- Season of Birth category listing has
23 items along with related searches
- Multiple Sclerosis 23 percent more likely if born in April vs. Oct – meta-analysis Nov 2012
- Environmental risk factors for MS include latitude and vitamin D – Sept 2012
- Hypothesis- birth rate variation with season may trump MS variation with vitamin D – Jan 2014
- Odds of living to 100 increase by 40 percent if had been born in the fall – 2011
- Season of birth associated with pneumonia (10 pcnt) and multiple sclerosis (30 pcnt) – May 2013
- Schizophrenia increased 40 percent for Spring births after Danes stopped vitamin D fortification – April 2014
- Is the variation in winter babies due to vitamin D – 2009
- Serotonin related to season, light and perhaps latitude and vitamin D
- Association between season of birth and suicide – perhaps vitamin D – Sept 2012
- Headaches vary with latitude and season and perhaps vitamin D as well -May 2010
- Season of birth (Vitamin D) vs birth weight, puberty, body size, etc. – Oct 2015
- UV at time of conception associated with Vitamin D Receptor activation 65 years later – Sept 2017
- Diseases correlated to month of birth – 2008 which has the following chart
Your Birth Month Influences Your Risk for Diseases Discover Mag review of the study
- "In all, researchers identified 16 diseases that were never before associated with birth month, and they also confirmed results from past studies. "
- . . . the study only examined data collected from one hospital in New York City; therefore, health data may be skewed due to New York’s climate.
- Furthermore, sick patients tend to be overrepresented in electronic health records, because, well, they are visiting the doctor more often.
J Am Med Inform Assoc 2015;0:1–15. doi:10.1093/jamia/ocv046, Research and Applications
Mary Regina Boland1,2, Zachary Shahn3, David Madigan2,3, George Hripcsak1,2 Nicholas P. la
* Correspondence to Nicholas Tatonetti, PhD, Department of Biomedical Informatics, Department of Systems Biology, Department of Medicine, Columbia University,
622 West 168th Street, VC-5, New York, NY 10032, USA; nick.tatonetti at columbia.edu
Objective An individual’s birth month has a significant impact on the diseases they develop during their lifetime. Previous studies reveal relationships between birth month and several diseases including atherothrombosis, asthma, attention deficit hyperactivity disorder, and myopia, leaving most diseases completely unexplored. This retrospective population study systematically explores the relationship between seasonal affects at birth and lifetime disease risk for 1688 conditions.
Methods We developed a hypothesis-free method that minimizes publication and disease selection biases by systematically investigating disease-birth month patterns across all conditions. Our dataset includes 1 749 400 individuals with records at New York-Presbyterian/Columbia University Medical Center born between 1900 and 2000 inclusive. We modeled associations between birth month and 1688 diseases using logistic regression. Significance was tested using a chi-squared test with multiplicity correction.
Results We found 55 diseases that were significantly dependent on birth month. Of these 19 were previously reported in the literature (P< .001), 20 were for conditions with close relationships to those reported, and 16 were previously unreported. We found distinct incidence patterns across disease categories.
Conclusions Lifetime disease risk is affected by birth month. Seasonally dependent early developmental mechanisms may play a role in increasing lifetime risk of disease.
Key words: Electronic health records; personalized medicine; seasons; cardiovascular diseases; embryonic and fetal development; prenatal nutritional physiological phenomena; pregnancy; maternal exposure.
Hippocrates described a connection between seasonality and disease nearly 2500 years ago, “for knowing the changes of the seasons ... how each of them takes place, he [the clinician] will be able to know beforehand what sort of a year is going to ensue ... for with the seasons the digestive organs of men undergo a change.”1 Following in footsteps laid more than 2 millennia ago, recent studies have linked birth month with neurological,2-4 reproductive,5-9 endocrine10 and immune/ inflammatory disorders,11 and overall lifespan.12
Many disease-dependent mechanisms exist relating disease-risk to birth month. For example, evidence linking a subtype of asthma to birth month was presented in 1983.13
EHR data requires overcoming problems with definition discrepancies,19 data sparseness, data quality,20 bias,21 healthcare process effects,22 and privacy issues.23 Informatics methods overcome these challenges, e.g., standardized ontologies minimize definition discrepancies,24 concordance measured across integrated datasets allows for data sparseness and quality assessment,20 and statistical methods can minimize bias and healthcare process effects.25-27 Using informatics approaches, EHR discovery methods28 were developed with successful applications in diverse areas including: dentistry,29 genetics,30-32 and pharmacovigilance.33,34 Novel disease association patterns35,36 and seasonal dependencies37-39 have also been established using EHRs.
