Case-control sampling is a commonly used retrospective sampling design to alleviate imbalanced structure of binary data. When fitting the logistic regression model with case-control data, although the slope parameter of the model can be consistently estimated, the intercept parameter is not identifiable, and the marginal case proportion is not estimatable, either. We consider the situations in which besides the case-control data from the main study, called internal study, there also exists summary-level information from related external studies. An empirical likelihood based approach is proposed to make inference for the logistic model by incorporating the internal case-control data and external information. We show that the intercept parameter is identifiable with the help of external information, and then all the regression parameters as well as the marginal case proportion can be estimated consistently. The proposed method also accounts for the possible variability in external studies. The resultant estimators are shown to be asymptotically normally distributed. The asymptotic variance-covariance matrix can be consistently estimated by the case-control data. The optimal way to utilized external information is discussed. Simulation studies are conducted to verify the theoretical findings. A real data set is analyzed for illustration.

Development of comprehensive prediction models are often of great interest in many disciplines of science, but datasets with information on all desired features typically have small sample sizes. In this article, we describe a transfer learning approach for building high-dimensional generalized linear models using data from a main study that has detailed information on all predictors, and from one or more external studies that have ascertained a more limited set of predictors. We propose using the external dataset(s) to build reduced model(s) and then transfer the information on underlying parameters for the analysis of the main study through a set of calibration equations, while accounting for the study-specific effects of certain design variables. We then use a generalized method of moment (GMM) with penalization for parameter estimation and develop highly scalable algorithms for fitting models taking advantage of the popular glmnet package. We further show that the use of adaptive-Lasso penalty leads to the oracle property of underlying parameter estimates and thus leads to convenient post-selection inference procedures. We conduct extensive simulation studies to investigate both predictive performance and post-selection inference properties of the proposed method. Finally, we illustrate a timely application of the proposed method for the development of risk prediction models for five common diseases using the UK Biobank study, combining baseline information from all study participants (500K) and recently released high-throughout proteomic data (# protein = 1500) on a subset (50K) of the participants.