Hypothyroidism is often diagnosed, and subsequently treated, due to health-related quality of life (HRQL) issues. However, HRQL following treatment has never previously been assessed in longitudinal descriptive studies using validated instruments.
To investigate disease-specific (ThyPRO) and generic (SF-36) HRQL, following levothyroxine therapy in patients with hypothyroidism due to autoimmune thyroiditis.
This prospective cohort study was set at endocrine outpatient clinics at two Danish university hospitals. Seventy-eight consecutive patients were enrolled and completed HRQL questionnaires before, six weeks, and six months after initiation of levothyroxine therapy. Normative ThyPRO (n = 739) and SF-36 (n = 6,638) data were available for comparison and changes in HRQL following treatment were estimated and quantified.
Prior to treatment, all ThyPRO scales were significantly impacted (p<0.0001), compared to the general population sample. The same was observed for seven of eight SF-36 scales, the exception being Bodily Pain. Tiredness (ThyPRO) and Vitality (SF-36) were the most markedly impacted scales. After six weeks of treatment, nine of thirteen ThyPRO scales had significantly improved. ThyPRO improvements were consistent at six months, where five of eight SF-36 scales had also significantly improved, but deficits persisted for a subset of both ThyPRO and SF-36 scales.
In this population of hypothyroid patients, HRQL was widely affected before treatment, with tiredness as the cardinal impairment according to both ThyPRO and SF-36. Many aspects of HRQL improved during the first six months of LT4 therapy, but full recovery was not obtained. Our results may help clinicians inform patients about expected clinical treatment effects.
Citation: Winther KH, Cramon P, Watt T, Bjorner JB, Ekholm O, Feldt-Rasmussen U, et al. (2016) Disease-Specific as Well as Generic Quality of Life Is Widely Impacted in Autoimmune Hypothyroidism and Improves during the First Six Months of Levothyroxine Therapy. PLoS ONE 11(6): e0156925. https://doi.org/10.1371/journal.pone.0156925
Editor: Karen M. Tordjman, Tel Aviv Sourasky Medical Center, ISRAEL
Received: March 6, 2016; Accepted: May 20, 2016; Published: June 3, 2016
Copyright: © 2016 Winther et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: Our data are deposited publicly at the Danish Data Archive. Citation: Torquil Watt, Validation and internationalization of the thyroid-specific quality of life questionnaire ThyPRO and its application in a randomized controlled clinical trial, 2008–2013, Dansk Data Arkiv, 2014. 1 data file: DDA-23924, version: 1.0.0, http://dx.doi.org/10.5279/DK-SA-DDA-23924.
Funding: This study was supported by research grants from the Danish Agency for Science, Technology and Innovation: Council for Strategic Research and Council for Independent Research (ID: 09-066886), and Agnes & Knut Mørks Foundation. KHW is supported by grants from the University of Southern Denmark and the Region of Southern Denmark; UFR and LH are supported by an unrestricted grant from the Novo Nordisk Foundation. SB is supported by grants from Odense University Hospital Research Council. JBB is an employee of Optum Patient Insights. The above funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of all authors are articulated in the ‘author contributions’ section.
Competing interests: JBB is commercially affiliated via his employment at Optum Patient Insights. This does not alter the authors' adherence to PLOS ONE policies on sharing data and materials.