Advances in health informatics coupled with the availability of large clinical databases enable systematic investigation of birth month-disease dependencies. All previous disease-birth month association studies were hypothesis-driven and focused on popular diseases leaving rare diseases unstudied (selection bias). Also, in the literature there is a propensity to publish studies that find an association over those that fail to find a relationship, illustrating publication bias.26,27,40,41 In contrast, we developed a high-throughput, hypothesis-free algorithm that mines for disease-birth month associations across millions of records. We call our approach: Season-Wide Association Study (SeaWAS) as it finds all conditions associated with birth month. We show that SeaWAS detects diseases with seasonal components related to early development.
We used the Columbia University Medical Center (CUMC)’s health record data, previously converted to the standardized Common Data Model (CDM) developed by the Observational Medical Outcomes Partnership (now the Observational Health Data Sciences and Informatics).42 CUMC data was initially recorded using International Classification of Diseases, version 9 (ICD-9) codes. These ICD-9 codes were mapped to Systemized Nomenclature for Medicine-Clinical Terms (SNOMED-CT) codes according to the CDM v.4.42 We selected SNOMED-CT because it captures more clinical content then ICD-9 codes,43 making SNOMED-CT ideal for phenotype classification. Additionally, using this standardized CDM increases the portability of our method across institutions enhancing data sharing.44
We extracted all individuals born between 1900 and 2000 inclusive (N = 1749400 individuals) who were treated at CUMC (between 1985 and 2013), demographics given in Table 1. The median age of our population was 38 years (interquartile range, IQR: 22-58). We performed a Fisher-exact test between the birth month distributions for each sex vs the average birth month distribution. Likewise the birth month distributions by birth decade (e.g., 1900-1909,1990-1999) were compared to the overall average birth month distribution. No statistically significant differences were found (P = 1 for all comparisons). Therefore, yearly and sex-based variation in the birth month distribution is minimal and should not affect our analyses (SI Appendix Figure S1 and S2).
We verified that our monthly birth rate data was consistent with known New York City (NYC) births using data from the Centers of Disease and Control (CDC) for 1990-2000 inclu- sive.45 CUMC data were highly correlated with CDC birth rates from the Bronx (r = 0.833, P = .001), New York (r = 0.796, P = .002), and Queens (r = 0.791, P = .002) counties (SI Appendix Figure S3). We performed this verification check because confirming the place of birth for individuals can be complex,46 and was not possible for our CUMC dataset. Subsequently, for the 1990-2000 period we were able to obtain data regarding the number of babies admitted to CUMC on the day of their birth for the 1990-2000 period and found that the proportion (no. of patients admitted to CUMC on their day of birth/no. of patients included in SeaWAS) ranged from 17.97% to 31.28% by birth year with the average proportion being 22.98%. CUMC’s Institutional Review Board approved this study.
We investigated associations with birth month across all recorded conditions. A condition is defined as any SNOMED-CT code mapped using the CDM.42 For controls, we randomly sampled individuals from the same EHR population without the disease ensuring that our control sample size was ten times the size of the case population. We then modeled the association between birth month (as an integer) and each condition as a logistic regression model with significance assessed using chi-square (R v.3.1.0). Therefore, the monthly birth rate was compared between the case and control populations for each condition adjusting for monthly birth month variation effects. For multiplicity correction, we only selected conditions passing the Benjamini-Hochberg adjustment that controls for the false discovery rate (FDR).47 To ensure sufficient sample size across all 12 months, we only investigated conditions having at least 1000 individuals born between 1900 and 2000 inclusive (this amounted to 1688 conditions).
