Both of these autoimmune disorders, which cause blistering of the skin and mucous membranes, need intensive management by dermatologists in partnership with primary care physicians and other specialties, including ophthalmology and oral medicine, and disease management is often very challenging.
Previous studies of bullous pemphigoid have reported incidences between 0.2 and 3 per 100 000 person years; these are higher in older age groups, and some studies report associations with sex. In the United Kingdom, a regional study estimated an incidence of 1.4 per 100 000 person years. Wide variation in mortality is reported, with one year mortality varying between 6% in the United States and 41% in France.
In the few hospital based studies of the epidemiology of pemphigus vulgaris, the reported incidence varied between 0.076 and 1.6 per 100 000 person years. Several studies have suggested a higher incidence in women. No epidemiological data are available from the UK. Before oral corticosteroids were used, this disorder was fatal. Two hospital based studies report one year mortality of 4.8% and 54%, with no clear estimate of overall disease specific mortality.
The published studies are mainly small and hospital based; thus, although they have an excellent validity, they are unlikely to represent the full spectrum of disease. They are susceptible to selection bias, possibly leading to underestimation of incidence and overestimation of mortality. We carried out a large population based study in people with bullous pemphigoid and pemphigus vulgaris to provide robust data on incidence and demographic data in theUKand to resolve the controversies about mortality from these diseases. This study gives a more general population view of the impact of these diseases.
The health improvement network is a computerised longitudinal general practice database with demographic data similar to the general population. The version we used contained data from 328 general practices that use “In Practice Vision” software. Several studies have confirmed that the health improvement network data are sufficiently accurate for use in epidemiological research. The quality of the data has been validated against the general practice research database, a data source for more than 250 peer reviewed publications, and well confirmed disease associations have been replicated.
Between 1996 and 2006, we identified all patients with a diagnosis of bullous pemphigoid or pemphigus vulgaris from the health improvement network database. In order to exclude prevalent cases, we imposed a lag period of three months after registration with their general practitioner. This method has been previously validated by Lewis and colleagues to differentiate between incident and prevalent cases of disorders that present acutely. We selected a control group of up to four controls per case, matched randomly by age, sex and general practice. Controls also had to be alive and
contributing data to the health improvement network database on the date of diagnosis of the matched case. We excluded people aged under 20 years from both cases and controls, as both disorders are rare in this age group and may represent different diseases. We assigned a date of “pseudodiagnosis” to controls, which was the date of diagnosis for the matched case.
We recorded incident diagnoses and dates of death. The follow-up period began on the date of first
diagnosis or the date of “pseudodiagnosis” for controls.
Incidence—We calculated incidences by age, categorised into 10 year age bands; sex; and calendar
period. We used multivariate regression to model incidence rate ratios, adjusting for changes in age, sex structure, and calendar period over time. We applied calculated incidences for both diseases to the UK population totals for the years 2001-5 to estimate the number of new cases a year.
Mortality—We identified all deaths in the two case populations and matched controls and used Kaplan-
Meier techniques to calculate one yearmortality and five year survival rates. We used Cox regression to compare themortality of cases and controls, adjusting for age, sex, and calendar period.Weused Nelson-Aalen plots to test the proportional hazards assumption.
Office for National Statistics data—We calculated expected numbers of incident cases and deaths for
both diseases by applying study rates to the Office for National Statistics population (2001-5) and comparing results with Office for National Statistics data.
Sample size and power calculations—The dataset for this study contained two million person years of data. Assuming a total of 1000 cases, this study would have 90% statistical power to detect a hazard ratio for death of 2.0 or greater in cases compared with controls, at the 5% level of significance.
Our cohort included 869 people with bullous pemphigoid contributing 1993 person years and 3453 matched controls contributing 9765 person years. The median age at first presentation for bullous pemphigoid was 80 (range 23-102) years , and 534 (61%) patients were women. One hundred and thirty eight people with pemphigus vulgaris contributed 380 person years, and 551 matched controls contributed 1763 person years. The median age at first presentation for pemphigus vulgaris was 71 (21-102) years , and 91 (66%) patients were women. The median length of follow-up for people with bullous pemphigoid was 1.6 (range 0-9) years, and that for pemphigus vulgaris was 2.0 (0-10.4) years. Losses to follow-up were similar in cases and controls in both diseases (by the end of year 2, bullous pemphigoid cases and controls 34% lost; pemphigus vulgaris cases 30% lost, controls 31% lost).