Chronic autoimmune or Hashimoto’s thyroiditis (AIT) is common, and accounts for 85% of all cases of overt hypothyroidism in Denmark, where the overall annual incidence is approximately 47.2/100,000 [1,2]. The standard treatment is life-long levothyroxine (LT4) therapy, adjusting the dosage to achieve normal circulating thyrotropin (TSH) levels . However, recent investigations suggest that LT4 cannot ensure a euthyroid state in all tissues simultaneously , and cross-sectional studies have reported impaired psychological well-being and cognitive functioning in euthyroid AIT patients on LT4 [4–7]. Health-related quality of life (HRQL), measured by reported outcomes (PROs), is increasingly used when evaluating treatment effects in clinical studies and practice . Instruments can be divided into disease-specific and generic questionnaires. Combining the two types of measurement maximizes precision and sensitivity, and allows for comparability and interpretation across different patient groups and populations [9,10]. Measurement properties have been well-described for the most widely used generic instrument, SF-36 [11,12], while some currently available disease-specific instruments (4,6) have undergone initial validation in hypothyroid patients [6,13,14]. To further improve the measurement of HRQL in thyroid diseases, our group developed and validated the disease-specific ThyPRO questionnaire [15–20]. In AIT, HRQL has never previously been measured in descriptive longitudinal studies, and ThyPRO was chosen for this purpose since it is the only HRQL instrument that has been validated for responsiveness to treatment .
The objective of this prospective cohort study was therefore to investigate disease-specific (ThyPRO) and generic (SF-36) HRQL in patients with AIT before, during, and after six months of medical therapy with LT4, comparing their HRQL with that found in representative general population samples.
Materials and Methods
Design, setting and participants
This study was a prospective cohort study carried out from October 2008 to May 2012. Patients referred for hypothyroidism were consecutively recruited from the endocrine outpatient clinics at Copenhagen University Hospital, Rigshospitalet, and Odense University Hospital. The inclusion criteria were ≥18 years of age; indication for LT4 therapy treatment (patients had to be untreated at inclusion); positive thyroid peroxidase (TPO-Ab) and/or thyroglobulin (Tg-Ab) antibody concentrations according to local clinical guidelines; TSH concentrations >4.0 mIU/L; ability to complete paper-and-pencil questionnaires in Danish. Exclusion criteria were pregnancy and/or breastfeeding; thyroid cancer; previous radioiodine treatment or thyroid surgery; major comorbidities rendering completion of the study or interpretation of results improbable.
All patients were treated and followed according to local clinical guidelines, with regular blood sampling and visits in the outpatient clinics. After initiation of LT4 therapy, the dosage was adjusted aiming for TSH levels within the reference ranges. At Odense University Hospital, a booklet containing two questionnaires (ThyPRO and SF-36 v2) and additional questions on sociodemographics, comorbidity, and non-thyroid medication was handed out at the first visit. At Rigshospitalet, the same booklet was sent to eligible patients; after two weeks a reminder was sent to non-responders. Patients completed the ThyPRO questionnaire prior to and six weeks and six months after initiation of treatment with LT4, and the SF-36 v2 questionnaire prior to and six months after commencement of therapy. ThyPRO data after six weeks of LT4 therapy was originally collected for methodological purposes in connection with the validation of the ThyPRO instrument , but provided extra data in this clinical study. For the same reason SF-36 was not collected in this cohort at six weeks. The questionnaires were collected by mail. Clinical data on diagnosis, treatment and biochemical variables were obtained by medical chart review. Biochemical variables included serum TSH (reference range: 0.3–4.0 mIU/L), total serum thyroxine (T4) (65–135 nmol/L), serum TPO-Ab (<30 mIU/L) and serum Tg-Ab (<20 mIU/L). Subclinical hypothyroidism was defined as TSH concentrations above the reference range with T4 within the reference range, and overt hypothyroidism as TSH above the reference range and T4 below the reference range.
A subset of the data has previously been used for a methodological evaluation of the responsiveness of the ThyPRO questionnaire .
ThyPRO consists of 85 items on physical, mental and social domains of functioning and well-being in hypothyroidism, hyperthyroidism, non-toxic goiter, and Graves’ orbitopathy. The items employ a recall period of four weeks and are summarized in 13 multi-item scales and one single-item scale concerning Overall Impact of thyroid disease on HRQL. Each scale ranges 0–100, with higher scores indicating poorer health status. For specific items, please see the entire ThyPRO questionnaire (S1 Appendix).