To evaluate SeaWAS, we extracted all articles from PubMed with the term “birth month” and an additional article referenced by a located article (n = 156). We manually reviewed all abstracts and removed articles related to nonhumans (n = 8), breeding (n = 7), sports (n = 10), or where birth month was used for another purpose, e.g., for matching controls (n = 34), perspective/meta-analysis papers (n = 2), papers not available in English (n = 2), and one paper with a statistical error noted in PubMed. This process identified 92 relevant articles. We then manually classified each paper by the disease studied, and whether they found or failed to find an association. Some conditions associated with birth month in the literature, e.g., height, were not extractable from our EHR (36 diseases were not extractable). In total, 19 diseases reported in the literature could be mapped to EHR conditions. Of those diseases, 16 were positively associated (>50% of literature supported an association) and 3 were not associated (<50% of literature failed to find an association). We extracted all relevant EHR codes for each of the 16 positive associations (n = 172 codes).
Table 1: Demographics of Patients Included in SeaWAS Study (N = 1749400)
These literature associations were used for quality assessment of SeaWAS results.
We used an internal evaluation technique to evaluate novel associations discovered by SeaWAS. We ran the SeaWAS algorithm on a restricted sample comprising 80% of the original sample, randomly chosen. We then corrected for multiplicity using the Benjamini-Hochberg adjustment that controls the FDR. We took all novel associations (i.e., not reported in the literature) revealed in the restricted sample, and then validated them using the validation set (containing 20% of the original population). Twelve of the 16 discovered associations were validated in this manner.
Permutation analysis was also used for empirical evaluation of SeaWAS. We randomly selected 55 diagnosis codes from the set of 1688 codes included in our study. We then set all codes in this randomly derived set as “positive” associations. Next, the number of positive literature results in each random sample was measured. This was done for 1000 random samples. The overall distribution of these random samples was compared to our SeaWAS results. This allowed us to assess the true positive rate, false positive rate, positive predictive value, and the total number of confirmed literature associations obtained from SeaWAS.
For all significant associations, we calculated the proportion of individuals having the condition using their birth month and day out of all individuals with the same birth month and day. This generated a set of proportions for every day in the year (366 days). We then used a 2-month window10 to smooth the daily proportion rate (1 month before the date and 1 month after the date). The weekly and monthly averages were then computed. An overview of the algorithm is shown in Figure 1.
All SeaWAS results were compared to the literature in a binary manner to ascertain if the association was previously reported. Afterwards, we analyzed the disease-birth month risk plots from the literature. We used three criteria to select studies, namely: 1) published raw data; 2) raw data includes some adjustment for natural variation in birth month depending on study region; and 3) disease-birth month data were at a similar granularity level to allow for effective comparisons (e.g., this criterion would exclude studies that grouped multiple diseases together or removed certain disease subtypes). We sought to include pattern data for at least one study per disease category to compare with SeaWAS.
EHR Mining of 1688 Conditions Reveals 55 Conditions Dependent on Birth Month
We used SeaWAS to mine birth month associations for 1688 SNOMED-CT conditions with at least 1000 individuals recorded at CUMC. After multiplicity correction using FDR (a = 0.05, n = 1688 conditions), 55 conditions were found associated with birth month. All reported P-values are FDR adjusted (q-values).
