| Literature DB >> 21423581 |
Adriane Fugh-Berman1, Christina Pike McDonald, Alicia M Bell, Emily Catherine Bethards, Anthony R Scialli.
Abstract
BACKGROUND: Even after the Women's Health Initiative (WHI) found that the risks of menopausal hormone therapy (hormone therapy) outweighed benefit for asymptomatic women, about half of gynecologists in the United States continued to believe that hormones benefited women's health. The pharmaceutical industry has supported publication of articles in medical journals for marketing purposes. It is unknown whether author relationships with industry affect promotional tone in articles on hormone therapy. The goal of this study was to determine whether promotional tone could be identified in narrative review articles regarding menopausal hormone therapy and whether articles identified as promotional were more likely to have been authored by those with conflicts of interest with manufacturers of menopausal hormone therapy. METHODS ANDEntities:
Mesh:
Year: 2011 PMID: 21423581 PMCID: PMC3058057 DOI: 10.1371/journal.pmed.1000425
Source DB: PubMed Journal: PLoS Med ISSN: 1549-1277 Impact factor: 11.069
Scientific accuracy and promotional tone in articles on menopausal hormone therapy.
| Articles authored or coauthored by authors with potential financial conflicts of interest | Articles authored or coauthored by authors without potential financial conflicts of interest | ||
| Scientific accuracy | No | 6 | 1 |
| Yes | 35 | 8 | |
| Promotional tone | No | 11 | 7 |
| Yes | 30 | 2 |
Authors with potential financial conflicts of interest: Leon Speroff, Thomas B. Clarkson, Peter Kenemans, Rogerio A. Lobo, David M. Herrington, Marius J. van der Mooren, Rowan T. Chlebowski, Susan R. Davis.
Authors with no evidence of potential financial conflicts of interest: Nanette K. Wenger, Nananda F. Col.
The following footnotes indicate references listed in Text S1.
A10, A12, A25, A29, A35, A45.
A4.
A1-2, A5, A8-9, A11, A14, A15-24, A26-27, A30-34, A36-38, A40-43, A46-48, A50.
A3, A6-7, A13, A28, A39, A44, A49.
A1-2, A16-17, A22, A24-25, A32, A46, A47-48.
A6-7, A13, A28, A39, A44, A49.
A5, A8, A9-12, A14-15, A18-21, A23, A26-27, A29-31, A33-38, A40-43, A45, A50.
A3, A4.
Themes consistently identified in promotional articles, with examples.
| Theme | Examples |
| The Women's Health Initiative was flawed. | “Will postmenopausal hormone therapy begun at or near the time of the menopause, and maintained for a relatively long duration of time, provide protection against coronary artery disease (primary prevention)? The design of the canceled arm of the WHI did not allow an answer to this question.” (A10, A50) |
| The Women's Health Initiative was a controversial trial. | “The proper role of hormone replacement therapy (HRT) for the treatment and prevention of cardiovascular disease remains a controversial and heavily debated topic.” (A32)“… we cannot formulate any general advice that holds for the majority of European post-menopausal women due to lack of consistency, lack of biological plausibility, and lack of relevance of randomized clinical trial data to our daily practical work.” (A11)“Therefore, the WHI results are questionable and uncertain even if obtained in a gold standard randomized clinical trial, and for sure these data cannot be extrapolated to the younger and healthier perimenopausal women.” (A35) |
| The population studied in the Women's Health Initiative was inappropriate or was not representative of the general population of menopausal women. | “In the three large RCTs available, the populations studied are: not representative, too old and without climacteric complaints, and therefore lacking any indication for postmenopausal hormone therapy (HT).” (A11)“Randomized controlled trials are very powerful investigative tools that are, by design, limited in their interpretation to populations covered by the randomized controlled trial.” (A43) |
| Clinical trial results should not guide treatment for individuals. | “To do as the editorialists recommend (to categorically discourage the use of hormone therapy) is to deny women the assistance they need to make individual decisions based upon individual characteristics and needs.” (A8) |
| Observational studies are as good or better than randomized clinical trials. | “However, a truly randomized, placebo-controlled, HT trial in women entering menopause is very difficult or even impossible to carry out in practice and observational studies are more akin to the approach of physicians in clinical practice.” (A31) |
| Animal studies can guide clinical decision-making. | “There is strong evidence that ET/HT provides cardioprotection in primary prevention studies of animal models with supportive data from studies of women in the EPAT and Nurses' Health Study.” (A27) |
| The risks associated with hormone therapy have been exaggerated. | “The important unanswered question is whether hormone therapy causes breast cancer or is promoting the diagnosis of pre-existing tumors.” (A8)“It is also worth pointing out that the reported risk with hormone therapy is even smaller than that associated with recognized risk factors such as a positive family history, being overweight after menopause, and alcohol intake.” (A10, A30, A50)“However, this proportion was not due to an epidemic of breast cancer in the HRT group but rather to an unexplained decreased incidence of breast cancer cases in the placebo group.” |
| The benefits of hormone therapy have been or will be proven; recent studies are an aberration. | “Mortality from all causes is lower in HRT users compared with non-users.” (A12)“However, even after the most contemporary and careful attempts to adjust for possible confounders, HRT use continues to be associated with more favorable outcomes.” (A15)“With many observational trials indicating a cardioprotective effect of early estrogen treatment and the absence of a prospective, randomized clinical trial powered to reveal cardioprotection starting during the menopausal transition it seems prudent not to dismiss such an effect.” (A43)“There continues to be good reason to believe that there are benefits associated with treatment, including improvement of quality of life beyond the relief of hot flushes, maximal protection against osteoporotic fractures, a reduction in colorectal cancers, maintenance of skin turgor and elasticity, and the possibility of primary prevention of CHD and Alzheimer's disease.” (A10) |
See Text S1 for referenced articles given in parenthesis.
Examples of language promoting or not promoting the use of hormone therapy.
| Promotional | Nonpromotional |
| “…the WHI did not study the appropriate population in the appropriate time period to establish that hormone therapy does not exert a primary preventive effect on the risk of CHD.” (A10, A50) | “The role of conventional HRT for treatment and prevention of CHD is rapidly evolving from presumed benefit to proven harm.” (A46) |
| “Are such experts jumping to conclusions, and jeopardizing the health and quality of life of these peri- and early postmenopausal women, who differ from those in the WHI trial, two-thirds of whom were over 60 years old?” (A18) | “…use of menopausal hormone therapy (MHT) for chronic disease risk reduction in any population cannot be supported.” (A47) |
| “Wherever we live we are surrounded by risks, sometimes not known to us. Air and water pollution, various forms of radiation, insecticides in food and road accidents are good examples. Do we stop using the car? Certainly not! We take the small risk because of the benefits.” (A35) | “Although the majority of WHI women had no adverse events, the population risk is substantial, such that the global risk: benefit profile does not warrant recommendation of this therapy as a widespread preventive intervention.” (A7) |
| “Given the practical challenges in conducting randomized controlled trials to compare the various estrogens, drawing inferences from valid observational studies seems the only realistic alternative.” (A3) | “Observational studies have inherent biases that cannot be corrected for; therefore evidence should come from randomized clinical trials (RCTs).” (A11) |
| “The use of animal models allows for the evaluation of direct breast cancer effects of ET [estrogen therapy] and HT and avoids some of the confounding variables that are necessarily a part of studies on postmenopausal women.” (A38) | “…observational or mechanistic studies, animal models, and basic research have tremendous value for the generation of hypotheses but should not be used to justify broad-based pharmacologic interventions.” (A5) |
See Text S1 for referenced articles given in parenthesis.