. Barry NN, McGuire JL, van Vollenhoven RF. Dehydroepiandrosterone in
systemic lupus erythematosus: relationship between dosage, serum levels, and clinical
response. J Rheumatol 1998;25:2352–6.
27. Van Vollenhoven RF, Morabito LM, Engleman EG, McGuire JL. Treatment
of systemic lupus erythematosus with dehyroepiandrosterone: 50 patients treated up to 12
months. J Rheumatol 1998;25:285–9.
28. Van Vollenhoven RF, Engleman EG, McGuire JL. An open study of
dehydroepiandrosterone in systemic lupus erythematosus. Arthritis Rheum
1994;37:1305–10.
29. Van Vollenhoven RF, Engleman EG, McGuire JL. Dehydroepiandrosterone
in systemic lupus erythematosus. Results of a double-blind, placebo-controlled, randomized
clinical trial. Arthritis Rheum 1995;38:1826–31.
30. Van Vollenhoven RF, Park JL, Genovese MC, et al. A double-blind,
placebo-controlled, clinical trial of dehydroepiandrosterone in severe systemic lupus
erythematosus. Lupus 1999;8:181–7.
31. van Hollenhoven RF, Morabito LM, Engleman EG, McGuire JL. Treatment
of systemic lupus erythematosus with dehydroepiandrosterone: 50 patients treated up to 12
months. J Rheumatol 1998;25:285–9.
32. Orner GA, Mathews C, Hendricks JD, et al. Dehydroepiandrosterone is a
complete hepatocarcinogen and potent tumor promoter in the absence of peroxisome proliferation
in rainbow trout. Carcinogenesis 1995;16:2893–8.
33. Metzger C, Mayer D, Hoffmann H, et al. Sequential appearance and
ultrastructure of amphophilic cell foci, adenomas, and carcinomas in the liver of male and
female rats treated with dehydroepiandrosterone. Taxicol Pathol
1995;23:591–605.
34. Schwartz AG. Inhibition of spontaneous breast cancer formation in
female C3H (A vy/a) mice by long-term treatment with dehydroepiandrosterone. Cancer
Res 1979;39:1129–32.
35. McNeil C. Potential drug DHEA hits snags on way to clinic. J Natl
Cancer Inst 1997;89:681–3.
36. Jones JA, Nguyen A, Strab M, et al. Use of DHEA in a patient with
advanced prostate cancer: a case report and review. Urology 1997;50:784–8.
37. Zumoff B, Levin J, Rosenfeld RS, et al. Abnormal 24-hr mean plasma
concentrations of dehydroisoandrosterone and dehydroisoandrosterone sulfate in women with
primary operable breast cancer. Cancer Res 1981;41:3360–3.
38. Skolnick AA. Scientific verdict still out on DHEA. JAMA
1996;276:1365–7 [review].
39. Sahelian R. New supplements and unknown, long-term consequences.
Am J Natural Med 1997;4:8 [editorial].
40. Casson PR, Santoro N, Elkind-Hirsch K, et al. Postmenopausal
dehydroepiandrosterone administration increases free insulin-like growth factor-I and
decreases high-density lipoprotein: a six-month trial. Fertil Steril
1998;70:107–10.
41. Kelley VE, Ferretti A, Izui S, Strom TB. A fish oil diet rich in
eicosapentaenoic acid reduces cyclooxygenase metabolites, and suppresses lupus in MRL-1pr
mice. J Immunol 1985;134:2914–9.
42. Walton AJE, Snaith ML, Locniskar M, et al. Dietary fish oil and the
severity of symptoms in patients with systemic lupus erythematosus. Ann Rheum Dis
1991;50:463–6.
43. Westberg G, Tarkowski A. Effect of MaxEPA in patients with SLE.
Scand J Rheumatology 1990;19:137–43.
44. Comstock GW, Burke AE, Hoffman SC, et al. Serum concentrations of
alpha-tocopherol, beta-carotene, and retinol preceding the diagnosis of rheumatoid arthritis
and systemic lupus erythematosus. Ann Rheum Dis 1997;56:323–35.
45. Weimann BJ, Weiser H. Effects of antioxidant vitamins C, E, and
beta-carotene on immune functions in MRL/lpr mice and rats. Ann N Y Acad Sci
1992;669:390–2.
46. Ayres S Jr, Mihan R. Is vitamin E involved in the autoimmune
mechanism? Cutis 1978;21:321–5.
47. Ayres S Jr, Mihan R. Lupus erythematosus and vitamin E: an effective
and nontoxic therapy. Cutis 1979;23:49–54.
48. Yell JA, Burge S, Wojnarowska F. Vitamin E and discoid lupus
erythematosus. Lupus 1992;1:303–5.
49. Newbold PC. Beta-carotene in the treatment of discoid lupus
erythematosus. Br J Dermatol 1976;95:100–1.
50. Dubois EL, Patterson C. Ineffectiveness of beta-carotene in lupus
erythematosus JAMA 1976;236:138–9 [letter].
51. Welsh AL. Lupus erythematosus: Treatment by combined use of massive
amounts of pantothenic acid and vitamin E. Arch Dermatol Syphilol
1954;70:181–98.
52. Cochrane T, Leslie G. The treatment of lupus erythematosus with
calcium pantothenate and panthenol. J Invest Dermatol 1952;18:365–7.
53. Wang ZY. Clinical and laboratory studies of the effect of an
antilupus pill on systemic lupus erythematosus. Chung His I Chieh Ho Tsa Chih
1989;9:452,465–8 [in Chinese].
54. Ruan J, Ye RG. Lupus nephritis treated with impact therapy of
cyclophosphamide and traditional Chinese medicine. Chung Kuo Chung His I Chieh Ho Tsa
Chih 1994;14:260, 276–8 [in Chinese].
55. Chen JR, Yen JH, Lin CC, et al. The effects of Chinese herbs on
improving survival and inhibiting anti-ds DNA antibody production in lupus mice. Am J Chin
Med 1993;21:257–62.
56. Wanzhang Q. Clinical observations on Tripterygium wilfordii
in the treatment of 26 cases of discoid lupus erythematosus. J Trad Chin Med
1983;3:131–2.
57. Wanzhang Q. Tripterygium wilfordii hook F. in systemic lupus
erythematosus. Report of 103 cases. Chin Med J 1981;94:827–34.
58. Chou WC, Wu CC, Yang PC, Lee YT. Hypovolemic shock and mortality
after ingestion of Tripterygium wilfordii hook F: a case report. Int J
Cardiol 1995;49:173–7.
59. Huang L, Feng S, Wang H. Decreased bone mineral density in female
patients with systemic lupus erythematosus after long-term administration of Tripterygium
wilfordii Hook. F. Chinese Med J 2000;113:159–61.
60. Klepser T, Nisly N. Astragalus as an adjunctive therapy in
immunocompromised patients. Alt Med Alert 1999;Nov:125–8 [review].