Literature Validation of SeaWAS Results Using our curated reference set of 16 conditions (that mapped to 172 SNOMED-CT codes), we found 19 SeaWAS results (7 distinct diseases) were supported by the literature (SI Appendix Table S1), representing a significant enrichment with OR = 3.4 (95% CI: 1.9-6.0, P< .0001, Figure 2a). SeaWAS successfully ruled-out associations between birth month and disease risk for all “true negatives” in our reference set (Figure 2a). We compared SeaWAS results for known and closely related diseases (Figure 2b) to help elucidate gaps in the literature. We found that some diseases, e.g., reproductive performance, featured prominently in both the literature and SeaWAS results, whereas, other diseases featured heavily in the literature but not as strongly in our results, e.g., asthma/allergy and rhinitis. A potential literature gap exists for respiratory syncytial virus (2 publications Figure 2a), which had many SeaWAS known or highly related associations (8 total Figorithm takes all 1688 conditions as initial input, finds significant associations over all months, then it models each birth month’s association with the condition by smoothing the birth month proportions using associations, Figure 2b). A Manhattan plot visualizes our results by disease category (Figure 2c) showing that some categories including, circulatory, and respiratory diseases appear prominently in our results.
We found 20 conditions associated with birth month that were similar to those in our reference set (SI Appendix Table S2) and 16 that were completely novel (Table 2). Nine of these 16 associations were cardiovascular conditions including: atrial fibrillation (P< .001), essential hypertension (P< .001), congestive cardiac failure (P< .001), angina (P = .001), cardiac complications of care (P= .027), mitral valve disorder (P = .024), pre-infarction syndrome (P = .036), cardiomyopathy (P = .009), and chronic myocardial ischemia (P = .022). Seven discovered associations were non-cardiovascular: primary malignant neoplasm of prostate, malignant neoplasm of overlapping lesion of bronchus and lung, acute upper respiratory infection, nonvenomous insect bite, venereal disease screening, bruising, and vomiting.
Internal Evaluation of Discovered Associations We internally evaluated all novel associations found using SeaWAS. We ran SeaWAS on an 80% restricted sample and then validated the novel associations in the validation set (20% original sample size). 12 of the 16 novel associations were validated including 6 out of 9 novel cardiovascular conditions. Table 2 denotes the discovered conditions that passed the internal validation. Four conditions were not significant after correction in the restricted sample including: mitral valve disorder, pre-infarction syndrome, chronic myocardial ischemia, and vomiting.
Evaluation Using Permutation Analysis We used permutation analysis to assess the concordance we found between our SeaWAS results and what was reported in the literature. We randomly selected 55 codes from the set of 1688 codes included in our study and set them as “positives.” We then measured the number of positive literature results in our random samples and compared to SeaWAS. We did this for 1000 random samples. Results are shown in Figure 3. SeaWAS consistently and significantly (P< .001) outperformed random for TPR, FPR, and PPV at finding more literature validated associations.
Asthma, Reproductive Performance, and ADHD We calculated smoothed birth month proportions for all 55 SeaWAS birth month associations. We then compared conditions with known associations to birth month and their published trends. The smoothed weekly and monthly proportions are shown in Figure 4 for 3 established associations: asthma, Attention Deficit Hyperactivity Disorder (ADHD) and reproductive performance and three discovered associations: atrial fibrillation, mitral valve disorder, and chronic myocardial ischemia. Relative risk plots for the associations are given in SI Appendix Figure S4. To compare our results with the published proportions from other studies, we used an asthma study from Denmark,13 a reproductive performance study from Austria,8 and an ADHD study from Sweden.3
Comparing our results with Denmark’s asthma study13 showed highly similar seasonal patterns. They found two large peaks in May and August, with 2 smaller peaks in June and July.13 Our results were shifted by 2 months with large peaks in July and October and smaller peaks in August and September. We extracted data on the average monthly sunshine exposure for NYC and Denmark48,49 for comparison (Figure 4). For reproductive performance, we compared our results to an Austrian study8 (Figure 4). We validated a dip in births among females born in May through September as this was also found in the Austrian study. We compared our ADHD smoothed proportions to odds ratios reported by a Swedish study and found a similar upward trend towards the later part of the year peaking in November3 (Figure 4).