The SF-36 consists of 36 items, also using a four week recall period, summarized in 8 scales. The scale scores can be further aggregated into physical and mental component summary scores. SF-36 scores were standardized using norm-based scoring to facilitate the comparison between SF-36 v1 (used in the general population sample) and v2 (used in the patient population). With norm-based scoring, mean and standard deviation (SD) is standardized to 50 and 10, respectively, in the general US population and higher scores indicate better health status.
General population samples
ThyPRO data from the Danish general population were gathered from a random sample of adult citizens, using the Danish Civil Registration System, as previously described . The questionnaire included items from the nine scales of the ThyPRO survey, which do not attribute HRQL-impact specifically to thyroid disease (in contrast to scales on impact of thyroid disease [Impaired Social Life, Daily Life, Sexlife, and Cosmetic Complaints]). The general population questionnaire also addressed socio-demographic variables, comorbidity, and medication. SF-36 data from the Danish general population were derived from the Danish Health Interview Survey in 2005, as described elsewhere [23,24]. For the present study we included general population data only for respondents living in the three regions from which patients were recruited.
To address a potential selection bias, the available socio-demographic baseline characteristics of non-responders and responders were compared using the Wilcoxon-Mann-Whitney (age) and Chi-square (gender, education, chronic disease). Changes in mean HRQL scale scores and biochemical measurements between baseline and six weeks and six months after initiation of LT4 therapy were analyzed with the paired Student’s t-test. Multiple linear regression analyses, adjusted for age, gender, comorbidity and educational status were performed to test for differences in HRQL scale scores between patients and the general population samples, for associations between HRQL scale scores and TSH, T4 and TPO-Ab concentrations, respectively, and to compare baseline HRQL scale scores between participants completing follow-up surveys, and those lost to follow-up. Biochemical measurements within the four week recall period were used for analyses. The magnitude of differences between the general population and patient samples was evaluated by effect sizes, calculated as the mean difference divided by the pooled SD of the general population sample and the patients at baseline. The magnitude of changes in patient scores following treatment was evaluated by effect sizes calculated as the mean change divided by the SD in the patient sample at baseline. In accordance with Cohen, an effect size of 0.2–0.5 was defined as small, 0.5–0.8 as moderate and >0.8 as large . P-values <0.05, were considered significant. All analyses were performed using SAS 9.4.
According to Danish law, questionnaire studies do not require and thus cannot obtain approval by ethical committees. A completed, returned questionnaire is regarded as consent. The study was approved by the Danish Data Protection Agency (#2007-58-0015) and conducted in accordance with the Declarations of Helsinki.
During 43 months, consecutive patients were screened and 100 patients with AIT were invited to participate. Seventy-eight patients completed the baseline (pre-treatment) survey (response rate 78%). In all, 63 patients completed follow-up surveys at six months, yielding a follow-up response rate of 81% of initially responding patients. The SF-36 was included in the surveys only after December 2009 and thus, 68 patients completed the SF-36 survey at baseline, and 58 (85% of initially responding patients) at six months. The median baseline age was 47 years, and 90% were females. All patients were treated with LT4 during the six-month study period. Socio-demographic characteristics, educational status, and comorbidity are shown in Table 1. There were no significant differences in baseline socio-demographic characteristics, biochemical measurements, or HRQL between the fifteen patients who completed only the baseline questionnaire and those completing the entire survey.
At baseline, the median (interquartile range) TSH was 8.1 (5.5–12.2) mIU/L, T4 was 82 (72–99) nmol/L, and TPO-Ab was 526 (221–1590) mIU/L. One participant had negative TPO-Ab but positive Tg-Ab concentration at 68 mIU/L. At baseline, 66 patients had subclinical and 12 patients had overt hypothyroidism. After six weeks of LT4 therapy, serum TSH significantly decreased (P<0.0001) to a median (interquartile range) of 3.0 (1.7–4.4) mIU/L, further decreasing to 2.6 (1.4–4.2) mIU/L at six months. T4 significantly increased (P<0.0001), as compared with baseline, with median (interquartile range) concentrations of 104 (92–117) nmol/L and 102 (80–118) nmol/L after six weeks and six months, respectively. After six months, 24 patients still had elevated serum TSH, 21 of whom had subclinical hypothyroidism.
