The DOI matches its Crossref record; 47 of the 47 references it cites were found in a registry or an index.
Guide to Bone Health and Disease in Cystic Fibrosis
Abstract
Cystic fibrosis (CF) is the most common genetic disease within the Caucasian population and leads to premature respiratory failure. Approximately 60,000 individuals are currently living with CF in North America and Europe, 40% of whom are adults. The life span of these patients has increased from approximately 2 to 32 yr of age over the last three decades. Bone disease has emerged as a common complication in long-term survivors of CF. Some studies have observed that 50-75% of adults have low bone density and increased rates of fractures. Prevention and treatment of CF-related bone disease must address the myriad risk factors (decreased absorption of fat-soluble vitamins due to pancreatic insufficiency, altered sex hormone production, chronic lung infection with increased levels of bone-active cytokines, physical inactivity, and glucocorticoid therapy) for poor bone health. This review is a condensed and updated summary of the Guide to Bone Health and Disease in Cystic Fibrosis: A Consensus Conference, a statement that evolved from a meeting convened by the Cystic Fibrosis Foundation in May 2002 to address the pathogenesis, diagnosis, and treatment of bone disease in CF. The goal of this conference was to develop practice guidelines for optimizing bone health in patients with CF.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Manolagas, S. C., & Jilka, R. L. (1995) · New England Journal of Medicine · doi:10.1056/nejm199502023320506 · Cited by 1,668
Bailey, D. A., Mckay, H. A., Mirwald, R. L., Crocker, P. R. E., & Faulkner, R. A. (1999) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.1999.14.10.1672 · Cited by 1,030
Consensus Report on Nutrition for Pediatric Patients With Cystic Fibrosis
Borowitz, D., Baker, R. D., & Stallings, V. (2002) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1002/j.1536-4801.2002.tb07816.x · Cited by 581
Self-citationEffects of Diabetes Mellitus on Bone Mass in Juvenile and Adult-Onset Diabetes
Levin, M. E., Boisseau, V. C., & Avioli, L. V. (1976) · New England Journal of Medicine · doi:10.1056/nejm197601292940502 · Cited by 519
Acquisition of optimal bone mass in childhood and adolescence
Bachrach, L. K. (2001) · Trends in Endocrinology & Metabolism · doi:10.1016/s1043-2760(00)00336-2 · Cited by 422
Self-citationAris, R. M., Renner, J. B., Winders, A. D., Buell, H. E., Riggs, D. B., Lester, G. E., & Ontjes, D. A. (1998) · Annals of Internal Medicine · doi:10.7326/0003-4819-128-3-199802010-00004 · Cited by 302
Self-citationSevere Osteoporosis Before and After Lung Transplantation
Aris, R. M., Neuringer, I. P., Weiner, M. A., Egan, T. M., & Ontjes, D. (1996) · Chest · doi:10.1378/chest.109.5.1176 · Cited by 267
Self-citationOsteoporosis after Organ Transplantation
Rodino, M. A., & Shane, E. (1998) · The American Journal of Medicine · doi:10.1016/s0002-9343(98)00081-3 · Cited by 249
Osteoporosis in lung transplantation candidates with end-stage pulmonary disease
Shane, E., Silverberg, S. J., Donovan, D., Papadopoulos, A., Staron, R. B., Addesso, V., Jorgesen, B., McGregor, C., & Schulman, L. (1996) · The American Journal of Medicine · doi:10.1016/s0002-9343(96)00155-6 · Cited by 243
Low bone mineral density in adults with cystic fibrosis
Haworth, C. S., Selby, P. L., Webb, A. K., Dodd, M. E., Musson, H., Niven, R. M., Economou, G., Horrocks, A. W., Freemont, A. J., Mawer, E. B., et al. (1999) · Thorax · doi:10.1136/thx.54.11.961 · Cited by 224
Self-citation
Cited by
Holick, M. F. (2007) · New England Journal of Medicine · doi:10.1056/nejmra070553 · Cited by 13,720
Self-citationO'Sullivan, B. P., & Freedman, S. D. (2009) · The Lancet · doi:10.1016/s0140-6736(09)60327-5 · Cited by 1,320
ECFS best practice guidelines: the 2018 revision
Castellani, C., Duff, A. J. A., Bell, S. C., Heijerman, H. G. M., Munck, A., Ratjen, F., Sermet-Gaudelus, I., Southern, K. W., Barben, J., Flume, P. A., et al. (2018) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2018.02.006 · Cited by 765
European cystic fibrosis society standards of care: best practice guidelines
Smyth, A. R., Bell, S. C., Bojcin, S., Bryon, M., Duff, A., Flume, P., Kashirskaya, N., Munck, A., Ratjen, F., Schwarzenberg, S. J., et al. (2014) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2014.03.010 · Cited by 582
Diagnosis and treatment of endocrine comorbidities in patients with cystic fibrosis
Siwamogsatham, O., Alvarez, J. A., & Tangpricha, V. (2014) · Current Opinion in Endocrinology, Diabetes & Obesity · doi:10.1097/med.0000000000000096 · Cited by 36
Metadata
- Authors
- Aris, R. M., Merkel, P. A., Bachrach, L. K., Borowitz, D. S., Boyle, M. P., Elkin, S. L., Guise, T. A., Hardin, D. S., Haworth, C. S., Holick, M. F., Joseph, P. M., O’Brien, K., Tullis, E., Watts, N. B., & White, T. B.
- Venue
- The Journal of Clinical Endocrinology & Metabolism
- Publisher
- The Endocrine Society
- Published
- 2005-03
- Volume
- 90
- Issue
- 3
- Pages
- 1888-1896
- ISSN
- 0021-972X (ISSN-L)
- 1945-7197
- OpenAlex
- W2146555387
- Cited by
- 451
- References
- 47
- FWCI
- 18.74
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Guide to Bone Health and Disease in Cystic Fibrosis. https://app.cochat.ai/papers/10.1210/jc.2004-1629
- The paper
- Aris, R. M., Merkel, P. A., Bachrach, L. K., Borowitz, D. S., Boyle, M. P., Elkin, S. L., Guise, T. A., Hardin, D. S., Haworth, C. S., Holick, M. F., Joseph, P. M., O’Brien, K., Tullis, E., Watts, N. B., & White, T. B. (2005). Guide to Bone Health and Disease in Cystic Fibrosis. The Journal of Clinical Endocrinology & Metabolism. https://doi.org/10.1210/jc.2004-1629
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.