Many diseases demonstrate birth month dependencies with known mechanistic etiologies, including: asthma,13 ADHD,3 reproductive performance,8 and myopia.50 In these studies birth month was used as a proxy for seasonal variations in physiological state or changes in environmental exposures. Understanding dependencies between diseases and these variations is an important and challenging research task. Large clinical databases, such as EHRs, represent a novel resource for systematically investigating diseases.17,18 We present a novel method, SeaWAS, for investigating birth-month dependencies across all diseases in a large EHR. Prior studies analyzed a single disease, or a disease spectrum (e.g., Immune-mediated Diseases) at a time. These hypothesis- driven methods suffer from publication bias, whereby papers demonstrating an association between a disease of interest and birth month are more likely to be published than papers that fail to find an association.26,27,40 Prior methods also suffer from disease selection bias whereby diseases of popular interest are studied more frequently potentially overlooking other important disease-birth month associations. SeaWAS overcomes these challenges using a hypothesis-free method that does not relying on a priori hypotheses.
SeaWAS Confirms Known Disease-Birth Month Associations SeaWAS confirmed a literature-validated association between asthma (hyper-reactive airway disease) and birth month reported by studies from Denmark13 and Sweden.51 When we compared our findings to the Denmark study,13 we found a 2- month shift in the birth month-asthma pattern that corresponds with a shift in the peak sunshine (a factor in asthma complicated by dust mite allergies) between Denmark and NYC48,49 (Figure 4).
Likewise, comparing our reproductive performance results to an Austrian study8 revealed that the dip in births among females born in May through September was observed in both studies.8 Importantly, the female reproductive system, unlike males, is established early with females being born with their lifetime maximum number of oocytes.52,53 Oocyte count is thought to be linked to fertility.54 Many studies show a link between maternal birth month and number of offspring supporting the belief that prenatal and early developmental effects can alter a female’s lifetime fertility.5-9 SeaWAS findings bolster this body of literature.
We compared our ADHD smoothed proportions to odds ratios reported by a Swedish study and found a similar upward trend towards the later part of the year peaking in November.3
A rationale for their findings (and ours) is that relative immaturity (born later in the year) may result in increased ADHD detection.3 This occurs because more immature children (i.e., younger in age) face higher demands early on in their school years making them more susceptible to ADHD diagnosis. The age cutoff for schools in Sweden is 31 December, which is the same for NYC public schools. Alternatively, the relationship between Vitamin D and ADHD and learning patterns has been established in rats55,56 and Vitamin D deficiency in early development (in utero or shortly after birth) could be related to ADHD.
Discovered Cardiac Condition-Birth Month Relationship SeaWAS revealed nine cardiovascular conditions associated with birth month. Importantly, children born to survivors of the H1N1 1918 subtype were associated with a >20% excess risk of cardiovascular disease,57 suggesting a relationship between maternal infection and cardiovascular disease risk that is independent of maternal malnutrition.57 Therefore, maternal infection during the winter months (January-March) could contribute to the increased cardiovascular disease risk among children born in those months.
Looking at all 10 (9 novel) cardiovascular conditions revealed that individuals born in the autumn (September- December) were protected against cardiovascular conditions while those born in the winter (January-March) and spring (April-June) were associated with increased cardiovascular disease risk (Figure 5). Interestingly, one study found that people born in the autumn (October-December) lived longer than those born in the spring (April-June).12 Furthermore the relationship between cardiovascular disease risk and lifespan is established.58 We compared our results to the Doblhammer et al. study investigating lifespan’s dependency on birth month and found 6 cardiovascular diseases were significantly anticorrelated. This indicates that birth months with low risk for 6 cardiovascular diseases in our study were also associated with longer lifespan in Doblhammer’s study12 (Figure 6). Our findings suggest that the relationship between lifespan and birth month12 could be explained by increased cardiovascular disease risk.
The relationship between cardiovascular disease and birth month could be mediated through a developmental Vitamin D-related pathway. Serum 25-hydroxyvitamin D levels are lower and parathyroid hormone levels are higher during the winter when no supplementation is given.59 Even with maternal supplementation, seasonally dependent Vitamin D deficiency has been observed among breastfed infants60 and newborns.61 This is important because levels of parathyroid hormone and Vitamin D are associated with cardiovascular disease.62,63 Specifically, elevated parathyroid hormone is correlated with increased heart failure in elderly males.64 Studies focusing on adolescents found that Vitamin D deficiency resulted in an increased likelihood of hypertension (a SeaWAS discovered as- sociation)65,66 and high-density lipoprotein cholesterol,66 both risk factors for cardiovascular disease.