Radar plot showing ThyPRO scale scores for patients with autoimmune hypothyroidism (AIT) at baseline and 6-months follow-up as well as scores from the general population sample. Each scale ranges 0–100, with higher scores indicating poorer quality of life. Items in ThyPRO scales marked* are asked with attribution to thyroid disease and cannot be answered by respondents from the general population.
Radar plot showing SF-36 scale scores for patients with autoimmune hypothyroidism (AIT) at baseline and 6-months follow-up as well as scores from the general reference population. Higher scores indicate better health status.
Comparison with general population samples before treatment.
Baseline ThyPRO scores among patients were significantly higher (worse) than the general population scores in all nine comparable scales (p-values <0.0001). Differences varied, from small effect sizes for Eye Symptoms and Anxiety to large effect sizes for Goiter Symptoms, Tiredness, and Emotional Susceptibility. The most severely impaired scale was the Tiredness scale (effect size: 1.05). Patients’ baseline SF-36 scores were lower (worse) than those in the general population sample in seven of eight scales, with effect sizes ranging from small to large, except for the Bodily Pain scale, where there was no difference. Large differences were seen in the Mental Health and Vitality scales, and the Mental Component summary score, with the largest difference for Vitality (effect size 1.37). There was no difference between patients and the general population sample in the SF-36 Physical Component summary.
Changes following medical therapy.
Scores significantly decreased (improved) for nine of thirteen ThyPRO scales as well as for overall HRQL after six weeks of therapy. All improvements, except Impaired Sexlife, were consistent after six months of therapy with additional significant improvements observed for the Depressivity and Cosmetic Complaints scales. All significant changes in the ThyPRO multi-item scales were of small magnitude, while the overall HRQL item improved with a moderate effect size, after six months of therapy (p<0.0001).
Six months after initiation of LT4 therapy, the SF-36 scales for Role-Physical, Bodily Pain, Vitality, Social Functioning and Mental Health, and the Mental Component summary score, had improved significantly, all with small effect sizes.
Comparison with general population samples at follow-up.
According to ThyPRO, there were no longer any large differences after six weeks of treatment, as compared with the general population samples. However, significant moderate differences persisted in physical Hypothyroid Symptoms and Tiredness, as did small differences in Goiter Symptoms and Cognitive Complaints. After six months, the same four scales remained significantly different from the general population sample. Only the Hypothyroid Symptoms scale attained a moderate effect size at this time point, while the other deficits were of small magnitude.
After six months of LT4 therapy several of the SF-36 scales, i.e. Mental Health, Role-Emotional, Social Functioning, Vitality, and the Mental Component, were still significantly impaired compared to the general population, showing moderate to small effect sizes.
Associations between biochemical measurements and HRQL
There were no significant associations between serum levels of TSH, total T4 or TPO-Ab and any of the ThyPRO or SF-36 scores, neither at baseline nor during follow-up. Neither were there any differences in the scores or effect of treatment, when comparing patients with subclinical (n = 66) versus overt hypothyroidism (n = 12) at baseline or follow-up.
In this prospective cohort study, we have assessed HRQL in patients with AIT. For the first time HRQL has been measured longitudinally in hypothyroid patients with both validated disease-specific (ThyPRO) and generic (SF-36) surveys, and compared with HRQL data from general population samples. Prior to LT4 therapy, we found significant impacts of varying magnitude across disease-specific (ThyPRO) and generic (SF-36) HRQL aspects, as compared to general population samples. Impairments ranged from large differences for Tiredness to small differences for Physical Functioning, while Bodily Pain was the only unaffected scale. The wide array of impacts was corroborated in a recent population-based case-control study of newly diagnosed overt AIT, with tiredness being the most frequently reported symptom . Since volunteer control subjects also experienced many symptoms indicative of hypothyroidism, the authors found that neither presence nor absence of individual symptoms is reliable for diagnosis of the disease . In addition, there were no associations between symptom burden and biochemical markers at disease onset . Thus, tiredness may be reported irrespective of disease or biochemical disease severity. Nevertheless, our study quantifies that tiredness is severely impacted in newly diagnosed AIT patients, as compared with the general population. After six weeks of treatment, we found a partial remission of the disease-specific tiredness, which further ameliorated at six months. However, a small to moderate impairment persisted, also when measured by the SF-36 Vitality scale. Thus, rather than reporting tiredness as a present/absent symptom, as is the classical diagnostic medical approach, quantifying it on a continuum, as done with ThyPRO, offers a more detailed picture of the course of disease symptomatology.