The crude incidence of bullous pemphigoid was 4.28 (95% confidence interval 4.01 to 4.58) per 100 000 person years. Incidence increased with age and in later calendar periods (fig 4). The increased
incidence over calendar time persisted after adjustment for age group and sex (P for trend <0.0001). The estimated increase in the incidence of bullous pemphigoid per increase in calendar year was 17% (rate ratio 1.17, 95% confidence interval 1.14 to 1.20; P<0.0001) after adjustment for sex and age group, corresponding to a 4.8-fold increase in incidence over the 11 year period or a crude increase of 5.2-fold during the study.
As we found no association with Townsend scores and geographical regions, we excluded these from
multivariate regression.We found no evidence of effect modification to suggest that this trend was confined to a particular sex, age group, or region. Applying this data to the UK population between 2001 and 2005 gave an average of 2996 (95% confidence interval 2485 to 3602) new cases a year.
Two hundred and sixty four deaths occurred in the bullous pemphigoid cohort and 604 in the controls,
corresponding to an overall crude mortality of 131.99 (95% confidence interval 116.96 to 148.95) per 1000 person years for bullous pemphigoid and 61.86 (57.12 to 66.99) per 1000 person years for controls. The absolute excess mortality in the bullous pemphigoid cohort was 70 per 1000 person years. The one year mortality for bullous pemphigoid was 19% (95% confidence interval 16.2% to 21.8%). These data correspond to a hazard ratio of 2.11 (95% confidence interval 1.82 to 2.44). After adjustment for age, sex, and calendar period, this increased to 2.29 (1.98 to 2.65). We found no evidence of effect modification by calendar time, as the hazard ratios comparing disease cohorts with controls for each period were similar.
The crude incidence of pemphigus vulgaris was 0.68 (0.58 to 0.80) per 100 000 person years. Incidence was higher in women and in older age groups. We found evidence of an estimated 11% increase in incidence per calendar year (incidence rate ratio 1.11 (1.04 to 1.17) per year; P=0.001). We saw a slight reduction in incidence in the most recent period from 3.5 (1.9 to 6.2) in 2002-4 to 2.4 (1.2 to 4.5) in 2005-6. Applying these data to the UK population between 2001 and 2005 gave an average of 467 (297 to 643) new cases of pemphigus vulgaris a year.
Thirty six deaths occurred in the pemphigus vulgaris cohort and 58 deaths in controls, corresponding to an overall crude mortality of 94.64 (68.268 to 131.205) per 1000 person years for pemphigus vulgaris and 32.89 (25.43 to 42.55) per 1000 person years for controls. The absolute excess mortality in the
pemphigus vulgaris cohort was 62 per 1000 person years. The one year mortality for pemphigus vulgaris was 12% (8% to 19%), and the corresponding hazard ratio was 2.82 (1.86 to 4.27). We saw no deaths in cases aged less than 50 years, so we took the 50-59 year age group as the baseline group for multivariate analyses. After adjustment for sex, calendar period, and age group, the hazard ratio for death in cases increased markedly to 3.38 (2.21 to 5.17).
Comparison with Office for National Statistics Mortality Data
Applying the mortality data to the UK population data gave 1977 deaths in bullous pemphigoid cases and 221 deaths in pemphigus vulgaris cases (2001-5). These are much higher figures than the 190 and 36 deaths attributed to these diseases in the Office for National Statistics dataset.
We found a substantial increase in the incidence of both bullous pemphigoid and pemphigus vulgaris between 1996 and 2005. This increasewasnot associated with any reduction in mortality over the calendar periods and is therefore unlikely to be explained by ascertainment bias leading to the diagnosis of less severe cases. Our study therefore suggests that almost 3000 new cases of bullous
pemphigoid and 500 of pemphigus vulgaris occur each year. Age and sex adjusted mortality was more than twice as high in people with bullous pemphigoid compared with the general population and three times as high in thosewith pemphigus vulgaris. These diseases are important causes of death; the Office for National Statistics dataset reports 190 deaths from bullous pemphigoid and 36 deaths from pemphigus vulgaris between 2001 and 2005. The reported mortality for bullous pemphigoid increased from 63 to 88 per 1000 person years between 2001 and 2005, and that for pemphigus vulgaris increased from 13 to 19 per 1000 person years. Applying themortalitydata fromour study to the Office for National Statistics population gives a much higher estimate of 2198 deaths between both diseases in the UK between 2001 and 2005, although we did not measure the underlying cause of death.