SeaWAS vs PheWAS: Looking Towards the Future We present SeaWAS a Phenome-Wide approach that systematically investigates birth month-disease dependencies using EHRs. Our method uses birth month as a proxy for prenatal or perinatal exposure/effects of seasonality on development, and the disease-risk conferred by these perturbations. Denny et al.’s30 Phenome-Wide Association Study (PheWAS) investigates the relationship between diseases recorded in EHRs and genomic markers in a similar high-throughput manner. Recently, an obesity risk factor gene was found to be associated with year of birth67 suggesting the importance of combined genetic-environmental etiologies in complex phenotypes. In the near future it may be possible to harness SeaWAS and PheWAS methods for high-throughput identification of diseases tied to prenatal environmental factors (SeaWAS) and then reveal the genetic drivers (PheWAS) underlying the prenatal seasonality effects from EHRs.
Study limitations include the lack of condition independence (conditions rarely occur in isolation) potentially affecting multiplicity correction. Also, we cannot rule out indirect mechanisms (e.g., depression affects fertility, and learning ability) behind associations between disease risk and birth month. Some conditions associated with birth month may be associated because the infant was born in a high-risk period, e.g., acute bronchiolitis-autumn births. These associations differ from lifetime disease effects; however, we do not distinguish between them in our analyses because both are presented in the literature as birth month-disease associations. Another limitation is our exclusive use of EHR data, which is affected by the healthcare process22,68 and can introduce bias,21 e.g., sick patients tend to be over-represented in EHR populations.69 Importantly, we showed that our birth month by year data correlated with CDC data (SI Appendix Figure S3) indicating that our EHR population adequately represents the “true” NYC-born population (which includes healthy people) with respect to birth month. Hence, we do not expect this bias to affect our findings.
Additionally, our study uses one institution’s data only; therefore, all birth month-disease risk findings are based on the NYC climate. Because our data is from one locale and climate, the effects we observe are likely due to the climate effects of the NYC region, and is most comparable to Northern European climates. Future work, involves applying our SeaWAS methodology to other institutions and adjusting for climatic differences, which is important when including data from diverse locales and climates.70
We present a high-throughput algorithm called SeaWAS that uncovers conditions associated with birth month without relying on a priori hypotheses. SeaWAS confirms many known connections between birth month and disease including: reproductive performance, ADHD, asthma, colitis, eye conditions, otitis media (ear infection), and respiratory syncytial virus. We discovered 16 associations with birth month that have never been explicitly studied previously. Nine of these associations were related to cardiovascular conditions strengthening the link between cardiac conditions, early development, and Vitamin D. Seasonally-dependent early developmental mechanisms might play a role in increasing lifetime disease risk.
M. R.B.: Ms. Boland designed methodology, conducted all analyses, and wrote the manuscript.
Z.S.: Mr Shahn helped with statistical analyses, reviewed, and noted points of revision for the manuscript.
D.M.: Dr Madigan engaged in the design of the statistical methods, reviewed, and noted points of revision for the manuscript.
G.H.: Dr Hripcsak helped design aspects of the methodology particularly as they pertained to appropriate use of Electronic Health Records, provided guidance on the interpretation of the analyses, and reviewed the manuscript.
N. P.T.: Dr Tatonetti was involved in all stages of the study design and implementation. He contributed resources, helped refine aspects of the methodology, provided critical insights into validation of methods, and critically reviewed and edited the manuscript.
The authors have no financial disclosures relevant to this article.
CONFLICT OF INTEREST
The authors have no conflicts of interest.
CLINICAL TRIAL REGISTRATION
Supplementary material is available online at http://jamia. oxfordjournals.org/.
M.R.B. was supported by the National Library of Medicine training grant T15 LM00707, G.H. supported by LM006910, N.P.T. supported by R01 GM107145.
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