Deficits persisted for a subset of other disease-specific and generic scales. The ThyPRO scale showing the largest deficit at six months was the physical Hypothyroid Symptoms scale, including items such as “Have you been sensitive to cold?” and “Have you had dry skin?” This scale, along with Cognitive Complaints, did not respond to treatment during the study period. However, it has been suggested that persisting cognitive complaints, even in patients with subclinical hypothyroidism (the majority of our participants), are most likely an independent entity requiring separate evaluation . Another aspect of particular interest is the poorly understood relationship between hypothyroidism and depression . In a recent study both depressive symptoms and sexual dysfunction were related to subclinical hypothyroidism in female patients with AIT . We found depressivity moderately impacted in the untreated state, but this item improved during follow-up and was not significantly different, as compared with the general population, at the end of the study. The severity of sexual dysfunction cannot be compared with the general population in our study, as items in the ThyPRO scale for sexual impairments are asked with attribution to thyroid disease, and therefore irrelevant to the general population.
Many disease-specific issues significantly improved already within six weeks, with further improvements after six months, when the majority of SF-36 scales were also improved. All significant improvements were of small magnitude, except the ThyPRO overall HRQL item that improved with a moderate effect size at six months. This item asks the question: “During the past four weeks, has your thyroid disease had a negative effect on your quality of life?” It could be speculated that small improvements in various aspects accumulate, and lead to a larger overall effect.
Interestingly, we found similar impact and treatment effects when comparing patients with subclinical and overt hypothyroidism, supporting that also patients with mild biochemical thyroid failure benefit from treatment, at least from a HRQL point of view. This study was implemented in the daily-life clinic, reflected by the fact that approximately 30% of the patients had a TSH level above the reference range after six months of therapy. This is well in line with the Colorado thyroid disease prevalence study, where 40% of patients taking thyroid medication had abnormal TSH levels . Thus, suboptimal LT4 dose or poor patient compliance seems to be the rule and not unique to our study. It could be speculated that obtaining euthyroidism might have resulted in more pronounced HRQL improvements. However, we found no associations between thyroid function and HRQL in our regression analyses, and previous observations also suggest that normalization of TSH with LT4 does not safeguard against persistent complaints . Here, biochemical data, used for the regression analyses, were obtained by medical chart review. Future long-term studies should prospectively standardize the timing between measurement of HRQL and serum markers of thyroid function, in order to further elaborate the relationship between biochemical dysfunction and HRQL.
Strengths of our study are its longitudinal design, the use of validated disease-specific and generic questionnaires, and inclusion of general population reference groups. This conceptual framework can readily be applied to the study of quality of life in other diseases. However, there are also limitations. Although individuals lost to follow-up had similar sociodemographic characteristics they tended to have more impaired HRQL, albeit not statistically significant, as compared with patients who had a full survey. Three of fifteen patients (20%) lost to follow-up had overt hypothyroidism at baseline, while this number was 9/63 (14%) in patients with a full survey (9/63). This, as well as recruitment solely from university hospital outpatient clinics, may have induced selection bias. Generally, there was consistency between significance tests and effect sizes, but a minority of small differences or changes did not reach statistical significance, which may be caused by lack of power. We considered applying formal corrections for multiple comparisons, but decided not to, because the results were consistent  with multiple comparisons pointing towards the same conclusion (illustrated by Figs 1 and 2), and to avoid type II errors. Lack of power may explain the absence of associations between the degree of thyroid dysfunction and HRQL, as e.g. only 12 patients had overt hypothyroidism at baseline. Finally, although hypothyroidism–also when adequately treated–is associated with increased morbidity and mortality [32–34], we cannot rule out that HRQL issues would have improved further with longer follow-up. Extended follow-up could also have helped to unmask a potential response bias of participants knowingly being started on LT4. Disfavoring such a bias, the improvements at six weeks were, with one exception, consistent at six months.