Strengths and weaknesses
This is a large, population based study, which allows robust estimation of incidence and mortality. This is less susceptible to selection bias than other study designs and allows prospective study of disease trends over time. The size of the dataset gives sufficient power to exclude chance as the basis for the findings. The use of routinely collected data means that we could not validate the diagnoses or assess severity of disease. These diagnoses are made in secondary care, usually with skin biopsies and immunofluorescent techniques to confirm the clinical diagnosis; they are therefore likely to be accurate. Both bullous pemphigoid and pemphigus vulgaris are uncommonly seen in general practice, and general practitioners are highly unlikely to record these diagnoses without referring to secondary or tertiary care. The potentially catastrophic consequences of giving corticosteroids or other immunosuppressants to people with infective causes of blistering mean that appropriate investigations are very likely to be carried out in secondary or tertiary care to confirm the diagnosis. We were also able to confirm that 94% of our cases were being treated with either oral or potent topical corticosteroids or a relevant steroid sparing agent after diagnosis or had evidence of referral to hospital, which further supports the validity of the diagnoses. Previous studies of other conditions have confirmed the validity of diagnoses in both the general practice research database and the health improvement network. Limiting the dataset to practices considered “up to standard” will have improved the quality of data, as retrospective collection and coding of data is no longer a problem. Some of the cases included may be prevalent rather than incident cases, however. If this is the case, the results may be affected by survival bias and we may have underestimated the mortality associated with these diseases; so the true mortality may be even higher.
Comparison with other studies
The mean age of patients with bullous pemphigoid in our study is similar to other published data. However, with the exception of one regional study, all studies were hospital based; therefore, although theymayhave had excellent validity, they may be less representative of the disease in the population. The mean age of patients with pemphigus vulgaris in our study was much higher than previous reports. However, no data on the epidemiology of pemphigus vulgaris in western Europe have been published and all of the studies are from hospital centres in the form of either cross sectional surveys or case series; these studies are unlikely to give reliable population based statistics.
The incidence of bullous pemphigoid in our study is similar to that described by Garcia-Doval and colleagues3; the incidence of pemphigus vulgaris is within the range of the previous papers, and the sex distribution is also similar.91012 The increasing trend in incidence of bullous pemphigoid has not been previously shown, but no study has looked at incidence of bullous pemphigoid prospectively over time. A possible explanation is increased ascertainment, but if this is the case the increasing trend has not levelled off. The number of consultant dermatologists in the UK increased by 39% between 1998 and 2006. This may have contributed to increased ascertainment but is unlikely to explain completely the increased incidence because of the acute, severe presentations of these disorders.
One year mortality from bullous pemphigoid is lower (19%) than previously described in studies from Europe (25-41%) but is intermediate between those described in the United States (11%) and Europe. Non-inclusion of patients in nursing homes is not a likely explanation for this as almost all patients in nursing homes are under the care of general practitioners. Despite recent published literature showing the similar efficacy of potent topical steroids and oral corticosteroids for bullous pemphigoid, oral corticosteroids remain in widespread use and may therefore contribute to high mortality.19 One year mortality for pemphigus vulgaris is higher than that described in a recent study of younger cases in Turkey (4.8%) but lower than that described in a study from the United States by Ryan and colleagues in 1971 (54%; mean age of cases not given). The designs used in both of these studies are highly susceptible to selection bias, and drawing any robust conclusions from the findings is difficult.
Interpretation and implications
Ourstudy shows that rates of bullous pemphigoid seem to be increasing over time. Rates of pemphigus vulgaris are increasing to a lesser degree despite the facts that both disorders are more common with increasing age and that the multivariate analysis was adjusted for age. Possible explanations include ascertainment bias, misclassification, and a true increase in incidence. If the last of these is true, further investigation is warranted into the reasons for this, as it may provide further insight into the causes of the disorders. The lack of a socioeconomic gradient and major geographical variation argues against the environment playing an important role in causing the diseases.
Our study has shown high mortality associated with these diseases; rates were twice that in the general population in patients with bullous pemphigoid and three times as high as in the general population in those with pemphigus vulgaris. With the increasing age of our population, the morbidity and mortality from these diseases will increase. Previous measures have underestimated the burden of these diseases, in terms of both incidence and risk of death.