Archives

  • 2018-07
  • 2018-10
  • 2018-11
  • 2019-04
  • 2019-05
  • 2019-06
  • 2019-07
  • 2019-08
  • 2019-09
  • 2019-10
  • 2019-11
  • 2019-12
  • 2020-01
  • 2020-02
  • 2020-03
  • br A hundred years after

    2018-10-25


    A hundred years after its description in 1917 by John Lindberg, a Finnish ophthalmologist () pseudoexfoliation syndrome (PES) — an eye abnormality estimated to affect 80 million people and to be associated with a significantly increased risk of cataract and secondary open-angle glaucoma, both of which may compromise vision — continues to be shrouded in mysteries (). Why is PES so often unilateral? Why does not everyone with PES develop secondary glaucoma? Why do lysyl oxidase like-1 gene polymorphisms that are strongly associated with PES () vary in different populations ()? What actually is the pseudoexfoliation material, visible in the eye by biomicroscopy and elsewhere in the body by electron microscopy? Is it identical inside and outside of the eye ()? Finally, and perhaps most importantly, is PES a systemic disease that shortens life expectancy? This is what from Norway, a country with a long tradition of PES research, address in this issue of EBioMedicine. The authors conducted in 1985–1986 an epidemiological survey covering 1888 of the 2109 inhabitants older than 64years in three Norwegian municipalities and determined by biomicroscopy whether they were PES-positive (). They returned to this cohort in 2014 by which time 99% of their subjects had died, and requested their dates of death (). The authors found no difference in all-cause mortality: the relative risk of death for PES-positive subjects, adjusting for gender and age, was 1.01 and the median life spans of PES-positive and PES-negative subjects were similar in all age groups studied. These long-term, population-based data corroborate half a dozen cohort studies conducted previously albeit typically with shorter, less mature follow-up — the Act 1 of addressing the potentially different life spans of PES-positive subjects (for references see ). As the authors point out, their results are also inconsistent with studies that have reported impaired circulation in vital organs such as the aorta, heart and transcription factors as well as potentially deleterious hyperhomocystinemia in PES-positive subjects (for references see ). Such claims have independently been challenged by data from other centers, which also has spoken against a clinically significant, true association between PES, vascular disease and, indirectly, excess mortality (). Although one tends to agree with the main conclusion of in that PES is unlikely to be a life threatening condition — an important message to millions of people — one has to address potential bias in their statistics. A notable confounding factor that the authors mention — and one that Restriction Enzyme cannot adjust for — is that although several PES-negative subjects most likely later converted to PES-positive ones they were still all counted as PES-negative. One can roughly estimate the magnitude of this bias as follows. First, the prevalence of PES by age group given in Table 1 of can be plotted to provide prevalence estimates for other ages (). Second, the eventual median age of PES-negative subjects by age group can be read from Fig. 1 of . One can then read the corresponding predicted prevalence of PES from the plot () and calculate the number of PES-positive subjects at the end of the study for each age group. For example, the eventual median age for the 65–69years old is 85years, prevalence of PES 28.5%, and number of PES-positive subjects 143 (as compared to 67years, 11.0% and 55 at baseline — an increase of 88 subjects). Repeating this across all age groups returns a total number of 575 rather than 319 PES-positive subjects. If those who converted to PES-positive had similar survival than those who were PES-positive at baseline, the median life length of the PES-negative subjects would have been somewhat higher, but not much; for example, the estimated median life span for those 65–69years old would be 4months longer. This bias is unlikely to change the main results. However, another source of bias that the authors acknowledge, namely analyzing only all-cause mortality, cannot be dismissed as potentially hiding clinically meaningful differences in cause-specific mortality. PES has only been suspected of increasing cardio- and cerebrovascular mortality (). It has not been implicated in cancer, another major cause of death. Moreover, PES has often been less common among diabetic patients (for references see ). Because cardiovascular complications of diabetes shorten survival, this diminishes chances of detecting any mortality excess from PES. Luckily, this bias can still be addressed by , because causes of death are generally obtainable for valid research purposes. There is, consequently, scope for Act 3 before excluding shortened life spans in a subset of PES-positive subjects.