Despite the limitations mentioned, our data can help clinicians inform hypothyroid patients what to expect, when starting on LT4 therapy. Benefits of addressing the patient perspective in medical communication are well established  and future studies should investigate whether HRQL assessment in clinical practice can improve the care for hypothyroid patients . Recent investigations encourage initiatives that stimulate ethical placebo mechanisms in clinical practice. HRQL assessment could do so by contributing, in a positive manner, to the overall therapeutic context . To advance its applicability, both in clinical practice and research, we have recently developed a short version of ThyPRO . It constitutes the primary outcome in our on-going randomized controlled trial of selenium supplementation in AIT , and can be put to ideal use in future trials investigating various formulations of LT4 and/or combinations with liothyronine  or placebo-controlled trials in subclinical hypothyroidism .
In conclusion, untreated hypothyroid patients experience widely impacted HRQL, compared to the general population. Most aspects improve during the first six months of LT4 therapy but some deficits remain, including tiredness, which is the cardinal manifestation. Whether full remission in HRQL, with this or any combination of LT4 and liothyronine, will ensue with longer follow-up remains to be explored.
We thank the staff and colleagues at the Departments of Endocrinology at Rigshospitalet and Odense University Hospital. Special thanks to our research assistant, Sofie Larsen Rasmussen, for her assistance with collection of HRQL surveys and clinical data entry. Finally, we thank the patients who participated in the study, and the respondents who served as a normal reference population.
Researchers who want to use the ThyPRO may contact Torquil Watt (Torquil.Watt@regionh.dk).
Conceived and designed the experiments: TW JBB UFR MG AKR LH SJB. Performed the experiments: PC TW UFR AKR LH SJB. Analyzed the data: KHW PC TW. Contributed reagents/materials/analysis tools: OE. Wrote the paper: KHW PC TW JBB OE UFR MG AKR LH SJB.
- 1. Pedersen IB, Laurberg P, Knudsen N, Jørgensen T, Perrild H, Ovesen L, et al. An increased incidence of overt hypothyroidism after iodine fortification of salt in Denmark: a prospective population study. J Clin Endocrinol Metab 2007; 92:3122–3127. pmid:17504896
- 2. Carle A, Laurberg P, Pedersen IB, Knudsen N, Perrild H, Ovesen L, el al. Epidemiology of subtypes of hypothyroidism in Denmark. Eur J Endocrinol 2006; 154:21–28. pmid:16381987
- 3. Wiersinga WM. Paradigm shifts in thyroid hormone replacement therapies for hypothyroidism. Nat Rev Endocrinol 2014; 10:164–174. pmid:24419358
- 4. Saravanan P, Chau WF, Roberts N, Vedhara K, Greenwood R, Dayan CM. Psychological well-being in patients on 'adequate' doses of l-thyroxine: results of a large, controlled community-based questionnaire study. Clin Endocrinol (Oxf) 2002; 57:577–585.
- 5. Wekking EM, Appelhof BC, Fliers E, Schene AH, Huyser J, Tijssen JG, et al. Cognitive functioning and well-being in euthyroid patients on thyroxine replacement therapy for primary hypothyroidism. Eur J Endocrinol 2005; 153:747–753. pmid:16322379
- 6. Quinque EM, Villringer A, Kratzsch J, Karger S. Patient-reported outcomes in adequately treated hypothyroidism—insights from the German versions of ThyDQoL, ThySRQ and ThyTSQ. Health Qual Life Outcomes 2013; 11:68. pmid:23618009
- 7. Kelderman-Bolk N, Visser TJ, Tijssen JG, Berghout A. Quality of life in patients with primary hypothyroidism is related to BMI. Eur J Endocrinol 2015; 173: 507–515. pmid:26169304
- 8. Black N. Patient reported outcome measures could help transform healthcare. BMJ 2013; 346:f167 pmid:23358487
- 9. Guyatt GH, Feeny DH, Patrick DL. Measuring health-related quality of life. Ann Intern Med 1993; 118:622–629. pmid:8452328
- 10. Hays RD. Generic versus disease-targeted instruments. In: Fayers P, Hays RD (eds). Assessing quality of life in clinical trials. 2nd edition. Oxford University Press, Oxford, 2005; 3–8.
- 11. Ware JE Jr., Sherbourne CD. The MOS 36-item short-form health survey (SF-36). I. Conceptual framework and item selection. Med Care 1992; 30:473–483. pmid:1593914
- 12. Contopoulos-Ioannidis DG, Karvouni A, Kouri I, Ioannidis JP. Reporting and interpretation of SF-36 outcomes in randomised trials: systematic review. BMJ 2009; 338:a3006. pmid:19139138
- 13. McMillan CV, Bradley C, Woodcock A, Razvi S, Weaver JU. Design of new questionnaires to measure quality of life and treatment satisfaction in hypothyroidism. Thyroid 2004; 14:916–25. pmid:15671770
- 14. McMillan CV, Bradley C, Razvi S, Weaver JU. Evaluation of new measures of the impact of hypothyroidism on quality of life and symptoms: the ThyDQoL and ThySRQ. Value Health 2008;11:285–294. pmid:18380641
- 15. Watt T, Hegedus L, Rasmussen AK, Groenvold M, Bonnema SJ, Bjorner JB, et al. Which domains of thyroid-related quality of life are most relevant? Patients and clinicians provide com-plementary perspectives. Thyroid 2007; 17:647–54. pmid:17696835
- 16. Watt T, Rasmussen AK, Groenvold M, Bjorner JB, Watt SH, Bonnema SJ, et al. Improving a newly developed patient-reported outcome for thyroid patients, using cognitive interviewing. Qual Life Res 2008; 17:1009–17. pmid:18584308
- 17. Watt T, Bjorner JB, Groenvold M, Rasmussen AK, Bonnema SJ, Hegedüs L, et al. Establishing construct validity for the thyroid-related patient reported outcome measure (ThyPRO): an initial examination. Qual Life Res 2009; 18:483–96. pmid:19288224
- 18. Watt T, Hegedus L, Groenvold M, Bjorner JB, Rasmussen AK, Bonnema SJ, et al. Validity and reliability of the novel thyroid-specific quality of life questionnaire, ThyPRO. Eur J Endocrinol 2010; 162:161–167 pmid:19797502
- 19. Watt T, Groenvold M, Hegedus L, Bonnema SJ, Rasmussen AK, Feldt-Rasmussen U, et al. Few items in the thyroid-related quality of life instrument ThyPRO exhibited differential item functioning. Qual Life Res 2014; 23: 327–338. pmid:23812962
- 20. Watt T, Groenvold M, Deng N, Gandek B, Feldt-Rasmussen U, Rasmussen AK, et al. Confirmatory factor analysis of the thyroid-related quality of life questionnaire ThyPRO. Health Qual Life Outcomes 2014; 12:126. pmid:25213857
- 21. Watt T, Cramon P, Hegedus L, Bjorner JB, Bonnema SJ, Rasmussen AR, et al. The thyroid-related quality of life measure ThyPRO has good responsiveness and ability to detect relevant treatment effects. J Clin Endocrinol Metab 2014; 99:3708–3717. pmid:25004246
- 22. Ware JE Jr., Kosinski M, Bjorner JB, Maruish M. 2007 SF-36 Health Survey. Manual and Interpretation Guide. 2nd edition, QualityMetric Incorporated, Lincoln, RI.
- 23. Cramon P, Bonnema SJ, Bjorner JB, Ekholm O, Feldt-Rasmussen U, Frendl DM, et al. Quality of life in patients with benign nontoxic goiter: impact of disease and treatment response, and comparison with the general population. Thyroid 2015; 25:284–91. pmid:25602312
- 24. Ekholm O, Hesse U, Davidsen M, Kjoller M. The study design and characteristics of the Danish national health interview surveys. Scand J Public Health 2009; 37:758–765. pmid:19622549
- 25. Cohen J. A power primer. Psychol Bull 1992; 112:155–159. pmid:19565683
- 26. Carle A, Pedersen IB, Knudsen N, Perrild H, Ovesen L, Laurberg P. Hypothyroid symptoms and the likelihood of overt thyroid failure: a population-based case-control study. Eur J Endocrinol 2014;171:593–602. pmid:25305308
- 27. Samuels MH. Psychiatric and cognitive manifestations of hypothyroidism. Curr Opin Endocrinol Diabetes Obes 2014; 21:377–83. pmid:25122491
- 28. Dayan CM, Panicker V. Hypothyroidism and depression. Eur Thyroid J 2013; 2:168–79. pmid:24847450
- 29. Krysiak R, Drosdzol-Cop A, Skrzypulec-Plinta V, Okopien B. Sexual function and depressive symptoms in young women with thyroid autoimmunity and subclinical hypothyroidism. Clin Endocrinol 2015; [Epub ahead of print]
- 30. Canaris GJ, Manowitz NR, Mayor G, Ridgway EC. The Colorado thyroid disease prevalence study. Arch Intern Med 2000;160:526–34. pmid:10695693
- 31. Ridker PM, Danielson E, Fonseca FA, Genest J, Gotto AM Jr., Kastelein JJ, et al. Rosuvastatin to prevent vascular events in men and women with elevated C-reactive protein. New Engl J Med 2008;359:2195–2207. pmid:18997196
- 32. Thvilum M, Brandt F, Almind D, Christensen K, Hegedus L, Brix TH. Excess mortality in patients diagnosed with hypothyroidism: a nationwide cohort study of singletons and twins. J Clin Endocrinol Metab 2013; 98:1069–1075. pmid:23365121
- 33. Thvilum M, Brandt F, Almind D, Christensen K, Brix TH, Hegedus L. Type and Extent of Somatic Morbidity before and after the Diagnosis of Hypothyroidism. A Nationwide Register Study. PloS One 2013; 8:e75789. pmid:24066186
- 34. Thvilum M, Brandt F, Almind D, Christensen K, Brix TH, Hegedüs L. Increased Psychiatric Morbidity Before and After the Diagnosis of Hypothyroidism: A Nationwide Register Study. Thyroid 2014; 24:802–808. pmid:24383722
- 35. Stewart M, Brown JB, Donner A, McWhinney IR, Oates J, Weston WW, et al. The impact of patient-centered care on outcomes. J Fam Pract 2000; 49:796–804. pmid:11032203
- 36. Tzelepis F, Sanson-Fisher RW, Zucca AC, Fradgley EA. Measuring the quality of patient-centered care: why patient-reported measures are critical to reliable assessment. Patient Prefer Adherence 2015; 9:831–835. pmid:26150703
- 37. Finniss DG, Kaptchuk TJ, Miller F, Benedetti F. Biological, clinical, and ethical advances of placebo effects. Lancet 2010; 375:686–95. pmid:20171404
- 38. Watt T, Bjorner JB, Groenvold M, Cramon P, Winther KH, Hegedus L, et al. Development of a short version of the thyroid-related patient-reported outcome ThyPRO. Thyroid 2015; 25:1069–1079. pmid:26214034
- 39. Winther KH, Watt T, Bjorner JB, Cramon P, Feldt-Rasmussen U, Gluud C, et al. The chronic autoimmune thyroiditis quality of life selenium trial (CATALYST): study protocol for a randomized controlled trial. Trials 2014; 15:115. pmid:24716668